research papers\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

IUCrJ
Volume 12| Part 6| November 2025| Pages 658-669
ISSN: 2052-2525

X-ray electron density analysis of chemical bonding in permanent magnet Nd2Fe14B

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aCenter for Integrated Materials Research, Department of Chemistry and iNANO, Aarhus University, Langelandsgade 140, 8000 Aarhus, Denmark
*Correspondence e-mail: [email protected]

Edited by A. Fitch, ESRF, France (Received 12 May 2025; accepted 25 August 2025; online 29 September 2025)

Chemical bonding determines the intrinsic properties of materials, but despite the super-strong metallic magnet Nd2Fe14B being a vital compound in modern life, the local chemical environment is not well understood. Nd2Fe14B has a very complex crystal structure with six independent Fe sites, two independent Nd sites and one B site, which in concert are responsible for the extremely high magnetic moment. Dense inorganic materials with excellent crystal quality and heavy atoms represent a strong challenge to X-ray charge density analysis, and indeed Nd2Fe14B has a mere suitability factor of 0.02 compared with 3–5 for typical organic molecular crystals. Here, we report high-energy (λ = 0.2482 Å) 25 K single-crystal synchrotron X-ray diffraction data suitable for multipole modelling of the X-ray charge density. The X-ray electron density shows local anisotropy in the bonding environment of the Fe atoms, and topological analysis quantifies that the Nd atoms are positive (∼+1), one Fe atom and B are negative (−1.7 and −0.44, respectively), and the remaining Fe atoms are close to neutral (±0.1). The d orbitals of all Fe atoms are close to being evenly populated, and bonding analysis establishes a multidirectional `metal-like' framework. It is found that a single Fe atom is crucial for the 3D framework of the magnetic structure. Through structural refinement of synchrotron single-crystal X-ray diffraction data at 25 K, 100 K, 200 K and 300 K, anisotropic displacement parameters are obtained, and the Debye temperature is estimated to be 345–383 K.

1. Introduction

Magnets are omnipresent in modern society from engines to electronics and much in between. The discovery of the super-strong magnet Nd2Fe14B in 1982 revolutionized magnetic research (Croat et al., 1984View full citation; Sagawa et al., 1984View full citation), and still today it has the highest known energy product. It is produced on a large scale and applications span from windmills to electrical cars – it is an essential material for the green transition (Hioki, 2021View full citation; Wu et al., 2018View full citation). Following the discovery, the crystal structure was established by single-crystal X-ray diffraction (SCXRD) in 1984 (Shoemaker et al.; 1984View full citation), but since then research has largely focused on technological applications and less on understanding the complex atomic structure fundamentally responsible for the outstanding properties. It is striking that no studies so far have concerned the basic electronic structure of the material. It is the nature of the chemical bonding between atoms that induces the specific properties of a material, but for Nd2Fe14B there is an absence of the chemical bonding analysis which otherwise often drives modern materials development. The reasons for this knowledge gap are probably many, but one is the complexity of the crystal structure where the unit cell contains 68 open-shell atoms making accurate theoretical modelling extremely challenging due to numerous closely spaced energy states. At this point there is limited insight into the fundamental chemical interactions and atomic properties of Nd2Fe14B.

The electronic structure of a crystalline material can be obtained theoretically, e.g. through periodic density functional theory calculations (Gu & Ching, 1987View full citation), and experimentally the crystal electron density can be determined from modelling of very accurate high-resolution X-ray diffraction data (Stokkebro Schmøkel, Overgaard & Brummerstedt Iversen, 2013View full citation). For X-ray diffraction the dense heavy atom nature leads to substantial absorption and extinction effects in the data, but such challenges may be overcome using high-energy synchrotron radiation and small crystal specimens coupled with very low temperature measuring conditions (Tolborg & Iversen, 2019View full citation). Helium cooling allows data to be recorded to very high resolution due to limited thermal damping of the high-order intensity. High-order data are vital for separating valence electron effects from thermal motion effects (Iversen et al., 1999View full citation). However, the more fundamental challenge is that the scattering signal from the relatively few valence electrons is very weak compared with the signal from the electron-rich atomic cores. This puts strong demands on the accuracy of the data if the chemical bonding (valence electrons) is to be studied. The suitability factor quantifies the ratio between valence electrons and core electrons, and for typical organic molecular crystals it has a value of 3–5 (Stevens & Coppens, 1976View full citation). For extended inorganic solids previously studied by X-ray electron density analysis such as TiS2 (Kasai et al., 2018View full citation), CoSb3 (Stokkebro Schmøkel, Bjerg et al., 2013View full citation), FeSb2 (Grønbech et al., 2020View full citation) and ZnSb (Grønbech et al., 2024View full citation) it is 0.01–0.1, whereas for Nd2Fe14B the suitability has a value of 0.02. The crystal complexity and heavy-atom nature of Nd2Fe14B possibly makes this the most difficult X-ray electron density study so far. To succeed we first embarked on synthesis of very high quality single crystals using the Czochralski technique, and then collected X-ray diffraction data at 25 K using high-energy X-rays from the SPring8 synchrotron in Japan.

2. Experimental

2.1. Synthesis

For growth, a 17.4 g sample composed of 51 at% Nd, 44 at% Fe and 5 at% B (Susner et al., 2017View full citation) was loaded into a pyrolytic BN crucible which was placed in a graphite susceptor. Before loading the BN crucible, the oxide layer which had formed on top of the Nd was scratched off. The graphite susceptor was placed in a copper coil with five windings which was placed in an ADL-type induction furnace. The furnace was evacuated to ∼2 × 10−2 mbar and filled with He to ambient pressure five times before being pressurized to 200 psi with He. The samples were heated to ∼1200°C and left to homogenize for 30 min after melting to ensure an even distribution of all elements throughout the melt. The crucible was rotated at 1.5 rpm to give a better heat distribution throughout the melt. After homogenization a tungsten wire was lowered into the melt and a Czochralski pull was begun with a pulling rate of ∼8 mm h−1. The growth was carried out and a rod with a length of ∼3 cm was obtained. During the growth, some impurity was observed to be present on top of the melt. This impurity is believed to originate from some oxidation of Nd before the inert atmosphere was established; the impurities were not believed to have affected the growth as rotation of the crucible ensured that the impurities were pushed towards the crucible edge. The rod was removed from the furnace and submerged in oil in order to avoid oxidation of the grown crystal. Submersion in oil was chosen as some light coloration was observed on the outside of the crystal. It is unknown whether this coloration arose from some of the impurities observed on the melt during growth or from oxidation of the rod after exposure to ambient air. To obtain a crystal for SCXRD measurements, the rod was snapped in two pieces. A sharp razor was used to apply pressure to the newly exposed surface to scrape off crystallites. The crystallites were transferred to a glass slide and covered in oil to avoid oxidation.

2.2. SCXRD measurements

Data were measured on a 25 µm × 60 µm × 130 µm crystal at SPring-8 at the BL02B1 beamline using a wavelength of 0.2482 Å. Datasets were collected at 300 K, 200 K, 100 K and 25 K using liquid N2/He cryostats to control the temperature. The beamline is equipped with a quarter χ goniometer and a Pilatus3 X 1M CdTe detector (Krause et al., 2020View full citation). For the 300 K, 200 K and 100 K data, three 180° ω scans were collected at χ values of 0°, 25° and 45° for a 2θ value of 0°. For the 300 K dataset an exposure time of 0.5 s/frame was used while for the 200 K and 100 K an exposure time of 0.25 s was used. A scan width of 0.1°/frame was used resulting in a total of 5400 frames collected for each of the three temperatures. A low-angle 25 K dataset was collected with the same strategy as the 200 K and 100 K datasets, with an additional full 180° ω scan in the χ = 0° setting (1800 extra frames) and the first 90° of the ω scan for χ = 25° (900 frames). To obtain a higher resolution a high-angle dataset was collected at 25 K with χ values of 0°, 25° and 45° and a 2θ value of 20°, resulting in a total of 13500 frames collected at 25 K. Data obtained from SPring8 were converted to Bruker format using the Pilatus3 frame conversion software developed by Krause (https://github.com/LennardKrause/). Data reduction was performed in the APEX5 GUI for the program SAINT (Bruker, 2019View full citation) with the recurrence background setting. SADABS (Krause et al., 2015View full citation) was used for scaling and absorption correction (μ = 4.3, μr = 0.15) of the integrated data. The isotropic absorption correction factor, μr, is calculated from the tabulated linear absorption coefficient, μ = 4.3 mm−1 [calculated as an average of the FPRIME and BRENNAN values from WinGX (Farrugia, 2012View full citation)] and a projected isotropic radius (r = 0.035 mm−1) estimated by equating the crystal block volume to the volume of a sphere. Two datasets were obtained for low- and high-angle data at 25 K. The SORTAV (Blessing, 1997View full citation) program was used for merging the two datasets, as well as rejection of outliers, merging of the equivalent reflections and to obtain estimates of their uncertainties. Reflections with d-spacing higher than dmax = 4 Å (sin θ/λmin = 0.125 Å−1) were rejected, due to only partial detection, as they were hidden by the beam stop shadow or hit spaces between detector panels [in total 6 reflections: (101), (110), (002), (111), (200) and (112)]. An initial estimate of the resolution limit was dmin = 0.27 Å (sin θ/λmax = 1.85 Å−1) since significant reflections were available to this limit, but the resolution was later reduced to dmin = 0.33 Å (sin θ/λmax = 1.5 Å−1) for better reflection statistics. For the datasets at 100 K, 200 K and 300 K all reflections until a resolution of dmin = 0.4 Å (sin θ/λmax = 1.25 Å−1) were used.

2.3. Structure solution and IAM refinement

The structure was solved and refined using SHELXT (Sheldrick, 2015aView full citation) and SHELXL (Sheldrick, 2008View full citation; Sheldrick, 2015bView full citation) in Olex2 (Dolomanov et al., 2009View full citation). The independent atom model (IAM) structure included free refinement of atomic coordinates and anisotropic atomic displacement parameters (ADPs), up to nine parameters per atom (x, y, z and six Uij ADPs) when allowed by the site symmetry. All occupancies refined to 1 within ±0.001 and were fixed to 1.0. Crystallographic information is given in Table 1[link].

Table 1
Crystallographic information for Nd2Fe14B in the tetragonal space group P42/mnm with Z = 4

Values for the 25 K dataset are given for the MM from XD2016 (Volkov et al., 2016View full citation), while the others are for the IAM in Olex2 (Dolomanov et al., 2009View full citation). The definition of parameters varies slightly and should therefore not be compared between programs.

  Temperature (K)
  25 100 200 300
a, c (Å) 8.8128 (2), 12.1904(3) 8.8135 (2), 12.1933 (3) 8.81530 (14), 12.2028 (2) 8.8143 (2), 12.2117 (2)
V3) 946.77 (5) 947.15 (5) 948.27 (3) 948.75 (5)
Measured, independent reflections 371711, 7099 143660, 4151 143509, 4167 142676, 4168
Rint, multiplicity, completeness (%) 0.046, 42.4, 99.9 0.042, 34.5, 100.0 0.047, 34.4, 100.0 0.037, 34.2, 100.0
R(F2), wR(F2), GooF 0.014, 0.030, 1.00 0.009, 0.021, 1.12 0.009, 0.022, 1.07 0.008, 0.020, 1.13
Δρmax, Δρmin (e Å−3) 1.25, −2.13 0.88, −2.50 0.75, −2.31 0.62, −1.75
†The minute reduction observed for the a lattice parameter from 200 K to 300 K is attributed to the relatively lower experimental precision in unit-cell determination by SCXRD.

2.4. Multipole modelling

For electron density analysis a multipole model (MM) was refined in XD2016 (Volkov et al., 2016View full citation) against the merged 25 K dataset using the Volkov & Macchi (unpublished work) databank for radial functions. Only the valence electrons were allowed to deform in the multipoles, so the following choice of valence was made: the outermost s and f electrons (6s24f4) were considered valence for Nd, for Fe the two 4s electrons were given a separate monopole and κ, and the six 3d electrons were allowed to deform, while the 2s and 2p electrons were considered valence for B. The lanthanides are usually found in their +III oxidation state, but since no obvious charge count for the remaining ions would balance this, all atoms were kept neutral in the initial model. All symmetry-allowed multipoles up to the hexadecapole level (lmax = 4) were allowed to refine along with atomic coordinates and anisotropic ADPs. A test for anharmonic motion on Nd and Fe was performed, but due to low significance, high correlation with harmonic vibrational parameters (>80%) and no improvement in quality parameters it was deemed irrelevant for the model. For a better description of Nd, a separate κ and a dipole were refined for the outermost orbitals of the Nd core, specifically the diffuse 4d10 and 5s25p6 (see the supporting information). In the final model, the κ parameters were fixed and the scale factor was manually optimized (reduced by ∼0.2%) (Meindl & Henn, 2008View full citation), accounting for an insufficient correction for absorption and/or anomalous dispersion correction of the Nd atoms (Meurer et al., 2024View full citation). Attempts to model the 4f electrons on Nd explicitly using multipoles up to the lmax = 6 level in Jana2020 (Petříček et al., 2023View full citation) gave no improvements to the model, so the XD2016 lmax = 4 model was used for further analysis (see discussion in the supporting information).

The κ values were 1.049/1.026 for the Nd valence/core, 1.046/1.006 for Fe 3d/4s valence and 0.990 for B. The largest correlation coefficient between parameters was 0.80 between the core and valence dipole on Nd. The highest peaks (1.25 e Å−3 and 1.08 e Å−3) and deepest holes (−2.13 e Å−3 and −1.17 e Å−3) in the residual density were found at a distance less than 0.5 Å from Nd1 and Nd2, respectively, suggesting an incomplete description of the density in the vicinity of the Nd atoms. The largest residuals on Fe atoms are 0.70 e Å−3 0.5 Å from Fe6 and −1.04 e Å−3 0.5 Å from Fe4. Fig. 1[link](a) shows a systematic narrowing of the fractal dimension plot when comparing the IAM and MM. The normal probability plot in Fig. 1[link](b) shows no systematic changes, while the F2obs/F2calc plot in Fig. 1[link](c) shows improvements for the low-angle reflections (sin θ/λ < 0.4 Å−1), as expected for a better description of the valence deformation in the MM.

[Figure 1]
Figure 1
(a) Fractal dimension plot, (b) normal probability plot [δR = (F2obsF2calc)/σ(F2)], and (c) F2obs/F2calc plot for the MM (red) and IAM (grey) of Nd2Fe14B.

From the residual density maps of the IAM [Figs. 2[link](a) and 2[link](c)] and MM [Figs. 2[link](b) and 2[link](d)] in the (001) and (110) planes in Fig. 2[link], it is apparent that the residuals near the atomic sites significantly improve in the MM. The residual density provides the discrepancy between the observed and modelled density, and the improvement is seen by a pronounced reduction in the extent, as well as height and depth of the residuals (number of contour lines) in the vicinity of atomic centres. For example, a deep hole is placed near Nd1, seen as an excessive number of negative (red) contours in the IAM [Fig. 2[link](a)], a feature which is much shallower in the MM [Fig. 2[link](b)]. Similarly, a positive (blue) feature near Nd2 in the IAM [three contours in Fig. 2[link](a)] is almost eliminated in the MM [one contour in Fig. 2[link](b)], while also the extent and depth of the negative (red) contours are significantly reduced. The same is seen for the Fe atoms in Figs. 2[link](c)–2[link](d), where e.g. Fe3 shows a shift from five red contours in the IAM to only two red contour lines in the MM, and the positive–negative–positive feature at Fe4 in the IAM is eliminated to only exhibit reduced negative residuals in the MM. Importantly, the MM allows for extraction of the electron density for analysis.

[Figure 2]
Figure 2
Residual density maps of Nd2Fe14B in the (a)–(b) (001) and (c)–(d) (110) planes of the unit cell. (a) and (c) show the IAM, and (b) and (d) show the MM. The resolution is truncated at 0.7 Å−1 to emphasize valence scattering. Positive (blue), negative (red) and zero (black) contours are shown at the 0.1 e Å−3 level.

3. Results and discussion

3.1. Structure and ADPs

Nd2Fe14B (M = 1081 g mol−1) crystallizes in the tetragonal space group P42/mnm, with unit-cell parameters a = 8.8143 (2) Å and c = 12.2117 (2) Å at 300 K, and four formula units in the unit cell. Note that a spin-reorientation phase transition happens at 135 K resulting in a monoclinic magnetic space group Cm to account for a 37° tilted magnetic moment. Here we report the structure at four temperatures (25 K, 100 K, 200 K and 300 K) of a non-magnetized sample below the Curie temperature of 585 K (Sagawa et al., 1984View full citation). In this 275 K temperature range the unit cell shows linear, though minute, changes of less than 1% increase in volume, and linear expansion coefficients of 0.8 (5) × 10−6 K−1 and 6.6 (7) × 10−6 K−1 along the a and c directions, respectively. This is consistent with Herbst et al. (1985View full citation) observing significant unit-cell changes only above the Curie temperature.

The asymmetric unit contains nine atoms: Nd1 (Wyckoff site: 4f), Nd2 (4g), Fe1 (4e), Fe2 (4c), Fe3 (8j), Fe4 (8j), Fe5 (16k), Fe6 (16k) and B1 (4f). The reported unit cell and atomic positions (Table 2[link]) are consistent with Herbst et al. (1984View full citation) (a = 8.80 Å, c = 12.19 Å) and Shoemaker et al. (1984View full citation) [a = 8.804 (5) Å and c = 12.205 (5) Å]. Atomic positions are in excellent agreement with Shoemaker et al. (1984View full citation) for Nd and Fe differing only on the fourth decimal, while B coordinates differ by 0.002.

Table 2
Atomic positions and Beq at 300 K

Coordinates are reported for positions equivalent with Table 1 in Shoemaker et al. (1984View full citation) and Beq is derived from Uij as Beq = 8π2Ueq, where Ueq = (U11 + U22 + U33)/3 for an easier comparison. Unit-cell transformation: rotation: (0, 1, 0; −1, 0, 0; 0, 0, 1) and translation: (0, 0, 1/2).

  x, y, z Beq2)
Nd1 0.14309 (2), 0.14309 (2), 0.00000 0.5266 (8)
Nd2 0.72978 (2), 0.27022 (2), 0.00000 0.5140 (8)
Fe1 0.00000, 0.00000, 0.38499 (2) 0.4358 (8)
Fe2 0.00000, 0.50000, 0.000000 0.4911 (8)
Fe3 0.40196 (2), 0.40196 (2), 0.29525 (2) 0.5085 (8)
Fe4 0.18254 (2), 0.18254 (2), 0.25424 (2) 0.5132 (8)
Fe5 0.72459 (2), 0.06700 (2), 0.37236 (2) 0.4887 (8)
Fe6 0.46308 (2), 0.13995 (2), 0.32395 (2) 0.4564 (8)
B1 0.37563 (7), 0.37563 (7), 0.00000 0.658 (7)

Of the 31 entries for Nd2Fe14B with the P42/mnm space group at 300 K in the ICSD, only four report isotropic (Biso) or anisotropic (Bij or Beq) vibrational parameters that are different to Biso = 1. Beq's for the structure presented here can be seen in Table 2[link], and Fig. 3[link] shows a comparison of the reported ADPs for Nd2Fe14B in the ICSD. Shoemaker et al. (1984View full citation) refined separate Bij's for all Nd and Fe, and Biso for B, with the same relative behaviour as the present study, while slightly overestimating the vibrations (on average 10% for Nd and Fe, and >100% for B). Herbst et al. (1985View full citation) refined one common Biso for Nd and Fe, and one for B, overestimating the vibrations for all atoms, while Isnard et al. (1995View full citation) underestimated the vibrations of Nd and Fe by refining one Biso for each type of atom, and fixed Biso = 1.2 Å2 for B. Liao et al. (1993View full citation) refined Biso's for all atoms, but gave no uncertainties for the parameters. In general, the B vibrations are heavily overestimated by a factor of 2–3.

[Figure 3]
Figure 3
Isotropic or equivalent vibrational parameters (Biso/eq) as reported by Liao et al. (1993View full citation) (ICSD code 41393), Herbst et al. (1985View full citation) (ICSD code 44294), Shoemaker et al. (1984View full citation) (ICSD code 48143), Isnard et al. (1995View full citation) (ICSD code 80971) and the 300 K structure in this study. The dotted grey line shows the commonly used Biso = 1.0 line.

The evolution of vibrational parameters (Uij) from 25 K to 300 K for each atom in the asymmetric unit can be seen in Fig. 4[link] along with calculated values for Ueq. The Debye temperature (θD) for each atom was calculated from the integral form of the Debye model fitted against Ueq data points from 25 K to 300 K (Willis & Pryor, 1975View full citation), as

Mathematical equation

where ℏ is 1/2π times the Plank constant; kB is the Boltzman's constant; and m represents the atomic masses of 144.242 g mol−1, 55.845 g mol−1 and 10.811 g mol−1 for Nd, Fe and B, respectively. d2 is a term to describe the potential static disorder components of the ADP (Bentien et al., 2005View full citation). Nd shows the lowest Debye temperature of ∼220 K. The average value for Fe is 375 K, while B has a much higher Debye temperature than the other atoms of 752 (11) K, as expected due to tighter bonding and a more rigid local framework surrounding B.

[Figure 4]
Figure 4
Vibrational parameters (Uij) for the nine atoms in the asymmetric unit. The full lines show Ueq while the shaded lines show vibrations along each of the principal axes of the ellipsoid. The dotted black line is the model fit to the 25–300 K Ueq data points. Some directions are restricted by the site symmetry. Debye temperatures in Kelvin are given for each atom.

Fits to individual atom ADPs is not the intended use of the Debye model developed for a monoatomic cubic lattice, but still provides some insights into the thermal behaviour of each atom in the material (Willis & Pryor, 1975View full citation; Bentien et al., 2005View full citation). For a polyatomic solid there is no straightforward way of calculating the material's Debye temperature, but two attempts have been made here. Values of 345 (2) K and 383 (3) K are obtained from (1) the average of the mass-weighted Ueq's and (2) the average of the Debye temperatures. The values determined from the ADPs are somewhat lower than the Debye temperature reported from heat capacity measurements of 418 (12) K (Morishita et al., 2020View full citation).

3.2. Extended structure/bonding features/frameworks

The unit cell, seen in Fig. 5[link], consists of alternating Fe and Nd/B layers. The description of the structure given here is inspired by the interpretation by others (Herbst et al., 1985View full citation; Grin et al., 2007View full citation). B1 forms distorted trigonal prisms with Fe1 and Fe5 in the vertices [green polyhedra in Fig. 5[link](a)]. Fe1/Fe3/Fe5/Fe6 form a triangular-hexagonal layer at z ≃ 1/3 (thickness in z < 0.1) with bond lengths of approximately 2.5 Å, shown in Fig. 5[link](b). Fe4 is placed in the z = 1/4 plane between two triangular-hexagonal layers in z ≃ 1/6 and z ≃ 1/3 with slightly longer bond lengths of 2.7 Å to each layer. The triangular-hexagonal layers have two types of hexagons (containing the atoms: Fe3/Fe5/Fe6 and Fe1/Fe3/Fe5/Fe6). Each Fe4 coordinates to two hexagons of different types in the layers above and below as shown in Figs. 5[link](b) and 5[link](i). The two triangular-hexagonal sandwich layers are related by a 90° rotation and a translation of 1/2 along the ab diagonal. Together each triangular-hexagonal layer forms a slightly distorted trigonal framework with Fe4. Fe2 is placed in the Nd/B layer symmetrically coordinating to 8 Fe atoms (two Fe5 and two Fe6 below and above the z plane) linking two trigonal Fe sandwich frameworks, as shown in Fig. 5[link](a). All interatomic vectors between Nd and Fe have a low difference of mean-square displacement amplitude (DMSDA) on the order of 10−4 Å2 while bonds with B, as expected, have one order of magnitude higher DMSDA. The bond lengths are in good agreement with Herbst et al. (1985View full citation) and Shoemaker et al. (1984View full citation).

[Figure 5]
Figure 5
Unit cell along the (a) a and (b) c directions. Grey lines highlight the triangular-hexagonal Fe1/Fe3/Fe5/Fe6 layers with Fe4 in between and the Fe2 coordination. Green trigonal prisms show coordination of B. (c)–(k) Coordination environments of all symmetry-independent atoms visualized along the a direction. Thin grey lines show the first coordination sphere (within 3.8 Å), black lines show bonding contacts confirmed by the presence of BCPs at 25 K. The 300 K structure is used for visualization with thermal ellipsoids shown at a 99% probability level. Figures were drawn using Vesta (Momma & Izumi, 2008View full citation).

3.3. Bonding analysis and electron density

Electron density analysis is a powerful tool to determine and categorize chemical bonds in crystals from diffraction data (Coppens, 1997View full citation). Chemical bonds and other topological features are well defined within the quantum theory of atoms in molecules (QTAIM) (Bader, 1994View full citation). Bond critical points (BCPs) and their properties can be found in Table 3[link]. Only few have attempted modelling the electron density of lanthanide and actinide compounds (Eu, Gd, Tb, Dy, Th, U) and generally the f-block element is found surrounded by much less electron-rich ligands in a metal–organic complex (Iversen et al., 1998View full citation; Iversen et al., 1999View full citation; Gianopoulos et al., 2017View full citation; Gianopoulos et al., 2019View full citation; Zhurov, Zhurova & Pinkerton, 2011View full citation; Zhurov, Zhurova, Stash & Pinkerton, 2011View full citation; Gao et al., 2020View full citation; Ananyev et al., 2016View full citation; Puntus et al., 2008View full citation). Exact determination of the coordination number of atoms in especially polyatomic solids is troublesome and depends on several assumptions and definitions. Here the presence of a BCP shared between two atoms is considered a point of interaction and will be noted as a bond. A more rigid discussion about the chemical implications of BCPs, bond paths and the presence of shared interatomic surfaces between atoms in the topological framework has recently been given elsewhere (Wagner et al., 2025View full citation).

Table 3
Bond critical points (BCPs) and their properties as determined by topological analysis of the electron density

Derived properties are calculated from the density, ρ, and Laplacian, ∇2ρ, using the Abramov approximation and the virial theorem for the kinetic energy, G, and potential energy, V, respectively (Gatti, 2005View full citation). The unit H is Hartree. Uncertainties on ρ and ∇2ρ are ±0.001 as estimated by XD2016, while uncertainties on the energies found by propagation of error are on the second decimal. These values are much lower than typical systematic errors in the X-ray electron density analysis (Shi et al., 2019View full citation).

    ρb (e Å−3) 2ρb (e Å−5) Rij (Å) ɛ Gb (H Å−3) Vb (H Å−3) Hb (H Å−3) Hb/ρb |Vb|/Gb
Nd1 Nd1i 0.095 0.468 3.566 0.84 0.04 −0.04 0.00 −0.05 1.13
  B1 0.221 1.613 2.904 0.22 0.14 −0.17 −0.03 −0.12 1.19
  Fe4 0.168 1.016 3.137 0.09 0.09 −0.11 −0.02 −0.10 1.20
Nd2 Fe1ii 0.132 0.799 3.197 1.19 0.06 −0.07 −0.01 −0.07 1.14
B1 Fe1 0.464 3.401 2.095 0.06 0.38 −0.53 −0.14 −0.31 1.38
  Fe5iii 0.528 3.588 2.110 0.04 0.44 −0.64 −0.19 −0.37 1.44
Fe1 Fe4iii 0.225 1.085 2.787 0.1 0.12 −0.16 −0.04 −0.18 1.35
  Fe3 0.282 1.928 2.516 0.18 0.19 −0.24 −0.05 −0.19 1.28
Fe2 Fe5iv 0.229 1.530 2.597 0.31 0.14 −0.17 −0.03 −0.15 1.24
  Fe6 0.260 1.965 2.498 0.02 0.18 −0.22 −0.04 −0.15 1.22
Fe3 Fe3v 0.337 1.911 2.444 0.1 0.22 −0.31 −0.09 −0.26 1.39
  Fe5vi 0.280 1.483 2.593 0.19 0.17 −0.23 −0.06 −0.22 1.37
  Fe4 0.257 0.955 2.784 0.57 0.13 −0.19 −0.06 −0.24 1.48
  Fe6vii 0.344 2.338 2.399 0.04 0.24 −0.33 −0.08 −0.24 1.33
Fe4 Fe5 0.246 1.038 2.759 0.08 0.21 −0.22 −0.01 −0.05 1.06
  Fe6 0.277 1.211 2.666 0.32 0.22 −0.25 −0.03 −0.12 1.15
Fe5 Fe6viii 0.293 1.777 2.522 0.13 0.22 −0.27 −0.05 −0.15 1.20
Fe6 Fe6ix 0.289 1.653 2.549 0.04 0.22 −0.26 −0.04 −0.15 1.19
Symmetry codes: (i) 1 − x, 1 − y, −z; (ii) 1 + x, y, z; (iii) 1/2 − y, x − 1/2, 1/2 − z; (iv) 1/2 − x, 1/2 + y, 1/2 − z; (v) −x, −y, z; (vi) x − 1/2, 1/2 − y, 1/2 − z; (vii) y − 1/2, 1/2 − x, 1/2 − z; (viii) y, x, z; (ix) 1/2 − y, 1/2 + x, 1/2 − z.

Polarization of the outermost Nd core was observed as a necessity to refine a separate κ and dipole for the 4d105s25p6 shell. This may signify some involvement of these diffuse orbitals in the bonding, as previously observed for Th (Iversen et al., 1998View full citation). One Nd—Nd bond with a distance of 3.57 Å is observed between two symmetry-related Nd1 atoms [Fig. 5[link](d)]. Regardless of the apparent high coordination number of the Nd atoms, only two Nd—Fe bonds are confirmed by BCPs, the Nd1—Fe4 and Nd2—Fe1 with bond lengths of 3.14 Å and 3.20 Å, respectively. Deformation density maps [Figs. 6[link](a) and 6[link](b)] are calculated by subtracting the IAM density from the MM density and show how the MM shifts the density from red regions to blue regions compared with the IAM. B1 clearly has a lone pair (blue contours in Fig. 6[link]) towards Nd1 consistent with a BCP observed between the two atoms with a bond length of 2.90 Å [Figs. 5[link](c), 5[link](d) and 6[link](a)]. The B1—Fe1 and B1—Fe5 bonds have the shortest bond distances of approximately 2.1 Å with the highest electron density in the BCPs. Both Nd1 and Nd2 seem to deform along the c direction, relocating density from within the z = 0 plane to above and below. The effect is most pronounced for Nd1 in Fig. 6[link](b), where pronounced peaks (blue contours, not enclosing the atom centre) of density are seen shifted towards the centre of the cell, slightly above and below z = 0. The same holds true for most of the Fe atoms [Fig. 6[link](b)].

[Figure 6]
Figure 6
Deformation density (ρMMρIAM) and the negative of the Laplacian (−∇2ρb) in the (a) and (c) (001) plane, and (b) and (d) (110) plane. Contours are shown with 0.1 e Å−3 or exponential increments for the deformation density and Laplacian, respectively, positive is blue, negative is red.
3.3.1. Analysis of topological features

Herbst et al. (1985View full citation) hypothesized that the magnetic moment direction along the c axis (easy axis) originates from the anisotropic Fe sublattice. They identify that in general a given Fe atom is coordinated to more Fe neighbours above than below the ab plane in which the Fe atom is placed. The opposite arrangement (with more neighbours below than above) is also found within the unit cell, due to the space-group symmetry (a mirror plane in z = 0.5), but the argument with locally anisotropic structural features in the c direction still holds true.

Fe1 should have 11 contacts in total, 9 Fe: 1 below, 4 in plane and 4 above. The four interactions with Fe3 and Fe4 with distances of 2.52 Å and 2.79 Å, respectively, above the plane were confirmed by the presence of BCPs [Fig. 5[link](f)]. No BCPs were found between Fe1 and Fe5 in the plane, and little to no deformation is observed for either atom in the direction of the interaction. A ring critical point (3, +1) was found in (0, 0, 0) between Fe1 and the symmetry-related Fe1 below, which makes sense since it is a high-symmetry point enclosed by Fe1, B1 and Nd2, but no BCP was found to confirm the Fe1—Fe1 bond. Regardless, some asymmetry is still confirmed in the deformation density map [Fig. 6[link](b)] where the density on Fe1 in the (110) plane is seen to form some mushroom shape in the c direction. In general, the clearest electron deformation relative to the IAM is observed for the Nd and B atoms, Fig. 6[link].

Topological analysis of the coordination environment around Fe2 shows the expected BCPs to Fe5 (2.60 Å) and Fe6 (2.50 Å) symmetrically above and below the plane, in total eight bonds [Fig. 5[link](g)]. Fe3 coordinates to nine Fe atoms (Fe1, Fe3, Fe4, Fe5 and Fe6) in and below the plane with distances between 2.40 Å and 2.78 Å [Fig. 5[link](h)]. Fe4 coordinates to six Fe above and six Fe below [Fig. 5[link](i)]. All 12 Fe4—Fe interactions have distances between 2.64 Å and 2.79 Å with BCPs confirming the structural predictions by Herbst et al. (1985View full citation). Within each of the rings the expected bonds are found. According to Herbst et al. (1985View full citation) Fe5 should coordinate to 11 atoms in total, and 9 Fe: 1 below, 2 in plane and 6 above [Fig. 5[link](j)]. All out-of-plane interactions (2.52–2.76 Å) were confirmed by BCPs, only the in-plane interactions with Fe1 and Fe5 interactions are missing. This aligns with what was observed for Fe1 and confirms the local asymmetry in Fe coordination. All 10 expected Fe interactions (Fe2, Fe4, Fe5 and Fe6) with Fe6 are confirmed by BCPs (2.40–2.67 Å) expressing local anisotropy [Fig. 5[link](k)].

Herbst et al. (1985View full citation) and Shoemaker et al. (1984View full citation) differ in only two aspects: (1) Herbst et al. (1985View full citation) did not consider a bond between Nd1 and Nd2 while Shoemaker et al. (1984View full citation) did, and (2) Herbst et al. (1985View full citation) reported that the Fe1—Fe1 distance is shorter than the Fe1—Fe4 separation and that there is a bond. We agree with Herbst et al. (1985View full citation) that there is no bond between Nd1 and Nd2, but find an Nd1—Nd1 BCP. For the Fe1 interactions, we find that the Fe1—Fe4 distance [2.77275 (5) Å] is shorter than the Fe1—Fe1 distance [2.81971 (7) Å], in agreement with Shoemaker et al. (1984View full citation). This is further supported by a BCP between Fe1 and Fe4, where none is present between Fe1 and Fe1.

3.3.2. Classification of bonds

Based on the dichotomous classification depending on the sign of ∇2ρb, all interactions are closed-shell (∇2ρb > 0, |λ1,2|/λ3 ≪ 1, ρb ≃ 0.1–0.5 e Å−3) ionic or van der Waals (vdW) interactions (Gatti, 2005View full citation). Interactions between B and Fe have higher ρb ≃ 0.5 e Å−3 and ∇2ρb ≃ 3.5 e Å−5, approaching values for metal–ligand interactions in transition metal complexes (Grønbech et al., 2023View full citation, Macchi et al., 1998View full citation), while the other interactions have lower values: Nd1—Nd1 0.095 e Å−3 (0.468 e Å−5), Nd—Fe ≃ 0.15 e Å−3 (0.8–1.0 e Å−5) and Fe—Fe 0.23–0.34 e Å−3 (1.0–2.3 e Å−5). Fe—Fe bonds have values consistent with other reports of transition metal–transition metal bonds in metal complexes (Macchi et al., 1998View full citation). The bond distances are correspondingly short for B—Fe (2.10 Å), slightly longer for Fe—Fe (≃2.5–2.8 Å) and longest for interactions with Nd (>3.0 Å).

Kinetic (Gb), potential (Vb) and total (Hb) energy densities can be estimated from the density (ρb) and Laplacian (∇2ρb) values at the BCP according to the Abramov (1997View full citation) approximation,

Mathematical equation

and the local virial theorem (Bader, 1994View full citation),

Mathematical equation

while the total energy is simply a sum of the kinetic and potential energies. Using the energy densities at the BCPs, the bonding analysis can be expanded to the classification by Espinosa et al. (2002View full citation) based on the |Vb|/Gb ratio. In this classification, all interactions in Nd2Fe14B are placed in the transit region between shared-shell and closed-shell interactions with 1 < |Vb |/Gb < 2, Hb < 0 and ∇2ρb > 0. All observed interactions have |Vb |/Gb ≃ 1.1–1.5 and Hb < 0.1 e Å−3 (except Fe—B interactions with Hb ≃ 0.15 e Å−3), well in line with the nature of other metal–metal bonds in crystals. The bond degree (Hb/ρb) approaches zero at the boundary with the closed-shell region, suggesting a more closed-shell nature of the Nd bonds (|Hb/ρb| ≃ 0.05) than the Fe—Fe (|Hb/ρb| ≃ 0.1–0.25) and Fe—B with |Hb/ρb| > 0.3, suggesting a bond degree of 1/3 of a single bond. Classification of bonds based on the properties in the BCPs aligns well with the observed Laplacian maps in Figs. 6[link](c) and 6[link](d).

3.3.3. Atomic charge and d-orbital populations

Charge transfer between atoms is allowed in the MM and integration of the atomic basin gives the Bader charge and other associated atomic properties. It is found that both Nd atoms are positive, +0.91 and +1.05 for Nd1 and Nd2, respectively, and B is negative, −1.7. Fe1, Fe2, Fe3, Fe5 and Fe6 are predominantly neutral, approximately ±0.1, with Fe1 almost exactly neutral (+0.04), while Fe4 is negative −0.44. Empirically, lanthanides have the +III oxidation state, while B is preferably negatively charged, although maximally −III. Fe is typically positively charged with a range of possible oxidation states. Obeying the preferred formal charges of Nd and B would leave the 14 Fe atoms with a formal charge of −0.2. Other rationalizations could be (1) Fe atoms of different charges; and/or (2) neutral Fe atoms accompanied by a reduced charge of Nd, as observed in this study. The calculated Bader charges show larger absolute values for Nd and B compared with Fe, meaning that the primary charge transfer in this compound comes from donation of electrons from Nd to B. Debye temperatures, d-orbital populations, Bader charges, atomic dipole moments and atomic volumes for the Fe atoms can be seen in Table 4[link].

Table 4
d-orbital populations for the Fe atoms derived from the multipole populations

Percentage occupancy is given in parenthesis. The local coordinate system for each Fe atom is placed with the z axis parallel to c and the y axis parallel to (110), except for the Fe4 coordination environment, which is tilted by ∼16° from the c axis to match the linear axis between the centre of the two Fe hexagons above and below. Integrated properties of the atomic basin are reported without uncertainties, but the integrated absolute Lagrangian, L (which should ideally be below 10−4 a.u.) is on the order of 10−3–10−5 a.u. (Volkov et al., 2016View full citation).

  Fe1 Fe2 Fe3 Fe4 Fe5 Fe6
z2 1.25 (21.0) 1.22 (20.4) 1.17 (19.8) 1.26 (20.1) 1.18 (20.4) 1.18 (20.1)
xz 1.15 (19.3) 1.24 (20.8) 1.26 (21.4) 1.37 (21.8) 1.18 (20.4) 1.21 (20.7)
yz 1.23 (20.6) 1.22 (20.4) 1.26 (21.4) 1.27 (20.3) 1.23 (21.2) 1.23 (21.0)
x2y2 1.16 (19.4) 1.11 (18.6) 1.09 (18.4) 1.16 (18.5) 1.06 (18.3) 1.12 (19.1)
xy 1.18 (19.7) 1.18 (19.8) 1.12 (19.0) 1.21 (19.3) 1.14 (19.7) 1.12 (19.1)
Total dpop 5.97 5.97 5.90 6.27 5.79 5.86
Asphericity, α 0.46 0.59 1.50 1.22 0.95 0.62
Bader (e) +0.04 −0.09 −0.09 −0.44 +0.17 +0.11
Lagrangian, L (10−3 a.u.) 3.1 7.9 0.035 3.2 0.64 2.3
Dipole moment (10−30 C m) 1.45 1.02 4.40 0.28 1.34 1.56
Atomic volume (Å3) 11.81 14.95 14.71 14.25 12.45 13.04
Beq at 25 K (Å2) 0.1634 (8) 0.1745 (8) 0.1777 (8) 0.1729 (8) 0.1729 (8) 0.1666 (8)
Debye temperature (K) 396 (3) 371 (2) 365 (2) 361 (2) 372 (2) 385 (2)
Coordination number 4 Fe, 2 B, 2 Nd 8 Fe 9 Fe 12 Fe, 1 Nd 7 Fe, 1 B 10 Fe
μ at 77 K 1.1 2.2 2.7 3.5 2.4 2.4
†Reported by Herbst et al. (1985View full citation).

The d-orbital populations are approximately six electrons for all Fe atoms and are quite spherically distributed. A fully spherical d-orbital splitting would arise from a 20% occupancy of each d orbital. The asphericity, α, is calculated as the mean square error: Mathematical equation, a sum over the five d orbitals where ni is the percentage occupancy of the ith orbital and Mathematical equation is the mean occupancy assuming spherical distribution (20%). For comparison, the asphericity with six d electrons in high-spin configuration of some common coordination environments is approximately an order of magnitude higher than what we observe here: perfect linear, α = 16.7; perfect octahedral, α = 7.4; and experimental octahedral, α = 4.9 [calculated from the experimental d-orbital occupancies of FeSb2 (Grønbech et al., 2020View full citation)]. Our results vary between 0.46 and 1.50, meaning that almost no d-orbital aphericity is observed.

The theoretical maximal spin-only magnetic moment, μS, can be calculated as Mathematical equation, where n is the number of unpaired electrons. Assuming a high-spin configuration, the maximal μS would be reached for five unpaired electrons; for the d6 configuration, approximately observed for the Fe ions here, the expected maximal spin-only moment would be 4.9 μB. Table 4[link] shows that Fe4 has the highest d-orbital population of 6.27 electrons, which would mean that Fe4 has the lowest magnetic moment, in contradiction to neutron experiments (Herbst et al., 1985View full citation) and theoretical calculations (Gu & Ching, 1987View full citation; Toga et al., 2016View full citation). From the generally much lower experimentally observed magnetic moment (Table 4[link]), compared with the theoretical spin-only moment, we can conclude that either the simple spin-only model or the orbital-splitting model is too crude an approximation to reflect the magnetism in Nd2Fe14B.

The lowest atomic volumes are found for Fe1 and Fe5, both with relatively short bonds to B. Atomic vibrations are very similar for all Fe atoms at 25 K, with the lowest Debye temperature being that of Fe4 [361 (2) K] and highest that of Fe1 [396 (3) K]. Fe4 has a remarkably low electric dipole moment of 0.28 × 10−30 C m, while Fe3 has a moment as high as 4.4 × 10−30 C m, serving as evidence of the very symmetric or asymmetric coordination environment, respectively. No single parameter seems to be a strong descriptor for the varying magnetic moments between the Fe atoms.

3.4. Structure and magnetism

Nd2Fe14B is a metal with resistivity (ρ = 130–150 µΩ cm at room temperature) only slightly higher than many d-block metals (Bovda et al., 2006View full citation; Stankiewicz & Bartolomé, 1999View full citation). The magnetism in Nd2Fe14B can be described as a 4f–3d exchange interaction between the lower lying 4f electrons of Nd and the 3d electrons of Fe close to the Fermi level (Min et al., 1993View full citation). It is generally accepted that the magnetism of rare-earth intermetallic compounds is very complex and that the resulting magnetic ordering arises from contributions from both types of electrons. The magnetic ordering can be viewed as a 4f stabilization of the 3d free electron sea, meaning that the Fe framework forms a metallic magnetic pathway with contributions from the Nd electrons residing in the 4f orbitals.

It is well established that the crystallographic c direction is the easy axis of magnetization, and that the strong magnetic moment originates mainly from the Fe sublattice (Herbst, 1991View full citation; Hirosawa et al., 1986View full citation; Sagawa et al., 1985View full citation; Givord et al., 1984View full citation; Sinnema et al., 1984View full citation). Fe4 possess the strongest magnetic moment (2.7–3.5 µB) of all Fe atoms with the rest being only slightly smaller on average, ∼2.2 µB (Tharp et al., 1987View full citation; Toga et al., 2016View full citation). The local anisotropic coordination along the c direction for all Fe atoms is assumed to improve the magnetic interactions (Herbst et al., 1985View full citation). The strong preference for magnetic stability along the c direction was reported to arise from Nd, with a magnetic moment (3.27 µB) close to that of a free Nd3+ ion (Sagawa et al., 1985View full citation; Givord et al., 1984View full citation), specifically Nd1 was found to stabilize and dictate the magnetic easy axis (Haskel et al., 2005View full citation). Several reports note that Nd and Fe4 must have a favourable strong interaction due to the much higher magnetic moment of Fe4 in Nd2Fe14B than in Y2Fe14B (Gu & Ching, 1987View full citation; Wolfers et al., 2001View full citation). This fits well with the BCP observed here between Nd1 and Fe4. Fe atoms surrounded by B should have a lower 3d magnetic moment due to an ineffective 2p–3d charge transfer/hybridization, which explains the low magnetic moment of Fe1 (Givord et al., 1985View full citation).

The molecular graph of Nd2Fe14B in Fig. 7[link] (showing only Fe—Fe bonds with BCPs) reveals a comprehensive framework of interactions. Each Nd contributes with only one bond to the Fe framework: Nd2—Fe1, where the interaction lies almost in the ab plane, and Nd1—Fe4, which lies along the c direction. Except for the interactions with Nd, Fe2 stands out as the crucial link to facilitate a pathway along the c direction. Without this link, the interaction would be solely two-dimensional within the Fe sandwich layers. None of the Fe atoms in the Fe sandwich layers (Fe1, Fe3, Fe4, Fe5 or Fe6) serve as crucial a role as Fe2. Removing either one of the Fe atoms will not reduce the dimensionality of the framework further, and while Fe4 still stands out as the atom with most interactions and a negative charge, even the link between the triangular-hexagonal layers is maintained without Fe4. The bonds determined by topological analysis of the electron density agree with the relative strength of magnetic interactions between different crystallographic sites as reported by Bouaziz et al. (2023View full citation). Relatively few electron density studies have been performed on metallic solids (Iversen et al., 1995View full citation; Bader, 1994View full citation). These usually crystallize in highly symmetric space groups with few degrees of freedom, which also restricts the topological fingerprint. Nd2Fe14B crystallizes in the tetragonal crystal system. The unusually high number of independent atoms in the asymmetric unit (two Nd, six Fe and B) provides abundant degrees of freedom to describe the comprehensive topology of the metal.

[Figure 7]
Figure 7
Molecular graph showing only the Fe–Fe interactions with grey lines indicating bonds with BCPs. The 25 K structure is used for visualization with thermal ellipsoids shown at a 99% probability level.

4. Conclusions

Multi-temperature synchrotron SCXRD data have been measured on the super-strong permanent magnet Nd2Fe14B. Despite a very low X-ray electron density suitability factor, it was possible to obtain a multipole electron density model at 25 K. A linear, though minute, expansion of the unit cell is observed in the c direction [6.6 (7) × 10−6 K−1], while the ab plane remains unchanged in the investigated temperature range from 25 K to 300 K. In general, very few Nd2Fe14B structures are reported with vibrational parameters, and those attempting a refinement significantly overestimate the vibrations of B. Here we report vibrational parameters of Beq ≃ 0.5 Å2 for Nd and Fe, and Beq = 0.658 (7) for B at 300 K. The material's Debye temperature was estimated from vibrational parameters to be 345–383 K, which is lower than the 418 (12) K reported from heat capacity measurements.

A multipole electron density was derived in line with the Hansen–Coppens multipolar formalism with lmax = 4. Satisfactory modelling of the Nd atoms required a dipole deformation of the core. Deformation densities and QTAIM analysis of the topological features of the electron density show local anisotropy in the bonding environment of the Fe atoms, confirming bonding information suggested by Herbst et al. (1985View full citation) based on atom proximity. By Bader topological analysis it was found that Nd atoms are positive (∼+1), B and Fe4 are negative (−1.7 and −0.44, respectively) and the remaining Fe atoms are neutral (±0.1). The d orbitals of Fe are close to evenly populated. The molecular graph showing a comprehensive framework of Fe interactions, with very little influence from the Nd atoms, serves as a visual chemical descriptor of the 4f–3d exchange magnetic ordering interaction in Nd2Fe14B and highlights the crucial role of Fe2 on the 3D properties of the framework.

Supporting information


Computing details top

(nd2fe14b_100k) top
Crystal data top
BFe14Nd2Dx = 7.582 Mg m3
Mr = 1081.19Synchrotron radiation, λ = 0.2482 Å
Tetragonal, P42/mnmCell parameters from 4161 reflections
a = 8.8135 (2) Åθ = 1.0–18.1°
c = 12.1933 (3) ŵ = 4.31 mm1
V = 947.15 (5) Å3T = 100 K
Z = 4Block, black
F(000) = 19560.13 × 0.06 × 0.03 mm
Data collection top
Kappa goniometer
diffractometer
Rint = 0.043
Absorption correction: multi-scan
SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.0775 before and 0.0590 after correction. The Ratio of minimum to maximum transmission is 0.7638. The λ/2 correction factor is Not present.
θmax = 18.1°, θmin = 1.0°
Tmin = 0.569, Tmax = 0.745h = 2222
143698 measured reflectionsk = 2222
4161 independent reflectionsl = 3030
4104 reflections with I > 2σ(I)
Refinement top
Refinement on F251 parameters
Least-squares matrix: full0 restraints
R[F2 > 2σ(F2)] = 0.009 w = 1/[σ2(Fo2) + (0.0107P)2]
where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.021(Δ/σ)max = 0.004
S = 1.13Δρmax = 0.88 e Å3
4161 reflectionsΔρmin = 2.50 e Å3
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Nd10.35690 (2)0.35690 (2)0.0000000.00273 (1)
Nd20.77011 (2)0.22989 (2)0.0000000.00270 (1)
Fe10.0000000.0000000.11558 (2)0.00261 (1)
Fe20.0000000.5000000.0000000.00285 (1)
Fe30.09806 (2)0.09806 (2)0.29590 (2)0.00293 (1)
Fe40.31753 (2)0.31753 (2)0.25416 (2)0.00287 (1)
Fe50.56705 (2)0.22492 (2)0.37229 (2)0.00283 (1)
Fe60.13968 (2)0.53685 (2)0.17602 (2)0.00269 (1)
B10.12397 (8)0.12397 (8)0.0000000.00513 (10)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Nd10.00277 (1)0.00277 (1)0.00265 (1)0.00029 (1)0.0000.000
Nd20.00288 (1)0.00288 (1)0.00232 (1)0.00050 (1)0.0000.000
Fe10.00255 (2)0.00255 (2)0.00272 (3)0.00025 (2)0.0000.000
Fe20.00330 (3)0.00278 (3)0.00249 (3)0.00001 (2)0.0000.000
Fe30.00284 (1)0.00284 (1)0.00313 (2)0.00015 (2)0.00013 (1)0.00013 (1)
Fe40.00291 (1)0.00291 (1)0.00279 (2)0.00015 (2)0.00007 (1)0.00007 (1)
Fe50.00286 (1)0.00249 (1)0.00313 (1)0.00008 (1)0.00008 (1)0.00023 (1)
Fe60.00262 (1)0.00267 (1)0.00280 (1)0.00006 (1)0.00013 (1)0.00000 (1)
B10.00576 (16)0.00576 (16)0.0039 (2)0.0004 (2)0.0000.000
Geometric parameters (Å, º) top
Nd1—Fe3i3.2968 (1)Fe1—B1xv2.0913 (7)
Nd1—Fe43.1377 (1)Fe2—Fe5iv2.5891 (1)
Nd1—Fe4ii3.1377 (1)Fe2—Fe5xix2.5891 (1)
Nd1—Fe5iii3.0775 (1)Fe2—Fe5xx2.5891 (1)
Nd1—Fe5iv3.0775 (1)Fe2—Fe5v2.5891 (1)
Nd1—Fe5v3.0775 (1)Fe2—Fe6xxi2.4955 (1)
Nd1—Fe5vi3.0775 (1)Fe2—Fe6xxii2.4955 (1)
Nd1—Fe6vii3.2844 (1)Fe2—Fe62.4955 (1)
Nd1—Fe63.2844 (1)Fe2—Fe6ii2.4955 (1)
Nd1—Fe6ii3.2844 (1)Fe3—Fe3xvi2.4445 (2)
Nd1—Fe6viii3.2844 (1)Fe3—Fe4xvii2.6532 (1)
Nd1—B12.9033 (10)Fe3—Fe42.7825 (1)
Nd2—Fe2ix3.1261 (1)Fe3—Fe4iii2.6532 (1)
Nd2—Fe2viii3.1261 (1)Fe3—Fe5iv2.5913 (1)
Nd2—Fe4x3.0553 (1)Fe3—Fe5iii2.5913 (1)
Nd2—Fe4i3.0553 (1)Fe3—Fe6xviii2.3982 (1)
Nd2—Fe5xi3.0712 (1)Fe3—Fe6xvii2.3982 (1)
Nd2—Fe5xii3.0712 (1)Fe4—Fe52.7526 (1)
Nd2—Fe5i3.0712 (1)Fe4—Fe5iii2.7187 (1)
Nd2—Fe5x3.0712 (1)Fe4—Fe5iv2.7187 (1)
Nd2—Fe6vii3.0766 (1)Fe4—Fe5vii2.7526 (1)
Nd2—Fe6viii3.0766 (1)Fe4—Fe6xviii2.6432 (1)
Nd2—Fe6xiii3.0766 (1)Fe4—Fe62.6648 (1)
Nd2—Fe6xiv3.0766 (1)Fe4—Fe6xvii2.6432 (1)
Fe1—Fe1xv2.8186 (2)Fe4—Fe6vii2.6649 (1)
Fe1—Fe3xvi2.5156 (1)Fe5—Fe5xxiii2.5930 (1)
Fe1—Fe32.5156 (1)Fe5—Fe6vii2.5225 (1)
Fe1—Fe4iii2.7740 (1)Fe5—Fe6xviii2.5326 (1)
Fe1—Fe4xvii2.7740 (1)Fe5—Fe6xii2.4656 (1)
Fe1—Fe5xvii2.4998 (1)Fe5—B1i2.1096 (3)
Fe1—Fe5xviii2.4998 (1)Fe6—Fe6xvii2.5489 (1)
Fe1—Fe5iv2.4998 (1)Fe6—Fe6xxiv2.5489 (1)
Fe1—Fe5iii2.4998 (1)Fe6—Fe6xxii2.5463 (1)
Fe1—B12.0913 (7)
Fe4ii—Nd1—Fe3i146.120 (2)Fe3xvi—Fe3—Nd1xxvii68.239 (2)
Fe4—Nd1—Fe3i48.625 (2)Fe3xvi—Fe3—Nd1xvii68.239 (2)
Fe4ii—Nd1—Fe4162.004 (3)Fe3xvi—Fe3—Nd2xxvii130.752 (2)
Fe4ii—Nd1—Fe6129.374 (1)Fe3xvi—Fe3—Fe160.930 (2)
Fe4ii—Nd1—Fe6vii129.373 (2)Fe3xvi—Fe3—Fe4iii62.569 (2)
Fe4—Nd1—Fe6ii129.373 (1)Fe3xvi—Fe3—Fe4xvii62.569 (2)
Fe4—Nd1—Fe6vii48.967 (2)Fe3xvi—Fe3—Fe4169.461 (2)
Fe4ii—Nd1—Fe6viii48.967 (1)Fe3xvi—Fe3—Fe5iii110.556 (2)
Fe4—Nd1—Fe648.966 (2)Fe3xvi—Fe3—Fe5iv110.556 (2)
Fe4ii—Nd1—Fe6ii48.967 (1)Fe4xvii—Fe3—Nd1xvii62.556 (2)
Fe4—Nd1—Fe6viii129.373 (1)Fe4—Fe3—Nd1xvii120.169 (2)
Fe5vi—Nd1—Fe3i129.270 (2)Fe4iii—Fe3—Nd1xvii117.818 (3)
Fe5iii—Nd1—Fe3i82.476 (2)Fe4—Fe3—Nd1xxvii120.169 (2)
Fe5v—Nd1—Fe3i160.971 (2)Fe4xvii—Fe3—Nd1xxvii117.818 (3)
Fe5iv—Nd1—Fe3i100.453 (3)Fe4iii—Fe3—Nd1xxvii62.556 (2)
Fe5v—Nd1—Fe4112.461 (2)Fe4iii—Fe3—Nd2xxvii118.361 (2)
Fe5iv—Nd1—Fe4ii112.460 (2)Fe4xvii—Fe3—Nd2xxvii118.361 (2)
Fe5iv—Nd1—Fe451.869 (2)Fe4—Fe3—Nd2xxvii59.786 (2)
Fe5iii—Nd1—Fe4ii112.460 (2)Fe4iii—Fe3—Fe4114.257 (2)
Fe5v—Nd1—Fe4ii51.868 (2)Fe4xvii—Fe3—Fe4114.257 (2)
Fe5iii—Nd1—Fe451.869 (2)Fe4iii—Fe3—Fe4xvii118.014 (4)
Fe5vi—Nd1—Fe4ii51.868 (2)Fe5iii—Fe3—Nd1xvii176.671 (3)
Fe5vi—Nd1—Fe4112.461 (2)Fe5iv—Fe3—Nd1xxvii176.671 (3)
Fe5v—Nd1—Fe5vi49.831 (2)Fe5iii—Fe3—Nd1xxvii117.190 (2)
Fe5iv—Nd1—Fe5iii49.831 (2)Fe5iv—Fe3—Nd1xvii117.190 (2)
Fe5vi—Nd1—Fe5iii60.793 (3)Fe5iii—Fe3—Nd2xxvii111.736 (3)
Fe5v—Nd1—Fe5iv60.793 (3)Fe5iv—Fe3—Nd2xxvii111.736 (3)
Fe5v—Nd1—Fe5iii82.357 (3)Fe5iv—Fe3—Fe4iii114.115 (4)
Fe5vi—Nd1—Fe5iv82.357 (3)Fe5iv—Fe3—Fe460.662 (2)
Fe5iii—Nd1—Fe6vii45.462 (2)Fe5iii—Fe3—Fe4xvii114.115 (4)
Fe5iv—Nd1—Fe6vii86.193 (2)Fe5iii—Fe3—Fe4iii63.305 (2)
Fe5iii—Nd1—Fe686.193 (2)Fe5iv—Fe3—Fe4xvii63.305 (2)
Fe5iii—Nd1—Fe6viii87.703 (2)Fe5iii—Fe3—Fe460.662 (2)
Fe5iv—Nd1—Fe645.462 (2)Fe5iv—Fe3—Fe5iii60.044 (3)
Fe5v—Nd1—Fe6vii126.506 (2)Fe6xvii—Fe3—Nd1xxvii122.732 (3)
Fe5iv—Nd1—Fe6viii126.506 (2)Fe6xvii—Fe3—Nd1xvii68.355 (2)
Fe5iii—Nd1—Fe6ii126.506 (2)Fe6xviii—Fe3—Nd1xvii122.732 (3)
Fe5vi—Nd1—Fe6126.506 (2)Fe6xviii—Fe3—Nd1xxvii68.355 (2)
Fe5vi—Nd1—Fe6vii87.703 (2)Fe6xviii—Fe3—Nd2xxvii63.306 (2)
Fe5v—Nd1—Fe6ii45.462 (2)Fe6xvii—Fe3—Nd2xxvii63.306 (2)
Fe5vi—Nd1—Fe6viii45.462 (2)Fe6xviii—Fe3—Fe1112.250 (2)
Fe5iv—Nd1—Fe6ii87.703 (2)Fe6xvii—Fe3—Fe1112.250 (2)
Fe5v—Nd1—Fe687.703 (2)Fe6xvii—Fe3—Fe3xvi121.499 (2)
Fe5vi—Nd1—Fe6ii86.193 (2)Fe6xviii—Fe3—Fe3xvi121.499 (2)
Fe5v—Nd1—Fe6viii86.193 (2)Fe6xviii—Fe3—Fe460.820 (2)
Fe6viii—Nd1—Fe3i104.605 (2)Fe6xviii—Fe3—Fe4xvii173.795 (4)
Fe6vii—Nd1—Fe3i42.741 (2)Fe6xviii—Fe3—Fe4iii63.445 (2)
Fe6ii—Nd1—Fe3i144.191 (2)Fe6xvii—Fe3—Fe460.820 (2)
Fe6—Nd1—Fe3i79.885 (2)Fe6xvii—Fe3—Fe4iii173.795 (4)
Fe6viii—Nd1—Fe6ii97.813 (3)Fe6xvii—Fe3—Fe4xvii63.445 (2)
Fe6viii—Nd1—Fe6vii81.608 (3)Fe6xvii—Fe3—Fe5iv60.590 (2)
Fe6ii—Nd1—Fe6vii171.888 (2)Fe6xviii—Fe3—Fe5iv110.495 (3)
Fe6viii—Nd1—Fe6171.888 (2)Fe6xvii—Fe3—Fe5iii110.495 (3)
Fe6ii—Nd1—Fe681.608 (2)Fe6xviii—Fe3—Fe5iii60.590 (2)
Fe6vii—Nd1—Fe697.812 (3)Fe6xviii—Fe3—Fe6xvii114.410 (4)
B1—Nd1—Fe3i122.753 (1)Fe1i—Fe4—Fe3134.533 (4)
B1—Nd1—Fe4ii81.002 (2)Fe3xxiv—Fe4—Fe1i55.175 (3)
B1—Nd1—Fe481.003 (2)Fe3i—Fe4—Fe1i55.175 (3)
B1—Nd1—Fe5v41.178 (2)Fe3xxiv—Fe4—Fe3152.233 (2)
B1—Nd1—Fe5iii41.178 (2)Fe3xxiv—Fe4—Fe3i54.862 (4)
B1—Nd1—Fe5iv41.178 (2)Fe3i—Fe4—Fe3152.233 (2)
B1—Nd1—Fe5vi41.178 (2)Fe3xxiv—Fe4—Fe5iv103.029 (3)
B1—Nd1—Fe685.944 (1)Fe3i—Fe4—Fe5iv131.669 (4)
B1—Nd1—Fe6vii85.944 (1)Fe3i—Fe4—Fe557.251 (3)
B1—Nd1—Fe6ii85.944 (1)Fe3xxiv—Fe4—Fe5iii131.669 (4)
B1—Nd1—Fe6viii85.944 (1)Fe3xxiv—Fe4—Fe5vii57.251 (3)
Fe2ix—Nd2—Fe2viii170.801 (2)Fe3i—Fe4—Fe5iii103.029 (3)
Fe4i—Nd2—Fe2viii90.9Fe3i—Fe4—Fe5vii99.946 (3)
Fe4i—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe599.946 (3)
Fe4x—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe6vii105.219 (3)
Fe4x—Nd2—Fe2viii90.9Fe3xxiv—Fe4—Fe653.609 (2)
Fe4x—Nd2—Fe4i157.694 (4)Fe3i—Fe4—Fe6vii53.609 (2)
Fe4x—Nd2—Fe5xii113.493 (2)Fe3i—Fe4—Fe6105.219 (3)
Fe4i—Nd2—Fe5i53.397 (2)Fe5vii—Fe4—Fe1i53.783 (2)
Fe4i—Nd2—Fe5xi113.493 (2)Fe5—Fe4—Fe1i53.783 (2)
Fe4i—Nd2—Fe5xii53.397 (2)Fe5iii—Fe4—Fe1i151.077 (2)
Fe4x—Nd2—Fe5i113.493 (2)Fe5iv—Fe4—Fe1i151.077 (2)
Fe4x—Nd2—Fe5xi53.397 (2)Fe5vii—Fe4—Fe3104.687 (3)
Fe4i—Nd2—Fe5x113.493 (2)Fe5iv—Fe4—Fe356.190 (3)
Fe4x—Nd2—Fe5x53.397 (2)Fe5iii—Fe4—Fe356.190 (3)
Fe4i—Nd2—Fe6vii51.069 (2)Fe5—Fe4—Fe3104.687 (3)
Fe4x—Nd2—Fe6xiii137.773 (2)Fe5iv—Fe4—Fe5154.784 (3)
Fe4x—Nd2—Fe6vii137.773 (1)Fe5vii—Fe4—Fe5101.536 (4)
Fe4x—Nd2—Fe6xiv51.069 (2)Fe5iii—Fe4—Fe599.551 (3)
Fe4x—Nd2—Fe6viii51.069 (2)Fe5iv—Fe4—Fe5iii56.964 (3)
Fe4i—Nd2—Fe6xiv137.773 (1)Fe5iii—Fe4—Fe5vii154.784 (2)
Fe4i—Nd2—Fe6viii137.773 (2)Fe5iv—Fe4—Fe5vii99.552 (3)
Fe4i—Nd2—Fe6xiii51.069 (2)Fe6xviii—Fe4—Fe1i105.989 (3)
Fe5xi—Nd2—Fe2viii137.136 (1)Fe6—Fe4—Fe1i97.193 (3)
Fe5i—Nd2—Fe2ix137.136 (1)Fe6xvii—Fe4—Fe1i105.989 (3)
Fe5xii—Nd2—Fe2viii137.136 (1)Fe6vii—Fe4—Fe1i97.194 (3)
Fe5x—Nd2—Fe2ix137.136 (1)Fe6xvii—Fe4—Fe3i154.993 (3)
Fe5x—Nd2—Fe2viii49.380 (1)Fe6xvii—Fe4—Fe352.387 (2)
Fe5xii—Nd2—Fe2ix49.380 (1)Fe6vii—Fe4—Fe399.249 (2)
Fe5xi—Nd2—Fe2ix49.380 (1)Fe6xvii—Fe4—Fe3xxiv101.745 (2)
Fe5i—Nd2—Fe2viii49.380 (1)Fe6—Fe4—Fe399.249 (2)
Fe5xii—Nd2—Fe5xi60.932 (3)Fe6xviii—Fe4—Fe3i101.745 (2)
Fe5xi—Nd2—Fe5i118.562 (3)Fe6xviii—Fe4—Fe352.387 (2)
Fe5x—Nd2—Fe5xi87.934 (2)Fe6xviii—Fe4—Fe3xxiv154.993 (3)
Fe5x—Nd2—Fe5xii118.562 (3)Fe6xviii—Fe4—Fe555.941 (2)
Fe5xii—Nd2—Fe5i87.934 (2)Fe6xvii—Fe4—Fe5iv56.104 (2)
Fe5x—Nd2—Fe5i60.932 (3)Fe6—Fe4—Fe5vii55.471 (2)
Fe5xi—Nd2—Fe6vii163.067 (2)Fe6—Fe4—Fe5iv54.506 (2)
Fe5xii—Nd2—Fe6xiii48.655 (2)Fe6xviii—Fe4—Fe5iv99.772 (3)
Fe5i—Nd2—Fe6xiii104.432 (2)Fe6—Fe4—Fe5iii107.774 (3)
Fe5i—Nd2—Fe6vii48.655 (2)Fe6vii—Fe4—Fe5vii150.707 (4)
Fe5xi—Nd2—Fe6xiii92.684 (2)Fe6xviii—Fe4—Fe5iii56.104 (2)
Fe5i—Nd2—Fe6viii92.684 (2)Fe6—Fe4—Fe5150.707 (4)
Fe5x—Nd2—Fe6xiii163.067 (2)Fe6xvii—Fe4—Fe5iii99.772 (3)
Fe5xii—Nd2—Fe6vii104.432 (2)Fe6vii—Fe4—Fe5iii54.505 (2)
Fe5x—Nd2—Fe6xiv104.432 (2)Fe6xvii—Fe4—Fe5vii55.941 (2)
Fe5i—Nd2—Fe6xiv163.067 (2)Fe6xvii—Fe4—Fe5128.425 (4)
Fe5x—Nd2—Fe6vii92.684 (2)Fe6xviii—Fe4—Fe5vii128.424 (4)
Fe5x—Nd2—Fe6viii48.655 (2)Fe6vii—Fe4—Fe5iv107.774 (3)
Fe5xi—Nd2—Fe6viii104.432 (2)Fe6vii—Fe4—Fe555.471 (2)
Fe5xii—Nd2—Fe6xiv92.684 (2)Fe6xviii—Fe4—Fe6151.397 (4)
Fe5xi—Nd2—Fe6xiv48.655 (2)Fe6—Fe4—Fe6vii136.510 (4)
Fe5xii—Nd2—Fe6viii163.067 (2)Fe6xviii—Fe4—Fe6xvii99.402 (4)
Fe6xiii—Nd2—Fe2ix47.438 (2)Fe6xviii—Fe4—Fe6vii57.394 (3)
Fe6vii—Nd2—Fe2viii47.438 (1)Fe6xvii—Fe4—Fe6vii151.397 (4)
Fe6viii—Nd2—Fe2ix129.043 (2)Fe6xvii—Fe4—Fe657.393 (3)
Fe6vii—Nd2—Fe2ix129.043 (2)Nd2xxvii—Fe5—Nd1i118.763 (3)
Fe6xiv—Nd2—Fe2viii129.043 (2)Fe1i—Fe5—Nd1i113.175 (3)
Fe6xiv—Nd2—Fe2ix47.438 (1)Fe1i—Fe5—Nd2xxvii69.071 (2)
Fe6xiii—Nd2—Fe2viii129.043 (2)Fe1i—Fe5—Fe2xviii130.769 (3)
Fe6viii—Nd2—Fe2viii47.438 (2)Fe1i—Fe5—Fe3i59.191 (3)
Fe6viii—Nd2—Fe6xiv81.878 (3)Fe1i—Fe5—Fe463.546 (3)
Fe6xiii—Nd2—Fe6xiv88.472 (3)Fe1i—Fe5—Fe4i111.037 (3)
Fe6xiii—Nd2—Fe6vii81.878 (3)Fe1i—Fe5—Fe5xxiii58.758 (1)
Fe6vii—Nd2—Fe6xiv146.311 (3)Fe1i—Fe5—Fe6xviii118.586 (3)
Fe6viii—Nd2—Fe6xiii146.311 (3)Fe1i—Fe5—Fe6vii108.667 (3)
Fe6viii—Nd2—Fe6vii88.472 (3)Fe2xviii—Fe5—Nd1i72.886 (2)
Fe1xv—Fe1—Nd2xxv63.810 (2)Fe2xviii—Fe5—Nd2xxvii66.414 (2)
Fe3—Fe1—Nd2xxv112.691 (2)Fe2xviii—Fe5—Fe3i163.955 (3)
Fe3xvi—Fe1—Nd2xxv112.691 (2)Fe2xviii—Fe5—Fe4i114.903 (3)
Fe3xvi—Fe1—Fe1xv150.930 (3)Fe2xviii—Fe5—Fe4111.064 (3)
Fe3—Fe1—Fe1xv150.931 (2)Fe2xviii—Fe5—Fe5xxiii134.649 (1)
Fe3xvi—Fe1—Fe358.139 (5)Fe3i—Fe5—Nd1i116.999 (3)
Fe3xvi—Fe1—Fe4xvii59.972 (3)Fe3i—Fe5—Nd2xxvii114.398 (3)
Fe3—Fe1—Fe4xvii59.972 (3)Fe3i—Fe5—Fe4i63.149 (3)
Fe3xvi—Fe1—Fe4iii59.972 (3)Fe3i—Fe5—Fe459.443 (3)
Fe3—Fe1—Fe4iii59.972 (3)Fe3i—Fe5—Fe5xxiii59.978 (2)
Fe4iii—Fe1—Nd2xxv61.118 (3)Fe4i—Fe5—Nd1i65.207 (3)
Fe4xvii—Fe1—Nd2xxv171.262 (4)Fe4—Fe5—Nd1i175.891 (3)
Fe4xvii—Fe1—Fe1xv124.928 (3)Fe4—Fe5—Nd2xxvii63.005 (2)
Fe4iii—Fe1—Fe1xv124.928 (3)Fe4i—Fe5—Nd2xxvii175.834 (3)
Fe4iii—Fe1—Fe4xvii110.144 (5)Fe4i—Fe5—Fe4113.127 (3)
Fe5xvii—Fe1—Nd2xxv119.440 (2)Fe5xxiii—Fe5—Nd1i65.085 (1)
Fe5iv—Fe1—Nd2xxv119.440 (2)Fe5xxiii—Fe5—Nd2xxvii120.718 (1)
Fe5iii—Fe1—Nd2xxv63.941 (2)Fe5xxiii—Fe5—Fe4i61.518 (2)
Fe5xviii—Fe1—Nd2xxv63.941 (2)Fe5xxiii—Fe5—Fe4110.808 (2)
Fe5xvii—Fe1—Fe1xv93.391 (3)Fe6xii—Fe5—Nd1i71.707 (2)
Fe5iii—Fe1—Fe1xv93.391 (3)Fe6vii—Fe5—Nd1i119.858 (3)
Fe5iv—Fe1—Fe1xv93.391 (3)Fe6xviii—Fe5—Nd1i124.160 (2)
Fe5xviii—Fe1—Fe1xv93.391 (3)Fe6xii—Fe5—Nd2xxvii117.627 (3)
Fe5iii—Fe1—Fe3xvi111.267 (4)Fe6xviii—Fe5—Nd2xxvii65.783 (2)
Fe5iv—Fe1—Fe362.217 (3)Fe6vii—Fe5—Nd2xxvii115.454 (3)
Fe5xviii—Fe1—Fe3111.267 (4)Fe6xii—Fe5—Fe1i169.418 (4)
Fe5xviii—Fe1—Fe3xvi62.217 (3)Fe6vii—Fe5—Fe2xviii108.572 (3)
Fe5iii—Fe1—Fe362.217 (3)Fe6xviii—Fe5—Fe2xviii58.305 (2)
Fe5xvii—Fe1—Fe3xvi62.217 (3)Fe6xii—Fe5—Fe2xviii59.105 (2)
Fe5xvii—Fe1—Fe3111.267 (4)Fe6xviii—Fe5—Fe3i106.611 (3)
Fe5iv—Fe1—Fe3xvi111.267 (4)Fe6xii—Fe5—Fe3i110.298 (3)
Fe5xvii—Fe1—Fe4xvii62.671 (2)Fe6vii—Fe5—Fe3i55.915 (3)
Fe5xviii—Fe1—Fe4xvii113.039 (3)Fe6xii—Fe5—Fe4i61.636 (2)
Fe5xviii—Fe1—Fe4iii62.671 (2)Fe6vii—Fe5—Fe4i60.435 (2)
Fe5iv—Fe1—Fe4iii113.039 (3)Fe6xviii—Fe5—Fe459.843 (2)
Fe5iv—Fe1—Fe4xvii62.671 (2)Fe6vii—Fe5—Fe460.500 (2)
Fe5iii—Fe1—Fe4xvii113.039 (3)Fe6xviii—Fe5—Fe4i111.235 (3)
Fe5xvii—Fe1—Fe4iii113.039 (3)Fe6xii—Fe5—Fe4111.092 (3)
Fe5iii—Fe1—Fe4iii62.671 (2)Fe6xviii—Fe5—Fe5xxiii166.286 (2)
Fe5iv—Fe1—Fe5iii62.484 (3)Fe6vii—Fe5—Fe5xxiii106.572 (2)
Fe5xviii—Fe1—Fe5xvii62.484 (3)Fe6xii—Fe5—Fe5xxiii118.560 (2)
Fe5iii—Fe1—Fe5xvii173.218 (6)Fe6xii—Fe5—Fe6xviii61.236 (3)
Fe5iv—Fe1—Fe5xviii173.218 (6)Fe6vii—Fe5—Fe6xviii60.560 (2)
Fe5iv—Fe1—Fe5xvii117.065 (3)Fe6xii—Fe5—Fe6vii61.447 (3)
Fe5iii—Fe1—Fe5xviii117.065 (3)B1i—Fe5—Nd1i64.98 (3)
B1xv—Fe1—Nd2xxv72.698 (7)B1i—Fe5—Nd2xxvii75.315 (18)
B1—Fe1—Nd2xxv72.698 (7)B1i—Fe5—Fe1i53.15 (2)
B1—Fe1—Fe1xv47.633 (19)B1i—Fe5—Fe2xviii95.376 (10)
B1xv—Fe1—Fe1xv47.633 (19)B1i—Fe5—Fe3i100.311 (12)
B1xv—Fe1—Fe3xvi103.297 (19)B1i—Fe5—Fe4i108.204 (17)
B1xv—Fe1—Fe3161.436 (19)B1i—Fe5—Fe4112.89 (3)
B1—Fe1—Fe3103.297 (19)B1i—Fe5—Fe5xxiii52.078 (6)
B1—Fe1—Fe3xvi161.437 (19)B1i—Fe5—Fe6xviii139.111 (11)
B1—Fe1—Fe4iii112.695 (9)B1i—Fe5—Fe6xii134.86 (3)
B1—Fe1—Fe4xvii112.695 (9)B1i—Fe5—Fe6vii155.989 (8)
B1xv—Fe1—Fe4xvii112.695 (9)Nd2xiv—Fe6—Nd173.511 (2)
B1xv—Fe1—Fe4iii112.695 (9)Fe2—Fe6—Nd170.286 (2)
B1—Fe1—Fe5iii53.820 (14)Fe2—Fe6—Nd2xiv67.322 (2)
B1xv—Fe1—Fe5iv132.071 (14)Fe2—Fe6—Fe4xxiv117.982 (3)
B1xv—Fe1—Fe5xviii53.820 (14)Fe2—Fe6—Fe4120.218 (3)
B1xv—Fe1—Fe5xvii53.820 (14)Fe2—Fe6—Fe5vii167.597 (3)
B1—Fe1—Fe5iv53.820 (14)Fe2—Fe6—Fe5xix61.981 (2)
B1—Fe1—Fe5xvii132.071 (14)Fe2—Fe6—Fe6xvii110.728 (3)
B1—Fe1—Fe5xviii132.071 (14)Fe2—Fe6—Fe6xxiv110.728 (3)
B1xv—Fe1—Fe5iii132.071 (14)Fe2—Fe6—Fe6xxii59.323 (2)
B1xv—Fe1—B195.27 (4)Fe3xxiv—Fe6—Nd168.905 (3)
Nd1—Fe2—Nd1xxi180.0Fe3xxiv—Fe6—Nd2xiv72.554 (2)
Nd2xxvi—Fe2—Nd1108.552 (1)Fe3xxiv—Fe6—Fe2128.869 (3)
Nd2xxvi—Fe2—Nd1xxi71.448 (1)Fe3xxiv—Fe6—Fe462.946 (3)
Nd2xiv—Fe2—Nd1xxi108.552 (1)Fe3xxiv—Fe6—Fe4xxiv66.792 (3)
Nd2xiv—Fe2—Nd171.448 (1)Fe3xxiv—Fe6—Fe5vii63.495 (3)
Nd2xxvi—Fe2—Nd2xiv180.0Fe3xxiv—Fe6—Fe5iv119.659 (3)
Fe5xx—Fe2—Nd1xxi60.215 (2)Fe3xxiv—Fe6—Fe5xix125.405 (3)
Fe5xix—Fe2—Nd1119.786 (2)Fe3xxiv—Fe6—Fe6xxiv114.034 (4)
Fe5iv—Fe2—Nd1xxi119.785 (2)Fe3xxiv—Fe6—Fe6xvii112.269 (4)
Fe5v—Fe2—Nd160.214 (2)Fe3xxiv—Fe6—Fe6xxii171.631 (3)
Fe5xix—Fe2—Nd1xxi60.215 (2)Fe4—Fe6—Nd162.646 (2)
Fe5iv—Fe2—Nd160.214 (1)Fe4xxiv—Fe6—Nd1125.395 (2)
Fe5v—Fe2—Nd1xxi119.785 (2)Fe4—Fe6—Nd2xiv125.601 (3)
Fe5xx—Fe2—Nd1119.786 (1)Fe4xxiv—Fe6—Nd2xiv64.049 (2)
Fe5v—Fe2—Nd2xxvi64.205 (2)Fe4xxiv—Fe6—Fe4118.670 (2)
Fe5v—Fe2—Nd2xiv115.795 (2)Fe5xix—Fe6—Nd1125.689 (3)
Fe5xx—Fe2—Nd2xiv64.205 (1)Fe5vii—Fe6—Nd1119.823 (3)
Fe5xix—Fe2—Nd2xxvi115.795 (2)Fe5iv—Fe6—Nd162.831 (2)
Fe5xix—Fe2—Nd2xiv64.205 (2)Fe5vii—Fe6—Nd2xiv120.958 (3)
Fe5xx—Fe2—Nd2xxvi115.795 (2)Fe5xix—Fe6—Nd2xiv65.561 (2)
Fe5iv—Fe2—Nd2xxvi64.205 (1)Fe5iv—Fe6—Nd2xiv121.714 (3)
Fe5iv—Fe2—Nd2xiv115.795 (2)Fe5iv—Fe6—Fe262.914 (2)
Fe5v—Fe2—Fe5iv73.944 (3)Fe5xix—Fe6—Fe4168.837 (3)
Fe5v—Fe2—Fe5xx106.056 (3)Fe5iv—Fe6—Fe463.860 (3)
Fe5v—Fe2—Fe5xix180.0Fe5vii—Fe6—Fe464.029 (3)
Fe5xix—Fe2—Fe5iv106.056 (3)Fe5iv—Fe6—Fe4xxiv171.773 (3)
Fe5xx—Fe2—Fe5iv180.0Fe5vii—Fe6—Fe4xxiv63.461 (3)
Fe5xix—Fe2—Fe5xx73.944 (3)Fe5xix—Fe6—Fe4xxiv64.216 (3)
Fe6—Fe2—Nd1xxi114.170 (2)Fe5iv—Fe6—Fe5vii113.749 (3)
Fe6ii—Fe2—Nd1xxi114.170 (2)Fe5iv—Fe6—Fe5xix111.719 (3)
Fe6—Fe2—Nd165.830 (2)Fe5vii—Fe6—Fe5xix111.464 (3)
Fe6ii—Fe2—Nd165.830 (2)Fe5iv—Fe6—Fe6xxiv110.080 (2)
Fe6xxii—Fe2—Nd1xxi65.830 (2)Fe5xix—Fe6—Fe6xxii58.087 (2)
Fe6xxii—Fe2—Nd1114.170 (2)Fe5vii—Fe6—Fe6xxii108.356 (2)
Fe6xxi—Fe2—Nd1114.170 (2)Fe5vii—Fe6—Fe6xxiv58.180 (3)
Fe6xxi—Fe2—Nd1xxi65.830 (2)Fe5vii—Fe6—Fe6xvii59.917 (3)
Fe6xxi—Fe2—Nd2xiv114.761 (2)Fe5xix—Fe6—Fe6xvii107.960 (2)
Fe6xxi—Fe2—Nd2xxvi65.239 (2)Fe5iv—Fe6—Fe6xxii60.678 (3)
Fe6xxii—Fe2—Nd2xxvi65.239 (2)Fe5xix—Fe6—Fe6xxiv59.524 (3)
Fe6ii—Fe2—Nd2xiv65.239 (2)Fe5iv—Fe6—Fe6xvii60.374 (3)
Fe6ii—Fe2—Nd2xxvi114.761 (2)Fe6xxii—Fe6—Nd1116.132 (2)
Fe6xxii—Fe2—Nd2xiv114.761 (2)Fe6xxiv—Fe6—Nd1171.906 (3)
Fe6—Fe2—Nd2xiv65.239 (2)Fe6xvii—Fe6—Nd1112.028 (3)
Fe6—Fe2—Nd2xxvi114.761 (2)Fe6xxii—Fe6—Nd2xiv114.855 (2)
Fe6—Fe2—Fe5xx122.019 (2)Fe6xxiv—Fe6—Nd2xiv114.452 (3)
Fe6ii—Fe2—Fe5xx59.713 (2)Fe6xvii—Fe6—Nd2xiv173.493 (3)
Fe6—Fe2—Fe5v120.287 (2)Fe6xvii—Fe6—Fe460.877 (3)
Fe6xxii—Fe2—Fe5iv59.713 (2)Fe6xvii—Fe6—Fe4xxiv113.206 (3)
Fe6ii—Fe2—Fe5v57.981 (2)Fe6xxii—Fe6—Fe4112.565 (3)
Fe6—Fe2—Fe5iv57.981 (2)Fe6xxiv—Fe6—Fe4xxiv61.730 (3)
Fe6xxii—Fe2—Fe5xix57.981 (2)Fe6xxii—Fe6—Fe4xxiv112.131 (3)
Fe6xxii—Fe2—Fe5xx120.287 (2)Fe6xxiv—Fe6—Fe4111.338 (3)
Fe6xxi—Fe2—Fe5v59.713 (2)Fe6xxii—Fe6—Fe6xxiv60.034 (1)
Fe6xxi—Fe2—Fe5iv122.019 (2)Fe6xvii—Fe6—Fe6xxiv59.933 (3)
Fe6xxii—Fe2—Fe5v122.019 (2)Fe6xxii—Fe6—Fe6xvii60.034 (2)
Fe6ii—Fe2—Fe5xix122.019 (2)Fe1xv—B1—Nd1137.634 (19)
Fe6xxi—Fe2—Fe5xix120.287 (3)Fe1—B1—Nd1137.633 (19)
Fe6ii—Fe2—Fe5iv120.287 (2)Fe1xv—B1—Fe184.73 (4)
Fe6xxi—Fe2—Fe5xx57.981 (2)Fe1—B1—Fe5v134.67 (3)
Fe6—Fe2—Fe5xix59.713 (2)Fe1xv—B1—Fe5v73.032 (10)
Fe6ii—Fe2—Fe6xxii180.0Fe1xv—B1—Fe5iii134.67 (3)
Fe6xxi—Fe2—Fe6xxii118.648 (3)Fe1xv—B1—Fe5iv134.67 (3)
Fe6xxii—Fe2—Fe661.352 (3)Fe1—B1—Fe5vi134.67 (3)
Fe6xxi—Fe2—Fe6180.0Fe1—B1—Fe5iv73.031 (10)
Fe6ii—Fe2—Fe6118.648 (3)Fe1—B1—Fe5iii73.031 (10)
Fe6xxi—Fe2—Fe6ii61.352 (3)Fe1xv—B1—Fe5vi73.032 (10)
Nd1xvii—Fe3—Nd1xxvii65.506 (2)Fe5v—B1—Nd173.85 (3)
Nd2xxvii—Fe3—Nd1xxvii70.741 (2)Fe5iii—B1—Nd173.84 (3)
Nd2xxvii—Fe3—Nd1xvii70.741 (2)Fe5iv—B1—Nd173.84 (3)
Fe1—Fe3—Nd1xvii118.663 (3)Fe5vi—B1—Nd173.85 (3)
Fe1—Fe3—Nd1xxvii118.663 (3)Fe5iv—B1—Fe5iii75.844 (12)
Fe1—Fe3—Nd2xxvii168.317 (3)Fe5v—B1—Fe5vi75.844 (12)
Fe1—Fe3—Fe4xvii64.854 (2)Fe5iii—B1—Fe5vi95.149 (17)
Fe1—Fe3—Fe4iii64.854 (2)Fe5iii—B1—Fe5v147.69 (5)
Fe1—Fe3—Fe4108.531 (4)Fe5iv—B1—Fe5vi147.69 (5)
Fe1—Fe3—Fe5iv58.592 (3)Fe5iv—B1—Fe5v95.149 (17)
Fe1—Fe3—Fe5iii58.592 (3)
Symmetry codes: (i) y+1/2, x+1/2, z+1/2; (ii) x, y, z; (iii) y+1/2, x1/2, z+1/2; (iv) x1/2, y+1/2, z+1/2; (v) x1/2, y+1/2, z1/2; (vi) y+1/2, x1/2, z1/2; (vii) y, x, z; (viii) y, x, z; (ix) x+1, y, z; (x) y+1/2, x+1/2, z1/2; (xi) x+1/2, y+1/2, z1/2; (xii) x+1/2, y+1/2, z+1/2; (xiii) x+1, y+1, z; (xiv) x+1, y+1, z; (xv) x, y, z; (xvi) x, y, z; (xvii) y1/2, x+1/2, z+1/2; (xviii) x+1/2, y1/2, z+1/2; (xix) x+1/2, y+1/2, z+1/2; (xx) x+1/2, y+1/2, z1/2; (xxi) x, y+1, z; (xxii) x, y+1, z; (xxiii) y+1, x+1, z; (xxiv) y+1/2, x+1/2, z+1/2; (xxv) x+1, y, z; (xxvi) x1, y, z; (xxvii) y+1/2, x1/2, z+1/2.
(nd2fe14b_200k) top
Crystal data top
BFe14Nd2Dx = 7.573 Mg m3
Mr = 1081.19Synchrotron radiation, λ = 0.2482 Å
Tetragonal, P42/mnmCell parameters from 4164 reflections
a = 8.81530 (14) Åθ = 1.8–18.1°
c = 12.2028 (2) ŵ = 4.30 mm1
V = 948.27 (3) Å3T = 200 K
Z = 4Block, black
F(000) = 19560.13 × 0.06 × 0.03 mm
Data collection top
Kappa goniometer
diffractometer
Rint = 0.047
Absorption correction: multi-scan
SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.0775 before and 0.0590 after correction. The Ratio of minimum to maximum transmission is 0.7638. The λ/2 correction factor is Not present.
θmax = 18.1°, θmin = 1.8°
Tmin = 0.594, Tmax = 0.801h = 2222
143551 measured reflectionsk = 2222
4164 independent reflectionsl = 3030
4059 reflections with I > 2σ(I)
Refinement top
Refinement on F251 parameters
Least-squares matrix: full0 restraints
R[F2 > 2σ(F2)] = 0.009 w = 1/[σ2(Fo2) + (0.0113P)2]
where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.022(Δ/σ)max = 0.003
S = 1.07Δρmax = 0.75 e Å3
4164 reflectionsΔρmin = 2.31 e Å3
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Nd10.35692 (2)0.35692 (2)0.0000000.00461 (1)
Nd20.77006 (2)0.22994 (2)0.0000000.00451 (1)
Fe10.0000000.0000000.11531 (2)0.00391 (1)
Fe20.0000000.5000000.0000000.00438 (1)
Fe30.09805 (2)0.09805 (2)0.29561 (2)0.00453 (1)
Fe40.31749 (2)0.31749 (2)0.25420 (2)0.00454 (1)
Fe50.56700 (2)0.22479 (2)0.37234 (2)0.00434 (1)
Fe60.13979 (2)0.53689 (2)0.17603 (2)0.00409 (1)
B10.12421 (8)0.12421 (8)0.0000000.00646 (11)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Nd10.00474 (1)0.00474 (1)0.00435 (1)0.00060 (1)0.0000.000
Nd20.00490 (1)0.00490 (1)0.00374 (1)0.00089 (1)0.0000.000
Fe10.00384 (2)0.00384 (2)0.00403 (3)0.00052 (2)0.0000.000
Fe20.00520 (3)0.00434 (3)0.00360 (3)0.00004 (2)0.0000.000
Fe30.00440 (1)0.00440 (1)0.00478 (2)0.00025 (2)0.00020 (1)0.00020 (1)
Fe40.00466 (1)0.00466 (1)0.00431 (2)0.00025 (2)0.00014 (1)0.00014 (1)
Fe50.00444 (2)0.00370 (2)0.00487 (2)0.00014 (1)0.00014 (1)0.00042 (1)
Fe60.00400 (2)0.00409 (2)0.00418 (2)0.00012 (1)0.00022 (1)0.00001 (1)
B10.00748 (17)0.00748 (17)0.0044 (2)0.0011 (2)0.0000.000
Geometric parameters (Å, º) top
Nd1—Fe3i3.3010 (1)Fe1—B12.0923 (8)
Nd1—Fe43.1407 (1)Fe2—Fe5iv2.5889 (1)
Nd1—Fe4ii3.1406 (1)Fe2—Fe5xix2.5889 (1)
Nd1—Fe5iii3.0785 (1)Fe2—Fe5xx2.5889 (1)
Nd1—Fe5iv3.0785 (1)Fe2—Fe5v2.5889 (1)
Nd1—Fe5v3.0785 (1)Fe2—Fe62.4977 (1)
Nd1—Fe5vi3.0785 (1)Fe2—Fe6ii2.4977 (1)
Nd1—Fe6vii3.2855 (1)Fe2—Fe6xxi2.4977 (1)
Nd1—Fe63.2855 (1)Fe2—Fe6xxii2.4977 (1)
Nd1—Fe6viii3.2855 (1)Fe3—Fe3xvi2.4448 (2)
Nd1—Fe6ii3.2855 (1)Fe3—Fe4iii2.6534 (1)
Nd1—B12.9011 (10)Fe3—Fe42.7820 (1)
Nd2—Fe2ix3.1267 (1)Fe3—Fe4xvii2.6534 (1)
Nd2—Fe2viii3.1267 (1)Fe3—Fe5iv2.5912 (1)
Nd2—Fe4x3.0572 (1)Fe3—Fe5iii2.5912 (1)
Nd2—Fe4i3.0572 (1)Fe3—Fe6xviii2.3981 (1)
Nd2—Fe5xi3.0721 (1)Fe3—Fe6xvii2.3981 (1)
Nd2—Fe5x3.0721 (1)Fe4—Fe52.7539 (1)
Nd2—Fe5i3.0721 (1)Fe4—Fe5iii2.7202 (1)
Nd2—Fe5xii3.0721 (1)Fe4—Fe5iv2.7202 (1)
Nd2—Fe6vii3.0774 (1)Fe4—Fe5vii2.7539 (1)
Nd2—Fe6xiii3.0774 (1)Fe4—Fe6xviii2.6429 (1)
Nd2—Fe6viii3.0774 (1)Fe4—Fe6vii2.6654 (1)
Nd2—Fe6xiv3.0774 (1)Fe4—Fe6xvii2.6429 (1)
Fe1—Fe1xv2.8142 (2)Fe4—Fe62.6655 (1)
Fe1—Fe32.5169 (1)Fe5—Fe5xxiii2.5958 (1)
Fe1—Fe3xvi2.5170 (1)Fe5—Fe6vii2.5240 (1)
Fe1—Fe4xvii2.7772 (1)Fe5—Fe6xviii2.5328 (1)
Fe1—Fe4iii2.7772 (1)Fe5—Fe6xii2.4661 (1)
Fe1—Fe5xvii2.5015 (1)Fe5—B1i2.1102 (3)
Fe1—Fe5xviii2.5015 (1)Fe6—Fe6xxiv2.5510 (1)
Fe1—Fe5iv2.5015 (1)Fe6—Fe6xvii2.5511 (1)
Fe1—Fe5iii2.5015 (1)Fe6—Fe6xxi2.5490 (1)
Fe1—B1xv2.0924 (8)
Fe4ii—Nd1—Fe3i146.184 (2)Fe3xvi—Fe3—Nd1xxvii68.266 (2)
Fe4—Nd1—Fe3i48.572 (2)Fe3xvi—Fe3—Nd1xvii68.266 (2)
Fe4ii—Nd1—Fe4161.991 (4)Fe3xvi—Fe3—Nd2xxvii130.689 (2)
Fe4ii—Nd1—Fe6129.397 (1)Fe3xvi—Fe3—Fe160.944 (2)
Fe4ii—Nd1—Fe6vii129.398 (1)Fe3xvi—Fe3—Fe4xvii62.569 (2)
Fe4—Nd1—Fe6viii129.398 (1)Fe3xvi—Fe3—Fe4iii62.569 (2)
Fe4—Nd1—Fe6vii48.946 (1)Fe3xvi—Fe3—Fe4169.534 (3)
Fe4ii—Nd1—Fe6ii48.946 (1)Fe3xvi—Fe3—Fe5iii110.577 (2)
Fe4—Nd1—Fe648.947 (1)Fe3xvi—Fe3—Fe5iv110.577 (2)
Fe4ii—Nd1—Fe6viii48.946 (1)Fe4iii—Fe3—Nd1xvii117.765 (3)
Fe4—Nd1—Fe6ii129.398 (1)Fe4—Fe3—Nd1xvii120.091 (3)
Fe5vi—Nd1—Fe3i129.258 (2)Fe4xvii—Fe3—Nd1xvii62.556 (2)
Fe5iii—Nd1—Fe3i82.424 (2)Fe4—Fe3—Nd1xxvii120.091 (3)
Fe5v—Nd1—Fe3i160.919 (2)Fe4iii—Fe3—Nd1xxvii62.556 (2)
Fe5iv—Nd1—Fe3i100.393 (2)Fe4xvii—Fe3—Nd1xxvii117.765 (3)
Fe5v—Nd1—Fe4112.459 (2)Fe4xvii—Fe3—Nd2xxvii118.296 (2)
Fe5iv—Nd1—Fe4ii112.458 (2)Fe4iii—Fe3—Nd2xxvii118.296 (2)
Fe5iv—Nd1—Fe451.862 (2)Fe4—Fe3—Nd2xxvii59.777 (3)
Fe5iii—Nd1—Fe4ii112.458 (2)Fe4xvii—Fe3—Fe4114.293 (2)
Fe5v—Nd1—Fe4ii51.862 (2)Fe4iii—Fe3—Fe4114.293 (2)
Fe5iii—Nd1—Fe451.862 (2)Fe4xvii—Fe3—Fe4iii118.074 (4)
Fe5vi—Nd1—Fe4ii51.862 (2)Fe5iii—Fe3—Nd1xvii176.776 (3)
Fe5vi—Nd1—Fe4112.459 (2)Fe5iv—Fe3—Nd1xxvii176.776 (3)
Fe5v—Nd1—Fe5vi49.869 (2)Fe5iii—Fe3—Nd1xxvii117.200 (2)
Fe5iv—Nd1—Fe5iii49.869 (2)Fe5iv—Fe3—Nd1xvii117.200 (2)
Fe5vi—Nd1—Fe5iii60.798 (3)Fe5iii—Fe3—Nd2xxvii111.753 (3)
Fe5v—Nd1—Fe5iv60.798 (3)Fe5iv—Fe3—Nd2xxvii111.753 (3)
Fe5v—Nd1—Fe5iii82.391 (3)Fe5iv—Fe3—Fe4xvii63.336 (2)
Fe5vi—Nd1—Fe5iv82.391 (3)Fe5iv—Fe3—Fe460.706 (3)
Fe5iii—Nd1—Fe6vii45.454 (2)Fe5iii—Fe3—Fe4iii63.336 (2)
Fe5iv—Nd1—Fe6vii86.201 (2)Fe5iii—Fe3—Fe4xvii114.220 (4)
Fe5iii—Nd1—Fe686.201 (2)Fe5iv—Fe3—Fe4iii114.220 (4)
Fe5iii—Nd1—Fe6ii126.542 (2)Fe5iii—Fe3—Fe460.706 (3)
Fe5iv—Nd1—Fe645.454 (2)Fe5iv—Fe3—Fe5iii60.116 (3)
Fe5v—Nd1—Fe6vii126.542 (2)Fe6xvii—Fe3—Nd1xxvii122.585 (3)
Fe5iv—Nd1—Fe6ii87.718 (2)Fe6xvii—Fe3—Nd1xvii68.304 (2)
Fe5iii—Nd1—Fe6viii87.718 (2)Fe6xviii—Fe3—Nd1xvii122.585 (3)
Fe5vi—Nd1—Fe6126.542 (2)Fe6xviii—Fe3—Nd1xxvii68.304 (2)
Fe5vi—Nd1—Fe6vii87.718 (2)Fe6xviii—Fe3—Nd2xxvii63.255 (2)
Fe5v—Nd1—Fe6viii86.201 (2)Fe6xvii—Fe3—Nd2xxvii63.255 (2)
Fe5vi—Nd1—Fe6ii86.201 (2)Fe6xviii—Fe3—Fe1112.326 (3)
Fe5iv—Nd1—Fe6viii126.542 (2)Fe6xvii—Fe3—Fe1112.326 (3)
Fe5v—Nd1—Fe687.717 (2)Fe6xvii—Fe3—Fe3xvi121.496 (2)
Fe5vi—Nd1—Fe6viii45.454 (2)Fe6xviii—Fe3—Fe3xvi121.496 (2)
Fe5v—Nd1—Fe6ii45.454 (2)Fe6xviii—Fe3—Fe460.821 (2)
Fe6ii—Nd1—Fe3i144.199 (2)Fe6xviii—Fe3—Fe4iii63.456 (2)
Fe6vii—Nd1—Fe3i42.703 (1)Fe6xviii—Fe3—Fe4xvii173.908 (4)
Fe6viii—Nd1—Fe3i104.660 (2)Fe6xvii—Fe3—Fe460.821 (2)
Fe6—Nd1—Fe3i79.811 (2)Fe6xvii—Fe3—Fe4xvii63.456 (2)
Fe6ii—Nd1—Fe6viii97.768 (2)Fe6xvii—Fe3—Fe4iii173.908 (4)
Fe6ii—Nd1—Fe6vii171.916 (3)Fe6xvii—Fe3—Fe5iv60.632 (2)
Fe6viii—Nd1—Fe6vii81.657 (2)Fe6xviii—Fe3—Fe5iv110.575 (4)
Fe6ii—Nd1—Fe681.656 (3)Fe6xvii—Fe3—Fe5iii110.575 (4)
Fe6viii—Nd1—Fe6171.916 (3)Fe6xviii—Fe3—Fe5iii60.632 (2)
Fe6vii—Nd1—Fe697.769 (3)Fe6xviii—Fe3—Fe6xvii114.360 (4)
B1—Nd1—Fe3i122.708 (1)Fe1i—Fe4—Fe3134.550 (4)
B1—Nd1—Fe4ii80.995 (2)Fe3xxiv—Fe4—Fe1i55.166 (3)
B1—Nd1—Fe480.996 (2)Fe3i—Fe4—Fe1i55.166 (3)
B1—Nd1—Fe5v41.195 (2)Fe3xxiv—Fe4—Fe3152.231 (2)
B1—Nd1—Fe5iii41.195 (2)Fe3xxiv—Fe4—Fe3i54.863 (4)
B1—Nd1—Fe5iv41.195 (2)Fe3i—Fe4—Fe3152.231 (2)
B1—Nd1—Fe5vi41.195 (2)Fe3xxiv—Fe4—Fe5iv103.029 (3)
B1—Nd1—Fe685.958 (1)Fe3i—Fe4—Fe5iv131.686 (4)
B1—Nd1—Fe6vii85.958 (1)Fe3i—Fe4—Fe557.230 (3)
B1—Nd1—Fe6viii85.958 (1)Fe3xxiv—Fe4—Fe5iii131.686 (4)
B1—Nd1—Fe6ii85.958 (1)Fe3xxiv—Fe4—Fe5vii57.230 (3)
Fe2ix—Nd2—Fe2viii170.823 (2)Fe3i—Fe4—Fe5iii103.029 (3)
Fe4i—Nd2—Fe2viii90.9Fe3i—Fe4—Fe5vii99.928 (3)
Fe4i—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe599.929 (3)
Fe4x—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe653.599 (2)
Fe4x—Nd2—Fe2viii90.9Fe3xxiv—Fe4—Fe6vii105.201 (3)
Fe4x—Nd2—Fe4i157.698 (4)Fe3i—Fe4—Fe6105.201 (4)
Fe4x—Nd2—Fe5x53.397 (2)Fe3i—Fe4—Fe6vii53.599 (2)
Fe4i—Nd2—Fe5i53.397 (1)Fe5vii—Fe4—Fe1i53.776 (2)
Fe4i—Nd2—Fe5xi113.501 (2)Fe5—Fe4—Fe1i53.776 (2)
Fe4i—Nd2—Fe5x113.501 (2)Fe5iii—Fe4—Fe1i151.062 (2)
Fe4x—Nd2—Fe5i113.501 (2)Fe5iv—Fe4—Fe1i151.062 (2)
Fe4x—Nd2—Fe5xi53.397 (1)Fe5vii—Fe4—Fe3104.711 (3)
Fe4i—Nd2—Fe5xii53.397 (2)Fe5iv—Fe4—Fe356.177 (3)
Fe4x—Nd2—Fe5xii113.501 (2)Fe5iii—Fe4—Fe356.177 (3)
Fe4i—Nd2—Fe6vii51.038 (2)Fe5—Fe4—Fe3104.710 (3)
Fe4x—Nd2—Fe6viii51.038 (2)Fe5iv—Fe4—Fe5154.805 (3)
Fe4x—Nd2—Fe6vii137.804 (2)Fe5vii—Fe4—Fe5101.535 (4)
Fe4x—Nd2—Fe6xiv51.038 (2)Fe5iii—Fe4—Fe599.539 (3)
Fe4x—Nd2—Fe6xiii137.804 (2)Fe5iv—Fe4—Fe5iii56.996 (3)
Fe4i—Nd2—Fe6xiv137.804 (2)Fe5iii—Fe4—Fe5vii154.805 (3)
Fe4i—Nd2—Fe6xiii51.038 (2)Fe5iv—Fe4—Fe5vii99.539 (2)
Fe4i—Nd2—Fe6viii137.804 (2)Fe6xviii—Fe4—Fe1i105.960 (3)
Fe5xi—Nd2—Fe2viii137.136 (1)Fe6vii—Fe4—Fe1i97.197 (3)
Fe5i—Nd2—Fe2ix137.136 (1)Fe6xvii—Fe4—Fe1i105.960 (3)
Fe5x—Nd2—Fe2viii49.362 (1)Fe6—Fe4—Fe1i97.198 (3)
Fe5xii—Nd2—Fe2ix49.362 (1)Fe6xvii—Fe4—Fe3i154.982 (3)
Fe5xii—Nd2—Fe2viii137.136 (1)Fe6xvii—Fe4—Fe352.395 (2)
Fe5x—Nd2—Fe2ix137.136 (1)Fe6—Fe4—Fe399.260 (2)
Fe5xi—Nd2—Fe2ix49.362 (1)Fe6xvii—Fe4—Fe3xxiv101.747 (2)
Fe5i—Nd2—Fe2viii49.362 (1)Fe6vii—Fe4—Fe399.260 (2)
Fe5x—Nd2—Fe5xi87.951 (2)Fe6xviii—Fe4—Fe3i101.747 (2)
Fe5xi—Nd2—Fe5i118.589 (3)Fe6xviii—Fe4—Fe352.395 (2)
Fe5xii—Nd2—Fe5xi60.940 (3)Fe6xviii—Fe4—Fe3xxiv154.982 (3)
Fe5xii—Nd2—Fe5x118.589 (3)Fe6xviii—Fe4—Fe555.933 (2)
Fe5x—Nd2—Fe5i60.940 (3)Fe6xvii—Fe4—Fe5iv56.126 (2)
Fe5xii—Nd2—Fe5i87.951 (2)Fe6vii—Fe4—Fe5vii150.698 (4)
Fe5xi—Nd2—Fe6vii163.056 (2)Fe6vii—Fe4—Fe5iv107.780 (3)
Fe5x—Nd2—Fe6viii48.644 (2)Fe6xviii—Fe4—Fe5iv99.805 (3)
Fe5i—Nd2—Fe6viii92.703 (2)Fe6vii—Fe4—Fe5iii54.492 (2)
Fe5i—Nd2—Fe6vii48.644 (2)Fe6—Fe4—Fe5vii55.487 (2)
Fe5xi—Nd2—Fe6viii104.400 (2)Fe6xviii—Fe4—Fe5iii56.126 (2)
Fe5i—Nd2—Fe6xiii104.400 (2)Fe6vii—Fe4—Fe555.487 (2)
Fe5xii—Nd2—Fe6viii163.056 (2)Fe6xvii—Fe4—Fe5iii99.805 (3)
Fe5x—Nd2—Fe6vii92.703 (2)Fe6—Fe4—Fe5iii107.779 (3)
Fe5xii—Nd2—Fe6xiv92.703 (2)Fe6xvii—Fe4—Fe5vii55.934 (2)
Fe5i—Nd2—Fe6xiv163.056 (2)Fe6xvii—Fe4—Fe5128.400 (4)
Fe5xii—Nd2—Fe6vii104.400 (2)Fe6xviii—Fe4—Fe5vii128.401 (4)
Fe5xii—Nd2—Fe6xiii48.644 (2)Fe6—Fe4—Fe5iv54.492 (2)
Fe5xi—Nd2—Fe6xiii92.703 (2)Fe6—Fe4—Fe5150.699 (4)
Fe5x—Nd2—Fe6xiv104.400 (2)Fe6xviii—Fe4—Fe6vii57.443 (3)
Fe5xi—Nd2—Fe6xiv48.644 (2)Fe6vii—Fe4—Fe6136.453 (4)
Fe5x—Nd2—Fe6xiii163.056 (2)Fe6xviii—Fe4—Fe6xvii99.377 (4)
Fe6viii—Nd2—Fe2ix129.021 (1)Fe6xviii—Fe4—Fe6151.419 (4)
Fe6vii—Nd2—Fe2viii47.472 (1)Fe6xvii—Fe4—Fe657.443 (3)
Fe6xiii—Nd2—Fe2ix47.472 (1)Fe6xvii—Fe4—Fe6vii151.419 (4)
Fe6vii—Nd2—Fe2ix129.021 (2)Nd2xxvii—Fe5—Nd1i118.762 (2)
Fe6xiv—Nd2—Fe2viii129.021 (2)Fe1i—Fe5—Nd1i113.106 (3)
Fe6xiv—Nd2—Fe2ix47.472 (1)Fe1i—Fe5—Nd2xxvii69.041 (2)
Fe6viii—Nd2—Fe2viii47.472 (1)Fe1i—Fe5—Fe2xviii130.712 (3)
Fe6xiii—Nd2—Fe2viii129.021 (1)Fe1i—Fe5—Fe3i59.206 (3)
Fe6xiii—Nd2—Fe6xiv88.535 (2)Fe1i—Fe5—Fe463.587 (3)
Fe6viii—Nd2—Fe6xiv81.820 (3)Fe1i—Fe5—Fe4i111.022 (3)
Fe6viii—Nd2—Fe6vii88.534 (2)Fe1i—Fe5—Fe5xxiii58.745 (1)
Fe6vii—Nd2—Fe6xiv146.320 (3)Fe1i—Fe5—Fe6xviii118.579 (3)
Fe6xiii—Nd2—Fe6viii146.320 (3)Fe1i—Fe5—Fe6vii108.678 (4)
Fe6xiii—Nd2—Fe6vii81.820 (3)Fe2xviii—Fe5—Nd1i72.892 (2)
Fe1xv—Fe1—Nd2xxv63.855 (2)Fe2xviii—Fe5—Nd2xxvii66.418 (1)
Fe3xvi—Fe1—Nd2xxv112.655 (2)Fe2xviii—Fe5—Fe3i164.020 (3)
Fe3—Fe1—Nd2xxv112.655 (2)Fe2xviii—Fe5—Fe4i114.955 (3)
Fe3—Fe1—Fe1xv150.944 (3)Fe2xviii—Fe5—Fe4111.096 (3)
Fe3xvi—Fe1—Fe1xv150.943 (2)Fe2xviii—Fe5—Fe5xxiii134.633 (1)
Fe3—Fe1—Fe3xvi58.112 (5)Fe3i—Fe5—Nd1i116.970 (3)
Fe3—Fe1—Fe4iii59.919 (3)Fe3i—Fe5—Nd2xxvii114.381 (3)
Fe3xvi—Fe1—Fe4iii59.920 (3)Fe3i—Fe5—Fe4i63.115 (3)
Fe3—Fe1—Fe4xvii59.919 (3)Fe3i—Fe5—Fe459.435 (3)
Fe3xvi—Fe1—Fe4xvii59.920 (3)Fe3i—Fe5—Fe5xxiii59.941 (2)
Fe4xvii—Fe1—Nd2xxv171.159 (4)Fe4i—Fe5—Nd1i65.245 (3)
Fe4iii—Fe1—Nd2xxv61.131 (2)Fe4—Fe5—Nd1i175.851 (3)
Fe4iii—Fe1—Fe1xv124.986 (3)Fe4—Fe5—Nd2xxvii63.024 (2)
Fe4xvii—Fe1—Fe1xv124.986 (3)Fe4i—Fe5—Nd2xxvii175.810 (3)
Fe4xvii—Fe1—Fe4iii110.028 (5)Fe4i—Fe5—Fe4113.069 (3)
Fe5xvii—Fe1—Nd2xxv119.492 (2)Fe5xxiii—Fe5—Nd1i65.065 (1)
Fe5iv—Fe1—Nd2xxv119.492 (2)Fe5xxiii—Fe5—Nd2xxvii120.706 (1)
Fe5iii—Fe1—Nd2xxv63.946 (2)Fe5xxiii—Fe5—Fe4i61.501 (1)
Fe5xviii—Fe1—Nd2xxv63.946 (2)Fe5xxiii—Fe5—Fe4110.788 (2)
Fe5xvii—Fe1—Fe1xv93.454 (3)Fe6xii—Fe5—Nd1i71.714 (2)
Fe5iii—Fe1—Fe1xv93.454 (3)Fe6vii—Fe5—Nd1i119.875 (3)
Fe5iv—Fe1—Fe1xv93.454 (3)Fe6xviii—Fe5—Nd1i124.225 (3)
Fe5xviii—Fe1—Fe1xv93.454 (3)Fe6xii—Fe5—Nd2xxvii117.686 (3)
Fe5iii—Fe1—Fe362.173 (3)Fe6xviii—Fe5—Nd2xxvii65.788 (2)
Fe5iv—Fe1—Fe3xvi111.192 (4)Fe6vii—Fe5—Nd2xxvii115.484 (3)
Fe5xviii—Fe1—Fe3xvi62.172 (3)Fe6xii—Fe5—Fe1i169.442 (4)
Fe5xviii—Fe1—Fe3111.191 (4)Fe6vii—Fe5—Fe2xviii108.657 (3)
Fe5iii—Fe1—Fe3xvi111.192 (4)Fe6xviii—Fe5—Fe2xviii58.364 (2)
Fe5xvii—Fe1—Fe3111.191 (4)Fe6xii—Fe5—Fe2xviii59.164 (2)
Fe5xvii—Fe1—Fe3xvi62.172 (3)Fe6xviii—Fe5—Fe3i106.610 (3)
Fe5iv—Fe1—Fe362.173 (3)Fe6xii—Fe5—Fe3i110.301 (3)
Fe5xvii—Fe1—Fe4iii112.988 (3)Fe6vii—Fe5—Fe3i55.897 (3)
Fe5xviii—Fe1—Fe4iii62.637 (2)Fe6xii—Fe5—Fe4i61.622 (2)
Fe5xviii—Fe1—Fe4xvii112.988 (3)Fe6vii—Fe5—Fe4i60.389 (3)
Fe5iv—Fe1—Fe4xvii62.637 (2)Fe6xviii—Fe5—Fe459.816 (3)
Fe5iv—Fe1—Fe4iii112.988 (3)Fe6vii—Fe5—Fe460.479 (3)
Fe5iii—Fe1—Fe4iii62.637 (2)Fe6xviii—Fe5—Fe4i111.245 (3)
Fe5xvii—Fe1—Fe4xvii62.637 (2)Fe6xii—Fe5—Fe4111.107 (3)
Fe5iii—Fe1—Fe4xvii112.988 (3)Fe6xviii—Fe5—Fe5xxiii166.251 (2)
Fe5iv—Fe1—Fe5iii62.509 (3)Fe6vii—Fe5—Fe5xxiii106.513 (2)
Fe5xviii—Fe1—Fe5xvii62.509 (3)Fe6xii—Fe5—Fe5xxiii118.517 (2)
Fe5iii—Fe1—Fe5xvii173.092 (6)Fe6xii—Fe5—Fe6xviii61.300 (3)
Fe5iv—Fe1—Fe5xviii173.092 (6)Fe6vii—Fe5—Fe6xviii60.593 (3)
Fe5iv—Fe1—Fe5xvii117.023 (3)Fe6xii—Fe5—Fe6vii61.478 (3)
Fe5iii—Fe1—Fe5xviii117.023 (3)B1i—Fe5—Nd1i64.89 (3)
B1—Fe1—Nd2xxv72.763 (7)B1i—Fe5—Nd2xxvii75.368 (18)
B1xv—Fe1—Nd2xxv72.763 (7)B1i—Fe5—Fe1i53.14 (2)
B1xv—Fe1—Fe1xv47.740 (19)B1i—Fe5—Fe2xviii95.345 (10)
B1—Fe1—Fe1xv47.740 (19)B1i—Fe5—Fe3i100.280 (12)
B1—Fe1—Fe3103.204 (19)B1i—Fe5—Fe4i108.146 (17)
B1—Fe1—Fe3xvi161.317 (19)B1i—Fe5—Fe4112.97 (3)
B1xv—Fe1—Fe3xvi103.203 (19)B1i—Fe5—Fe5xxiii52.044 (6)
B1xv—Fe1—Fe3161.315 (19)B1i—Fe5—Fe6xviii139.166 (11)
B1xv—Fe1—Fe4xvii112.681 (9)B1i—Fe5—Fe6xii134.79 (3)
B1xv—Fe1—Fe4iii112.681 (9)B1i—Fe5—Fe6vii155.929 (9)
B1—Fe1—Fe4iii112.681 (9)Nd2xiv—Fe6—Nd173.485 (2)
B1—Fe1—Fe4xvii112.681 (9)Fe2—Fe6—Nd170.262 (2)
B1xv—Fe1—Fe5iii132.193 (14)Fe2—Fe6—Nd2xiv67.300 (2)
B1—Fe1—Fe5iv53.800 (15)Fe2—Fe6—Fe4xxiv117.984 (3)
B1—Fe1—Fe5xviii132.193 (14)Fe2—Fe6—Fe4120.216 (3)
B1—Fe1—Fe5xvii132.193 (14)Fe2—Fe6—Fe5vii167.530 (3)
B1xv—Fe1—Fe5iv132.193 (14)Fe2—Fe6—Fe5xix61.943 (2)
B1xv—Fe1—Fe5xvii53.800 (15)Fe2—Fe6—Fe6xxiv110.713 (3)
B1xv—Fe1—Fe5xviii53.800 (15)Fe2—Fe6—Fe6xvii110.712 (3)
B1—Fe1—Fe5iii53.800 (15)Fe2—Fe6—Fe6xxi59.319 (1)
B1—Fe1—B1xv95.48 (4)Fe3xxiv—Fe6—Nd168.993 (3)
Nd1xxii—Fe2—Nd1180.0Fe3xxiv—Fe6—Nd2xiv72.646 (3)
Nd2xxvi—Fe2—Nd1xxii71.433 (1)Fe3xxiv—Fe6—Fe2128.964 (3)
Nd2xxvi—Fe2—Nd1108.567 (1)Fe3xxiv—Fe6—Fe462.944 (3)
Nd2xiv—Fe2—Nd171.433 (1)Fe3xxiv—Fe6—Fe4xxiv66.783 (3)
Nd2xiv—Fe2—Nd1xxii108.567 (1)Fe3xxiv—Fe6—Fe5vii63.468 (3)
Nd2xxvi—Fe2—Nd2xiv180.0Fe3xxiv—Fe6—Fe5iv119.708 (3)
Fe5xx—Fe2—Nd1119.773 (1)Fe3xxiv—Fe6—Fe5xix125.463 (3)
Fe5xix—Fe2—Nd1xxii60.227 (1)Fe3xxiv—Fe6—Fe6xvii112.196 (4)
Fe5iv—Fe2—Nd160.227 (1)Fe3xxiv—Fe6—Fe6xxiv113.971 (4)
Fe5v—Fe2—Nd1xxii119.773 (1)Fe3xxiv—Fe6—Fe6xxi171.540 (2)
Fe5xix—Fe2—Nd1119.773 (2)Fe4—Fe6—Nd162.691 (2)
Fe5iv—Fe2—Nd1xxii119.773 (1)Fe4xxiv—Fe6—Nd1125.418 (3)
Fe5v—Fe2—Nd160.227 (2)Fe4—Fe6—Nd2xiv125.641 (3)
Fe5xx—Fe2—Nd1xxii60.227 (1)Fe4xxiv—Fe6—Nd2xiv64.085 (3)
Fe5v—Fe2—Nd2xxvi64.221 (1)Fe4xxiv—Fe6—Fe4118.690 (2)
Fe5v—Fe2—Nd2xiv115.779 (1)Fe5xix—Fe6—Nd1125.643 (3)
Fe5xx—Fe2—Nd2xiv64.221 (2)Fe5vii—Fe6—Nd1119.890 (3)
Fe5xix—Fe2—Nd2xxvi115.779 (1)Fe5iv—Fe6—Nd162.833 (2)
Fe5xix—Fe2—Nd2xiv64.221 (1)Fe5vii—Fe6—Nd2xiv121.038 (3)
Fe5xx—Fe2—Nd2xxvi115.779 (2)Fe5xix—Fe6—Nd2xiv65.569 (2)
Fe5iv—Fe2—Nd2xxvi64.221 (2)Fe5iv—Fe6—Nd2xiv121.662 (3)
Fe5iv—Fe2—Nd2xiv115.779 (2)Fe5iv—Fe6—Fe262.869 (2)
Fe5v—Fe2—Fe5iv73.988 (3)Fe5xix—Fe6—Fe4168.790 (3)
Fe5v—Fe2—Fe5xx106.012 (3)Fe5iv—Fe6—Fe463.885 (3)
Fe5v—Fe2—Fe5xix180.0Fe5vii—Fe6—Fe464.033 (3)
Fe5xix—Fe2—Fe5iv106.012 (3)Fe5iv—Fe6—Fe4xxiv171.746 (3)
Fe5xx—Fe2—Fe5iv180.0Fe5vii—Fe6—Fe4xxiv63.483 (3)
Fe5xix—Fe2—Fe5xx73.988 (3)Fe5xix—Fe6—Fe4xxiv64.251 (3)
Fe6xxi—Fe2—Nd1114.174 (2)Fe5iv—Fe6—Fe5vii113.750 (3)
Fe6xxii—Fe2—Nd1114.174 (2)Fe5iv—Fe6—Fe5xix111.635 (3)
Fe6xxi—Fe2—Nd1xxii65.826 (2)Fe5vii—Fe6—Fe5xix111.475 (3)
Fe6xxii—Fe2—Nd1xxii65.826 (2)Fe5iv—Fe6—Fe6xvii60.378 (3)
Fe6ii—Fe2—Nd165.826 (2)Fe5xix—Fe6—Fe6xxi58.061 (3)
Fe6ii—Fe2—Nd1xxii114.174 (2)Fe5vii—Fe6—Fe6xxi108.292 (2)
Fe6—Fe2—Nd1xxii114.173 (2)Fe5vii—Fe6—Fe6xvii59.874 (3)
Fe6—Fe2—Nd165.827 (2)Fe5vii—Fe6—Fe6xxiv58.143 (3)
Fe6—Fe2—Nd2xiv65.229 (2)Fe5xix—Fe6—Fe6xxiv59.533 (2)
Fe6—Fe2—Nd2xxvi114.771 (2)Fe5iv—Fe6—Fe6xxi60.640 (3)
Fe6ii—Fe2—Nd2xxvi114.771 (2)Fe5xix—Fe6—Fe6xvii107.956 (2)
Fe6xxii—Fe2—Nd2xiv114.771 (1)Fe5iv—Fe6—Fe6xxiv110.067 (3)
Fe6xxii—Fe2—Nd2xxvi65.229 (1)Fe6xxi—Fe6—Nd1116.108 (3)
Fe6ii—Fe2—Nd2xiv65.229 (2)Fe6xvii—Fe6—Nd1112.023 (3)
Fe6xxi—Fe2—Nd2xiv114.771 (2)Fe6xxiv—Fe6—Nd1171.912 (3)
Fe6xxi—Fe2—Nd2xxvi65.229 (2)Fe6xxi—Fe6—Nd2xiv114.843 (3)
Fe6xxi—Fe2—Fe5xx120.305 (2)Fe6xvii—Fe6—Nd2xiv173.500 (3)
Fe6xxii—Fe2—Fe5xx57.968 (2)Fe6xxiv—Fe6—Nd2xiv114.464 (3)
Fe6xxi—Fe2—Fe5v122.032 (2)Fe6xxiv—Fe6—Fe4111.319 (3)
Fe6ii—Fe2—Fe5iv120.305 (2)Fe6xxiv—Fe6—Fe4xxiv61.721 (3)
Fe6xxii—Fe2—Fe5v59.695 (2)Fe6xxi—Fe6—Fe4112.524 (4)
Fe6xxi—Fe2—Fe5iv59.695 (2)Fe6xvii—Fe6—Fe4xxiv113.210 (4)
Fe6ii—Fe2—Fe5xix122.032 (2)Fe6xxi—Fe6—Fe4xxiv112.123 (4)
Fe6ii—Fe2—Fe5xx59.695 (2)Fe6xvii—Fe6—Fe460.834 (3)
Fe6—Fe2—Fe5v120.306 (2)Fe6xxi—Fe6—Fe6xvii60.026 (2)
Fe6—Fe2—Fe5iv57.969 (2)Fe6xxiv—Fe6—Fe6xvii59.948 (3)
Fe6ii—Fe2—Fe5v57.968 (2)Fe6xxi—Fe6—Fe6xxiv60.026 (1)
Fe6xxii—Fe2—Fe5xix120.305 (2)Fe1—B1—Nd1137.740 (19)
Fe6—Fe2—Fe5xix59.694 (2)Fe1xv—B1—Nd1137.740 (19)
Fe6xxii—Fe2—Fe5iv122.032 (2)Fe1—B1—Fe1xv84.52 (4)
Fe6—Fe2—Fe5xx122.031 (2)Fe1xv—B1—Fe5v73.056 (10)
Fe6xxi—Fe2—Fe5xix57.968 (2)Fe1—B1—Fe5v134.55 (3)
Fe6xxii—Fe2—Fe6ii61.364 (3)Fe1—B1—Fe5iii73.056 (10)
Fe6—Fe2—Fe6ii118.636 (3)Fe1—B1—Fe5iv73.056 (10)
Fe6ii—Fe2—Fe6xxi180.0Fe1xv—B1—Fe5vi73.056 (10)
Fe6—Fe2—Fe6xxi61.364 (3)Fe1xv—B1—Fe5iv134.55 (3)
Fe6xxii—Fe2—Fe6xxi118.636 (3)Fe1xv—B1—Fe5iii134.55 (3)
Fe6—Fe2—Fe6xxii180.0Fe1—B1—Fe5vi134.55 (3)
Nd1xvii—Fe3—Nd1xxvii65.418 (2)Fe5v—B1—Nd173.92 (3)
Nd2xxvii—Fe3—Nd1xxvii70.640 (2)Fe5iii—B1—Nd173.92 (3)
Nd2xxvii—Fe3—Nd1xvii70.640 (2)Fe5iv—B1—Nd173.92 (3)
Fe1—Fe3—Nd1xvii118.727 (3)Fe5vi—B1—Nd173.92 (3)
Fe1—Fe3—Nd1xxvii118.727 (3)Fe5iv—B1—Fe5iii75.911 (12)
Fe1—Fe3—Nd2xxvii168.367 (4)Fe5v—B1—Fe5vi75.911 (13)
Fe1—Fe3—Fe4iii64.914 (2)Fe5iii—B1—Fe5vi95.161 (17)
Fe1—Fe3—Fe4xvii64.914 (2)Fe5iii—B1—Fe5v147.84 (5)
Fe1—Fe3—Fe4108.591 (4)Fe5iv—B1—Fe5vi147.84 (5)
Fe1—Fe3—Fe5iv58.620 (3)Fe5iv—B1—Fe5v95.161 (17)
Fe1—Fe3—Fe5iii58.620 (3)
Symmetry codes: (i) y+1/2, x+1/2, z+1/2; (ii) x, y, z; (iii) y+1/2, x1/2, z+1/2; (iv) x1/2, y+1/2, z+1/2; (v) x1/2, y+1/2, z1/2; (vi) y+1/2, x1/2, z1/2; (vii) y, x, z; (viii) y, x, z; (ix) x+1, y, z; (x) y+1/2, x+1/2, z1/2; (xi) x+1/2, y+1/2, z1/2; (xii) x+1/2, y+1/2, z+1/2; (xiii) x+1, y+1, z; (xiv) x+1, y+1, z; (xv) x, y, z; (xvi) x, y, z; (xvii) y1/2, x+1/2, z+1/2; (xviii) x+1/2, y1/2, z+1/2; (xix) x+1/2, y+1/2, z+1/2; (xx) x+1/2, y+1/2, z1/2; (xxi) x, y+1, z; (xxii) x, y+1, z; (xxiii) y+1, x+1, z; (xxiv) y+1/2, x+1/2, z+1/2; (xxv) x+1, y, z; (xxvi) x1, y, z; (xxvii) y+1/2, x1/2, z+1/2.
(nd2fe14b_300k) top
Crystal data top
BFe14Nd2Dx = 7.569 Mg m3
Mr = 1081.19Synchrotron radiation, λ = 0.2482 Å
Tetragonal, P42/mnmCell parameters from 4168 reflections
a = 8.8143 (2) Åθ = 1.0–18.1°
c = 12.2117 (2) ŵ = 4.30 mm1
V = 948.75 (5) Å3T = 300 K
Z = 4Block, black
F(000) = 19560.13 × 0.06 × 0.03 mm
Data collection top
1/4-chi goniometer
diffractometer
Rint = 0.037
Absorption correction: multi-scan
SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.0775 before and 0.0590 after correction. The Ratio of minimum to maximum transmission is 0.7638. The λ/2 correction factor is Not present.
θmax = 18.1°, θmin = 1.0°
Tmin = 0.550, Tmax = 0.745h = 2222
142723 measured reflectionsk = 2222
4168 independent reflectionsl = 3030
4091 reflections with I > 2σ(I)
Refinement top
Refinement on F251 parameters
Least-squares matrix: full0 restraints
R[F2 > 2σ(F2)] = 0.008 w = 1/[σ2(Fo2) + (0.0101P)2]
where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.019(Δ/σ)max = 0.003
S = 1.12Δρmax = 0.62 e Å3
4168 reflectionsΔρmin = 1.75 e Å3
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Nd10.35691 (2)0.35691 (2)0.0000000.00667 (1)
Nd20.77022 (2)0.22978 (2)0.0000000.00650 (1)
Fe10.0000000.0000000.11501 (2)0.00552 (1)
Fe20.0000000.5000000.0000000.00622 (1)
Fe30.09804 (2)0.09804 (2)0.29525 (2)0.00644 (1)
Fe40.31746 (2)0.31746 (2)0.25424 (2)0.00650 (1)
Fe50.56700 (2)0.22459 (2)0.37236 (2)0.00619 (1)
Fe60.13995 (2)0.53692 (2)0.17605 (2)0.00578 (1)
B10.12437 (7)0.12437 (7)0.0000000.00833 (9)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Nd10.00688 (1)0.00688 (1)0.00626 (1)0.00093 (1)0.0000.000
Nd20.00709 (1)0.00709 (1)0.00533 (1)0.00128 (1)0.0000.000
Fe10.00543 (2)0.00543 (2)0.00569 (2)0.00081 (2)0.0000.000
Fe20.00746 (3)0.00617 (3)0.00503 (2)0.00012 (2)0.0000.000
Fe30.00626 (1)0.00626 (1)0.00681 (2)0.00035 (2)0.00031 (1)0.00031 (1)
Fe40.00668 (1)0.00668 (1)0.00614 (2)0.00037 (2)0.00020 (1)0.00020 (1)
Fe50.00634 (1)0.00522 (1)0.00700 (1)0.00022 (1)0.00021 (1)0.00065 (1)
Fe60.00563 (1)0.00580 (1)0.00592 (1)0.00019 (1)0.00033 (1)0.00003 (1)
B10.00962 (15)0.00962 (15)0.0057 (2)0.0014 (2)0.0000.000
Geometric parameters (Å, º) top
Nd1—Fe3i3.3056 (1)Fe1—B1xv2.0919 (7)
Nd1—Fe4ii3.1434 (1)Fe2—Fe5iii2.5879 (1)
Nd1—Fe43.1434 (1)Fe2—Fe5xix2.5879 (1)
Nd1—Fe5iii3.0782 (1)Fe2—Fe5xx2.5879 (1)
Nd1—Fe5iv3.0782 (1)Fe2—Fe5vi2.5879 (1)
Nd1—Fe5v3.0782 (1)Fe2—Fe6xxi2.4999 (1)
Nd1—Fe5vi3.0782 (1)Fe2—Fe6xxii2.4999 (1)
Nd1—Fe6vii3.2858 (1)Fe2—Fe62.4999 (1)
Nd1—Fe63.2858 (1)Fe2—Fe6ii2.4999 (1)
Nd1—Fe6ii3.2858 (1)Fe3—Fe3xvi2.4442 (2)
Nd1—Fe6viii3.2858 (1)Fe3—Fe4iv2.6527 (1)
Nd1—B12.8986 (9)Fe3—Fe42.7805 (1)
Nd2—Fe2ix3.1265 (1)Fe3—Fe4xvii2.6527 (1)
Nd2—Fe2viii3.1265 (1)Fe3—Fe5iv2.5901 (1)
Nd2—Fe4x3.0584 (1)Fe3—Fe5iii2.5901 (1)
Nd2—Fe4i3.0584 (1)Fe3—Fe6xviii2.3972 (1)
Nd2—Fe5xi3.0715 (1)Fe3—Fe6xvii2.3972 (1)
Nd2—Fe5x3.0715 (1)Fe4—Fe5vii2.7548 (1)
Nd2—Fe5i3.0715 (1)Fe4—Fe5iv2.7205 (1)
Nd2—Fe5xii3.0715 (1)Fe4—Fe5iii2.7205 (1)
Nd2—Fe6vii3.0786 (1)Fe4—Fe52.7548 (1)
Nd2—Fe6viii3.0786 (1)Fe4—Fe6xvii2.6420 (1)
Nd2—Fe6xiii3.0786 (1)Fe4—Fe6vii2.6649 (1)
Nd2—Fe6xiv3.0786 (1)Fe4—Fe6xviii2.6420 (1)
Fe1—Fe1xv2.8091 (2)Fe4—Fe62.6649 (1)
Fe1—Fe3xvi2.5175 (1)Fe5—Fe5xxiii2.5980 (1)
Fe1—Fe32.5175 (1)Fe5—Fe6vii2.5246 (1)
Fe1—Fe4iv2.7798 (1)Fe5—Fe6xviii2.5324 (1)
Fe1—Fe4xvii2.7798 (1)Fe5—Fe6xii2.4650 (1)
Fe1—Fe5xvii2.5031 (1)Fe5—B1i2.1113 (3)
Fe1—Fe5xviii2.5031 (1)Fe6—Fe6xxiv2.5529 (1)
Fe1—Fe5iii2.5031 (1)Fe6—Fe6xvii2.5529 (1)
Fe1—Fe5iv2.5031 (1)Fe6—Fe6xxii2.5516 (1)
Fe1—B12.0919 (7)
Fe4—Nd1—Fe3i48.496 (2)Fe3xvi—Fe3—Nd1xxvii68.302 (1)
Fe4ii—Nd1—Fe3i146.255 (2)Fe3xvi—Fe3—Nd1xvii68.302 (1)
Fe4—Nd1—Fe4ii161.998 (3)Fe3xvi—Fe3—Nd2xxvii130.642 (2)
Fe4—Nd1—Fe648.914 (1)Fe3xvi—Fe3—Fe160.958 (2)
Fe4—Nd1—Fe6vii48.914 (1)Fe3xvi—Fe3—Fe4xvii62.566 (2)
Fe4ii—Nd1—Fe6ii48.914 (1)Fe3xvi—Fe3—Fe4iv62.566 (2)
Fe4ii—Nd1—Fe6vii129.440 (1)Fe3xvi—Fe3—Fe4169.624 (2)
Fe4—Nd1—Fe6viii129.440 (2)Fe3xvi—Fe3—Fe5iii110.617 (2)
Fe4ii—Nd1—Fe6129.440 (1)Fe3xvi—Fe3—Fe5iv110.617 (2)
Fe4—Nd1—Fe6ii129.440 (2)Fe4iv—Fe3—Nd1xvii117.701 (3)
Fe4ii—Nd1—Fe6viii48.914 (1)Fe4—Fe3—Nd1xvii119.994 (2)
Fe5vi—Nd1—Fe3i160.876 (2)Fe4xvii—Fe3—Nd1xvii62.556 (2)
Fe5iii—Nd1—Fe3i100.298 (2)Fe4—Fe3—Nd1xxvii119.994 (2)
Fe5v—Nd1—Fe3i129.256 (2)Fe4iv—Fe3—Nd1xxvii62.556 (2)
Fe5iv—Nd1—Fe3i82.342 (2)Fe4xvii—Fe3—Nd1xxvii117.701 (3)
Fe5v—Nd1—Fe4ii51.846 (2)Fe4xvii—Fe3—Nd2xxvii118.226 (2)
Fe5iv—Nd1—Fe451.846 (2)Fe4iv—Fe3—Nd2xxvii118.226 (2)
Fe5iv—Nd1—Fe4ii112.487 (2)Fe4—Fe3—Nd2xxvii59.735 (2)
Fe5iii—Nd1—Fe451.846 (2)Fe4xvii—Fe3—Fe4114.340 (2)
Fe5v—Nd1—Fe4112.488 (2)Fe4iv—Fe3—Fe4114.340 (2)
Fe5iii—Nd1—Fe4ii112.487 (2)Fe4xvii—Fe3—Fe4iv118.143 (3)
Fe5vi—Nd1—Fe4112.488 (2)Fe5iii—Fe3—Nd1xvii117.213 (2)
Fe5vi—Nd1—Fe4ii51.846 (2)Fe5iv—Fe3—Nd1xxvii117.213 (2)
Fe5v—Nd1—Fe5vi49.921 (2)Fe5iii—Fe3—Nd1xxvii176.912 (3)
Fe5iv—Nd1—Fe5iii49.921 (2)Fe5iv—Fe3—Nd1xvii176.912 (3)
Fe5vi—Nd1—Fe5iii60.844 (3)Fe5iii—Fe3—Nd2xxvii111.733 (3)
Fe5v—Nd1—Fe5iv60.844 (3)Fe5iv—Fe3—Nd2xxvii111.733 (3)
Fe5v—Nd1—Fe5iii82.471 (2)Fe5iv—Fe3—Fe4xvii114.357 (3)
Fe5vi—Nd1—Fe5iv82.471 (2)Fe5iv—Fe3—Fe460.745 (2)
Fe5iii—Nd1—Fe6vii86.201 (2)Fe5iii—Fe3—Fe4iv114.357 (3)
Fe5iv—Nd1—Fe6vii45.431 (2)Fe5iii—Fe3—Fe4xvii63.383 (2)
Fe5iii—Nd1—Fe645.431 (1)Fe5iv—Fe3—Fe4iv63.383 (2)
Fe5iii—Nd1—Fe6viii126.611 (2)Fe5iii—Fe3—Fe460.745 (2)
Fe5iv—Nd1—Fe686.201 (2)Fe5iv—Fe3—Fe5iii60.202 (3)
Fe5v—Nd1—Fe6vii87.757 (2)Fe6xvii—Fe3—Nd1xxvii122.400 (3)
Fe5iv—Nd1—Fe6viii87.757 (2)Fe6xvii—Fe3—Nd1xvii68.233 (2)
Fe5iii—Nd1—Fe6ii87.757 (2)Fe6xviii—Fe3—Nd1xvii122.400 (3)
Fe5vi—Nd1—Fe687.757 (2)Fe6xviii—Fe3—Nd1xxvii68.233 (2)
Fe5vi—Nd1—Fe6vii126.611 (2)Fe6xviii—Fe3—Nd2xxvii63.183 (2)
Fe5v—Nd1—Fe6ii86.201 (2)Fe6xvii—Fe3—Nd2xxvii63.183 (2)
Fe5vi—Nd1—Fe6viii86.201 (2)Fe6xviii—Fe3—Fe1112.420 (2)
Fe5iv—Nd1—Fe6ii126.611 (2)Fe6xvii—Fe3—Fe1112.420 (2)
Fe5v—Nd1—Fe6126.610 (2)Fe6xvii—Fe3—Fe3xvi121.486 (2)
Fe5vi—Nd1—Fe6ii45.431 (1)Fe6xviii—Fe3—Fe3xvi121.486 (2)
Fe5v—Nd1—Fe6viii45.431 (2)Fe6xviii—Fe3—Fe460.829 (2)
Fe6viii—Nd1—Fe3i104.734 (2)Fe6xviii—Fe3—Fe4iv63.466 (2)
Fe6vii—Nd1—Fe3i42.652 (2)Fe6xviii—Fe3—Fe4xvii174.054 (4)
Fe6ii—Nd1—Fe3i144.204 (2)Fe6xvii—Fe3—Fe460.829 (2)
Fe6—Nd1—Fe3i79.705 (2)Fe6xvii—Fe3—Fe4xvii63.466 (2)
Fe6viii—Nd1—Fe6ii97.700 (2)Fe6xvii—Fe3—Fe4iv174.054 (4)
Fe6viii—Nd1—Fe6vii81.732 (2)Fe6xvii—Fe3—Fe5iv110.671 (3)
Fe6ii—Nd1—Fe6vii171.964 (2)Fe6xviii—Fe3—Fe5iv60.678 (2)
Fe6viii—Nd1—Fe6171.963 (2)Fe6xvii—Fe3—Fe5iii60.678 (2)
Fe6ii—Nd1—Fe681.732 (3)Fe6xviii—Fe3—Fe5iii110.671 (3)
Fe6vii—Nd1—Fe697.700 (3)Fe6xviii—Fe3—Fe6xvii114.309 (4)
B1—Nd1—Fe3i122.656 (1)Fe1i—Fe4—Fe3134.567 (4)
B1—Nd1—Fe480.999 (2)Fe3xxiv—Fe4—Fe1i55.156 (3)
B1—Nd1—Fe4ii80.999 (2)Fe3i—Fe4—Fe1i55.156 (3)
B1—Nd1—Fe5v41.236 (1)Fe3xxiv—Fe4—Fe3152.229 (2)
B1—Nd1—Fe5iii41.236 (1)Fe3xxiv—Fe4—Fe3i54.866 (3)
B1—Nd1—Fe5iv41.236 (1)Fe3i—Fe4—Fe3152.229 (2)
B1—Nd1—Fe5vi41.236 (1)Fe3xxiv—Fe4—Fe5iii103.027 (3)
B1—Nd1—Fe685.982 (1)Fe3i—Fe4—Fe5iii131.711 (4)
B1—Nd1—Fe6vii85.982 (1)Fe3i—Fe4—Fe5vii99.912 (3)
B1—Nd1—Fe6ii85.982 (1)Fe3xxiv—Fe4—Fe5iv131.711 (4)
B1—Nd1—Fe6viii85.982 (1)Fe3xxiv—Fe4—Fe599.912 (3)
Fe2ix—Nd2—Fe2viii170.751 (1)Fe3i—Fe4—Fe5iv103.027 (3)
Fe4i—Nd2—Fe2viii90.9Fe3i—Fe4—Fe557.201 (2)
Fe4i—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe5vii57.201 (2)
Fe4x—Nd2—Fe2ix90.9Fe3xxiv—Fe4—Fe653.591 (2)
Fe4x—Nd2—Fe2viii90.9Fe3xxiv—Fe4—Fe6vii105.185 (3)
Fe4x—Nd2—Fe4i157.801 (3)Fe3i—Fe4—Fe6105.186 (3)
Fe4x—Nd2—Fe5x53.410 (2)Fe3i—Fe4—Fe6vii53.591 (2)
Fe4i—Nd2—Fe5i53.410 (2)Fe5—Fe4—Fe1i53.777 (2)
Fe4i—Nd2—Fe5xi113.570 (2)Fe5vii—Fe4—Fe1i53.777 (2)
Fe4i—Nd2—Fe5x113.570 (2)Fe5iv—Fe4—Fe1i151.041 (2)
Fe4x—Nd2—Fe5i113.570 (2)Fe5iii—Fe4—Fe1i151.041 (2)
Fe4x—Nd2—Fe5xi53.410 (2)Fe5—Fe4—Fe3104.736 (3)
Fe4i—Nd2—Fe5xii53.410 (2)Fe5iii—Fe4—Fe356.164 (2)
Fe4x—Nd2—Fe5xii113.570 (2)Fe5iv—Fe4—Fe356.164 (2)
Fe4i—Nd2—Fe6vii50.998 (2)Fe5vii—Fe4—Fe3104.735 (3)
Fe4x—Nd2—Fe6xiii137.833 (1)Fe5iii—Fe4—Fe5vii99.508 (2)
Fe4x—Nd2—Fe6vii137.833 (1)Fe5—Fe4—Fe5vii101.556 (3)
Fe4x—Nd2—Fe6xiv50.998 (2)Fe5iv—Fe4—Fe5vii154.825 (2)
Fe4x—Nd2—Fe6viii50.998 (2)Fe5iii—Fe4—Fe5iv57.043 (3)
Fe4i—Nd2—Fe6xiv137.833 (1)Fe5iv—Fe4—Fe599.509 (2)
Fe4i—Nd2—Fe6viii137.833 (1)Fe5iii—Fe4—Fe5154.826 (2)
Fe4i—Nd2—Fe6xiii50.998 (2)Fe6xvii—Fe4—Fe1i105.927 (3)
Fe5xi—Nd2—Fe2viii137.193 (1)Fe6vii—Fe4—Fe1i97.208 (2)
Fe5i—Nd2—Fe2ix137.193 (2)Fe6xviii—Fe4—Fe1i105.927 (3)
Fe5x—Nd2—Fe2viii49.348 (1)Fe6—Fe4—Fe1i97.208 (2)
Fe5xii—Nd2—Fe2ix49.348 (1)Fe6xviii—Fe4—Fe3i101.755 (2)
Fe5xii—Nd2—Fe2viii137.193 (2)Fe6xviii—Fe4—Fe352.397 (2)
Fe5x—Nd2—Fe2ix137.193 (2)Fe6—Fe4—Fe399.268 (2)
Fe5xi—Nd2—Fe2ix49.348 (1)Fe6xviii—Fe4—Fe3xxiv154.975 (3)
Fe5i—Nd2—Fe2viii49.348 (1)Fe6vii—Fe4—Fe399.269 (2)
Fe5x—Nd2—Fe5xi88.025 (2)Fe6xvii—Fe4—Fe3i154.975 (3)
Fe5xi—Nd2—Fe5i118.724 (2)Fe6xvii—Fe4—Fe352.397 (2)
Fe5xii—Nd2—Fe5xi60.991 (2)Fe6xvii—Fe4—Fe3xxiv101.755 (2)
Fe5xii—Nd2—Fe5x118.724 (2)Fe6xvii—Fe4—Fe5vii55.924 (2)
Fe5x—Nd2—Fe5i60.991 (2)Fe6xviii—Fe4—Fe5iii99.842 (3)
Fe5xii—Nd2—Fe5i88.025 (2)Fe6vii—Fe4—Fe555.498 (2)
Fe5xi—Nd2—Fe6vii163.127 (2)Fe6vii—Fe4—Fe5iii107.787 (3)
Fe5x—Nd2—Fe6xiii163.127 (2)Fe6xvii—Fe4—Fe5iii56.149 (2)
Fe5i—Nd2—Fe6xiii104.370 (3)Fe6vii—Fe4—Fe5iv54.468 (2)
Fe5i—Nd2—Fe6vii48.632 (2)Fe6—Fe4—Fe5150.702 (4)
Fe5xi—Nd2—Fe6xiii92.744 (2)Fe6xvii—Fe4—Fe5iv99.842 (3)
Fe5i—Nd2—Fe6viii92.744 (2)Fe6vii—Fe4—Fe5vii150.703 (3)
Fe5xii—Nd2—Fe6xiii48.632 (2)Fe6xviii—Fe4—Fe5iv56.149 (2)
Fe5x—Nd2—Fe6vii92.744 (2)Fe6—Fe4—Fe5iv107.787 (3)
Fe5xii—Nd2—Fe6xiv92.744 (2)Fe6xviii—Fe4—Fe555.924 (2)
Fe5i—Nd2—Fe6xiv163.127 (2)Fe6xviii—Fe4—Fe5vii128.374 (3)
Fe5xii—Nd2—Fe6vii104.370 (2)Fe6xvii—Fe4—Fe5128.373 (3)
Fe5xii—Nd2—Fe6viii163.127 (2)Fe6—Fe4—Fe5iii54.468 (2)
Fe5xi—Nd2—Fe6viii104.370 (2)Fe6—Fe4—Fe5vii55.497 (2)
Fe5x—Nd2—Fe6xiv104.370 (2)Fe6xvii—Fe4—Fe6vii151.434 (3)
Fe5xi—Nd2—Fe6xiv48.632 (2)Fe6vii—Fe4—Fe6136.385 (4)
Fe5x—Nd2—Fe6viii48.632 (2)Fe6xvii—Fe4—Fe6xviii99.331 (3)
Fe6xiii—Nd2—Fe2ix47.509 (1)Fe6xvii—Fe4—Fe657.507 (2)
Fe6vii—Nd2—Fe2viii47.509 (1)Fe6xviii—Fe4—Fe6151.434 (3)
Fe6viii—Nd2—Fe2ix128.949 (1)Fe6xviii—Fe4—Fe6vii57.508 (2)
Fe6vii—Nd2—Fe2ix128.949 (1)Nd2xxvii—Fe5—Nd1i118.724 (3)
Fe6xiv—Nd2—Fe2viii128.949 (1)Fe1i—Fe5—Nd1i113.015 (2)
Fe6xiv—Nd2—Fe2ix47.509 (1)Fe1i—Fe5—Nd2xxvii68.951 (2)
Fe6xiii—Nd2—Fe2viii128.949 (1)Fe1i—Fe5—Fe2xviii130.612 (3)
Fe6viii—Nd2—Fe2viii47.509 (1)Fe1i—Fe5—Fe3i59.216 (3)
Fe6viii—Nd2—Fe6xiv81.715 (2)Fe1i—Fe5—Fe463.622 (2)
Fe6xiii—Nd2—Fe6xiv88.587 (2)Fe1i—Fe5—Fe4i111.011 (3)
Fe6xiii—Nd2—Fe6vii81.715 (2)Fe1i—Fe5—Fe5xxiii58.739 (1)
Fe6vii—Nd2—Fe6xiv146.227 (3)Fe1i—Fe5—Fe6xviii118.550 (2)
Fe6viii—Nd2—Fe6xiii146.227 (3)Fe1i—Fe5—Fe6vii108.680 (3)
Fe6viii—Nd2—Fe6vii88.587 (2)Fe2xviii—Fe5—Nd1i72.898 (2)
Fe1xv—Fe1—Nd2xxv63.879 (2)Fe2xviii—Fe5—Nd2xxvii66.433 (1)
Fe3—Fe1—Nd2xxv112.638 (2)Fe2xviii—Fe5—Fe3i164.116 (2)
Fe3xvi—Fe1—Nd2xxv112.638 (2)Fe2xviii—Fe5—Fe4i115.040 (3)
Fe3xvi—Fe1—Fe1xv150.958 (2)Fe2xviii—Fe5—Fe4111.131 (3)
Fe3—Fe1—Fe1xv150.958 (2)Fe2xviii—Fe5—Fe5xxiii134.608 (1)
Fe3xvi—Fe1—Fe358.084 (4)Fe3i—Fe5—Nd1i116.956 (2)
Fe3xvi—Fe1—Fe4xvii59.857 (2)Fe3i—Fe5—Nd2xxvii114.328 (3)
Fe3—Fe1—Fe4xvii59.857 (2)Fe3i—Fe5—Fe4i63.091 (3)
Fe3xvi—Fe1—Fe4iv59.857 (2)Fe3i—Fe5—Fe459.416 (2)
Fe3—Fe1—Fe4iv59.857 (2)Fe3i—Fe5—Fe5xxiii59.899 (2)
Fe4iv—Fe1—Nd2xxv61.178 (2)Fe4i—Fe5—Nd1i65.312 (3)
Fe4xvii—Fe1—Nd2xxv171.065 (4)Fe4—Fe5—Nd1i175.800 (3)
Fe4xvii—Fe1—Fe1xv125.057 (2)Fe4—Fe5—Nd2xxvii63.052 (2)
Fe4iv—Fe1—Fe1xv125.057 (2)Fe4i—Fe5—Nd2xxvii175.813 (2)
Fe4iv—Fe1—Fe4xvii109.887 (5)Fe4i—Fe5—Fe4113.006 (2)
Fe5xvii—Fe1—Nd2xxv119.542 (2)Fe5xxiii—Fe5—Nd1i65.039 (1)
Fe5iii—Fe1—Nd2xxv119.542 (2)Fe5xxiii—Fe5—Nd2xxvii120.639 (2)
Fe5iv—Fe1—Nd2xxv63.971 (1)Fe5xxiii—Fe5—Fe4i61.479 (1)
Fe5xviii—Fe1—Nd2xxv63.971 (2)Fe5xxiii—Fe5—Fe4110.762 (2)
Fe5xvii—Fe1—Fe1xv93.532 (3)Fe6xii—Fe5—Nd1i71.739 (2)
Fe5iv—Fe1—Fe1xv93.532 (3)Fe6vii—Fe5—Nd1i119.936 (2)
Fe5iii—Fe1—Fe1xv93.532 (3)Fe6xviii—Fe5—Nd1i124.314 (2)
Fe5xviii—Fe1—Fe1xv93.532 (3)Fe6xii—Fe5—Nd2xxvii117.797 (2)
Fe5iv—Fe1—Fe3xvi111.102 (4)Fe6xviii—Fe5—Nd2xxvii65.829 (2)
Fe5iii—Fe1—Fe362.112 (2)Fe6vii—Fe5—Nd2xxvii115.540 (2)
Fe5xviii—Fe1—Fe3111.102 (4)Fe6xii—Fe5—Fe1i169.483 (4)
Fe5xviii—Fe1—Fe3xvi62.113 (2)Fe6vii—Fe5—Fe2xviii108.780 (3)
Fe5iv—Fe1—Fe362.112 (2)Fe6xviii—Fe5—Fe2xviii58.437 (2)
Fe5xvii—Fe1—Fe3xvi62.113 (2)Fe6xii—Fe5—Fe2xviii59.247 (2)
Fe5xvii—Fe1—Fe3111.102 (4)Fe6xviii—Fe5—Fe3i106.613 (3)
Fe5iii—Fe1—Fe3xvi111.102 (4)Fe6xii—Fe5—Fe3i110.327 (3)
Fe5xvii—Fe1—Fe4xvii62.601 (2)Fe6vii—Fe5—Fe3i55.880 (2)
Fe5xviii—Fe1—Fe4xvii112.918 (3)Fe6xii—Fe5—Fe4i61.617 (2)
Fe5xviii—Fe1—Fe4iv62.601 (2)Fe6vii—Fe5—Fe4i60.353 (2)
Fe5iii—Fe1—Fe4iv112.918 (3)Fe6xviii—Fe5—Fe459.784 (2)
Fe5iii—Fe1—Fe4xvii62.601 (2)Fe6vii—Fe5—Fe460.445 (2)
Fe5iv—Fe1—Fe4xvii112.918 (3)Fe6xviii—Fe5—Fe4i111.277 (3)
Fe5xvii—Fe1—Fe4iv112.918 (3)Fe6xii—Fe5—Fe4111.136 (3)
Fe5iv—Fe1—Fe4iv62.601 (2)Fe6xviii—Fe5—Fe5xxiii166.219 (2)
Fe5iii—Fe1—Fe5iv62.523 (3)Fe6vii—Fe5—Fe5xxiii106.451 (2)
Fe5xviii—Fe1—Fe5xvii62.523 (2)Fe6xii—Fe5—Fe5xxiii118.473 (2)
Fe5iv—Fe1—Fe5xvii172.937 (5)Fe6xii—Fe5—Fe6xviii61.388 (2)
Fe5iii—Fe1—Fe5xviii172.937 (5)Fe6vii—Fe5—Fe6xviii60.639 (2)
Fe5iii—Fe1—Fe5xvii116.988 (2)Fe6xii—Fe5—Fe6vii61.534 (2)
Fe5iv—Fe1—Fe5xviii116.988 (2)B1i—Fe5—Nd1i64.82 (2)
B1xv—Fe1—Nd2xxv72.807 (6)B1i—Fe5—Nd2xxvii75.331 (16)
B1—Fe1—Nd2xxv72.807 (6)B1i—Fe5—Fe1i53.09 (2)
B1—Fe1—Fe1xv47.825 (17)B1i—Fe5—Fe2xviii95.299 (9)
B1xv—Fe1—Fe1xv47.825 (17)B1i—Fe5—Fe3i100.223 (10)
B1xv—Fe1—Fe3xvi103.134 (17)B1i—Fe5—Fe4i108.123 (15)
B1xv—Fe1—Fe3161.217 (17)B1i—Fe5—Fe4112.98 (2)
B1—Fe1—Fe3103.133 (17)B1i—Fe5—Fe5xxiii52.031 (6)
B1—Fe1—Fe3xvi161.216 (17)B1i—Fe5—Fe6xviii139.178 (10)
B1—Fe1—Fe4iv112.683 (8)B1i—Fe5—Fe6xii134.77 (2)
B1—Fe1—Fe4xvii112.683 (8)B1i—Fe5—Fe6vii155.852 (7)
B1xv—Fe1—Fe4xvii112.684 (8)Nd2xiv—Fe6—Nd173.498 (2)
B1xv—Fe1—Fe4iv112.684 (8)Fe2—Fe6—Nd170.223 (2)
B1—Fe1—Fe5iv53.808 (13)Fe2—Fe6—Nd2xiv67.251 (2)
B1xv—Fe1—Fe5iii132.315 (12)Fe2—Fe6—Fe4xxiv117.973 (3)
B1xv—Fe1—Fe5xviii53.808 (13)Fe2—Fe6—Fe4120.221 (3)
B1xv—Fe1—Fe5xvii53.808 (13)Fe2—Fe6—Fe5vii167.443 (3)
B1—Fe1—Fe5iii53.808 (13)Fe2—Fe6—Fe5xix61.891 (2)
B1—Fe1—Fe5xvii132.315 (12)Fe2—Fe6—Fe6xxiv110.695 (3)
B1—Fe1—Fe5xviii132.315 (12)Fe2—Fe6—Fe6xvii110.695 (2)
B1xv—Fe1—Fe5iv132.315 (12)Fe2—Fe6—Fe6xxii59.314 (2)
B1xv—Fe1—B195.65 (3)Fe3xxiv—Fe6—Nd169.114 (2)
Nd1—Fe2—Nd1xxi180.0Fe3xxiv—Fe6—Nd2xiv72.795 (2)
Nd2xxvi—Fe2—Nd1108.529 (1)Fe3xxiv—Fe6—Fe2129.077 (3)
Nd2xxvi—Fe2—Nd1xxi71.471 (1)Fe3xxiv—Fe6—Fe462.943 (3)
Nd2xiv—Fe2—Nd1xxi108.529 (1)Fe3xxiv—Fe6—Fe4xxiv66.775 (2)
Nd2xiv—Fe2—Nd171.471 (1)Fe3xxiv—Fe6—Fe5vii63.442 (2)
Nd2xxvi—Fe2—Nd2xiv180.0Fe3xxiv—Fe6—Fe5iii119.770 (3)
Fe5xx—Fe2—Nd1xxi60.234 (2)Fe3xxiv—Fe6—Fe5xix125.541 (3)
Fe5xix—Fe2—Nd1119.766 (2)Fe3xxiv—Fe6—Fe6xvii112.117 (3)
Fe5iii—Fe2—Nd1xxi119.766 (2)Fe3xxiv—Fe6—Fe6xxiv113.887 (3)
Fe5vi—Fe2—Nd160.234 (2)Fe3xxiv—Fe6—Fe6xxii171.434 (2)
Fe5xix—Fe2—Nd1xxi60.234 (2)Fe4—Fe6—Nd162.754 (2)
Fe5iii—Fe2—Nd160.234 (2)Fe4xxiv—Fe6—Nd1125.456 (2)
Fe5vi—Fe2—Nd1xxi119.766 (2)Fe4—Fe6—Nd2xiv125.737 (2)
Fe5xx—Fe2—Nd1119.766 (2)Fe4xxiv—Fe6—Nd2xiv64.106 (3)
Fe5vi—Fe2—Nd2xxvi64.220 (2)Fe4xxiv—Fe6—Fe4118.719 (2)
Fe5vi—Fe2—Nd2xiv115.780 (2)Fe5xix—Fe6—Nd1125.584 (3)
Fe5xx—Fe2—Nd2xiv64.220 (1)Fe5vii—Fe6—Nd1120.001 (3)
Fe5xix—Fe2—Nd2xxvi115.780 (2)Fe5iii—Fe6—Nd162.829 (2)
Fe5xix—Fe2—Nd2xiv64.220 (2)Fe5vii—Fe6—Nd2xiv121.129 (2)
Fe5xx—Fe2—Nd2xxvi115.780 (1)Fe5xix—Fe6—Nd2xiv65.539 (2)
Fe5iii—Fe2—Nd2xxvi64.220 (1)Fe5iii—Fe6—Nd2xiv121.616 (3)
Fe5iii—Fe2—Nd2xiv115.780 (1)Fe5iii—Fe6—Fe262.825 (2)
Fe5vi—Fe2—Fe5iii74.072 (3)Fe5xix—Fe6—Fe4168.723 (3)
Fe5vi—Fe2—Fe5xx105.928 (3)Fe5iii—Fe6—Fe463.915 (3)
Fe5vi—Fe2—Fe5xix180.0Fe5vii—Fe6—Fe464.057 (2)
Fe5xix—Fe2—Fe5iii105.928 (3)Fe5iii—Fe6—Fe4xxiv171.711 (3)
Fe5xx—Fe2—Fe5iii180.0Fe5vii—Fe6—Fe4xxiv63.498 (3)
Fe5xix—Fe2—Fe5xx74.072 (3)Fe5xix—Fe6—Fe4xxiv64.293 (2)
Fe6—Fe2—Nd1xxi114.177 (1)Fe5iii—Fe6—Fe5vii113.766 (2)
Fe6ii—Fe2—Nd1xxi114.178 (2)Fe5iii—Fe6—Fe5xix111.525 (3)
Fe6—Fe2—Nd165.823 (2)Fe5vii—Fe6—Fe5xix111.465 (2)
Fe6ii—Fe2—Nd165.822 (1)Fe5iii—Fe6—Fe6xvii60.384 (2)
Fe6xxii—Fe2—Nd1xxi65.822 (2)Fe5xix—Fe6—Fe6xxii58.004 (2)
Fe6xxii—Fe2—Nd1114.178 (1)Fe5vii—Fe6—Fe6xxii108.211 (2)
Fe6xxi—Fe2—Nd1114.178 (1)Fe5vii—Fe6—Fe6xvii59.831 (3)
Fe6xxi—Fe2—Nd1xxi65.822 (2)Fe5vii—Fe6—Fe6xxiv58.083 (3)
Fe6xxi—Fe2—Nd2xiv114.761 (2)Fe5xix—Fe6—Fe6xxiv59.531 (2)
Fe6xxi—Fe2—Nd2xxvi65.239 (2)Fe5iii—Fe6—Fe6xxii60.609 (2)
Fe6xxii—Fe2—Nd2xxvi65.239 (2)Fe5xix—Fe6—Fe6xvii107.928 (2)
Fe6ii—Fe2—Nd2xiv65.239 (2)Fe5iii—Fe6—Fe6xxiv110.061 (2)
Fe6ii—Fe2—Nd2xxvi114.761 (2)Fe6xxii—Fe6—Nd1116.076 (2)
Fe6xxii—Fe2—Nd2xiv114.761 (2)Fe6xvii—Fe6—Nd1112.026 (3)
Fe6—Fe2—Nd2xiv65.240 (2)Fe6xxiv—Fe6—Nd1171.927 (2)
Fe6—Fe2—Nd2xxvi114.760 (2)Fe6xxii—Fe6—Nd2xiv114.776 (2)
Fe6—Fe2—Fe5xx122.073 (2)Fe6xvii—Fe6—Nd2xiv173.446 (2)
Fe6ii—Fe2—Fe5xx59.672 (2)Fe6xxiv—Fe6—Nd2xiv114.425 (3)
Fe6—Fe2—Fe5vi120.329 (2)Fe6xxiv—Fe6—Fe4111.302 (3)
Fe6xxii—Fe2—Fe5iii59.672 (2)Fe6xxiv—Fe6—Fe4xxiv61.697 (2)
Fe6ii—Fe2—Fe5vi57.927 (2)Fe6xxii—Fe6—Fe4112.491 (3)
Fe6—Fe2—Fe5iii57.927 (2)Fe6xvii—Fe6—Fe4xxiv113.213 (3)
Fe6xxii—Fe2—Fe5xix57.927 (2)Fe6xxii—Fe6—Fe4xxiv112.096 (3)
Fe6xxii—Fe2—Fe5xx120.328 (2)Fe6xvii—Fe6—Fe460.796 (3)
Fe6xxi—Fe2—Fe5vi59.672 (2)Fe6xxii—Fe6—Fe6xvii60.018 (1)
Fe6xxi—Fe2—Fe5iii122.073 (2)Fe6xxiv—Fe6—Fe6xvii59.966 (2)
Fe6xxii—Fe2—Fe5vi122.073 (2)Fe6xxii—Fe6—Fe6xxiv60.018 (1)
Fe6ii—Fe2—Fe5xix122.073 (2)Fe1—B1—Nd1137.825 (17)
Fe6xxi—Fe2—Fe5xix120.328 (2)Fe1xv—B1—Nd1137.825 (17)
Fe6ii—Fe2—Fe5iii120.328 (2)Fe1—B1—Fe1xv84.35 (3)
Fe6xxi—Fe2—Fe5xx57.927 (2)Fe1xv—B1—Fe5vi73.097 (9)
Fe6—Fe2—Fe5xix59.671 (2)Fe1—B1—Fe5vi134.47 (3)
Fe6ii—Fe2—Fe6xxii180.0Fe1—B1—Fe5iv73.098 (9)
Fe6xxi—Fe2—Fe6xxii118.628 (3)Fe1—B1—Fe5iii73.098 (9)
Fe6xxii—Fe2—Fe661.372 (3)Fe1xv—B1—Fe5v73.097 (9)
Fe6xxi—Fe2—Fe6180.0Fe1xv—B1—Fe5iii134.47 (3)
Fe6ii—Fe2—Fe6118.628 (3)Fe1xv—B1—Fe5iv134.47 (3)
Fe6xxi—Fe2—Fe6ii61.373 (3)Fe1—B1—Fe5v134.47 (3)
Nd1xvii—Fe3—Nd1xxvii65.312 (2)Fe5vi—B1—Nd173.95 (2)
Nd2xxvii—Fe3—Nd1xxvii70.540 (2)Fe5iv—B1—Nd173.95 (2)
Nd2xxvii—Fe3—Nd1xvii70.540 (2)Fe5iii—B1—Nd173.95 (2)
Fe1—Fe3—Nd1xvii118.804 (3)Fe5v—B1—Nd173.95 (2)
Fe1—Fe3—Nd1xxvii118.804 (3)Fe5iii—B1—Fe5iv75.939 (11)
Fe1—Fe3—Nd2xxvii168.400 (3)Fe5vi—B1—Fe5v75.939 (11)
Fe1—Fe3—Fe4iv64.987 (2)Fe5iv—B1—Fe5v95.166 (15)
Fe1—Fe3—Fe4xvii64.987 (2)Fe5iv—B1—Fe5vi147.90 (5)
Fe1—Fe3—Fe4108.666 (3)Fe5iii—B1—Fe5v147.90 (5)
Fe1—Fe3—Fe5iv58.672 (3)Fe5iii—B1—Fe5vi95.166 (15)
Fe1—Fe3—Fe5iii58.672 (3)
Symmetry codes: (i) y+1/2, x+1/2, z+1/2; (ii) x, y, z; (iii) x1/2, y+1/2, z+1/2; (iv) y+1/2, x1/2, z+1/2; (v) y+1/2, x1/2, z1/2; (vi) x1/2, y+1/2, z1/2; (vii) y, x, z; (viii) y, x, z; (ix) x+1, y, z; (x) y+1/2, x+1/2, z1/2; (xi) x+1/2, y+1/2, z1/2; (xii) x+1/2, y+1/2, z+1/2; (xiii) x+1, y+1, z; (xiv) x+1, y+1, z; (xv) x, y, z; (xvi) x, y, z; (xvii) y1/2, x+1/2, z+1/2; (xviii) x+1/2, y1/2, z+1/2; (xix) x+1/2, y+1/2, z+1/2; (xx) x+1/2, y+1/2, z1/2; (xxi) x, y+1, z; (xxii) x, y+1, z; (xxiii) y+1, x+1, z; (xxiv) y+1/2, x+1/2, z+1/2; (xxv) x+1, y, z; (xxvi) x1, y, z; (xxvii) y+1/2, x1/2, z+1/2.
(XD) top
Crystal data top
BFe14Nd2Dx = 7.585 Mg m3
Mr = 1081.19Synchrotron radiation, λ = 0.2482 Å
Tetragonal, P42/mnmCell parameters from 6921 reflections
a = 8.8128 (2) Åθ = 1.8–21.9°
c = 12.1904 (3) ŵ = 4.31 mm1
V = 946.77 (4) Å3T = 25 K
Z = 4Block, black
F(000) = 19560.13 × 0.06 × 0.03 mm
Data collection top
1/4-chi goniometer
diffractometer
θmax = 21.9°, θmin = 1.8°
Absorption correction: multi-scan
SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.0775 before and 0.0590 after correction. The Ratio of minimum to maximum transmission is 0.7638. The λ/2 correction factor is Not present.
h = 2625
Tmin = 0.562, Tmax = 0.745k = 2625
473257 measured reflectionsl = 3636
Rint = 0.050
Refinement top
Refinement on F26921 reflections
Least-squares matrix: full125 parameters
R[F2 > 2σ(F2)] = 0.010 restraints
wR(F2) = 0.03 w2 = 1/[s2(Fo2)]
S = 1.00(Δ/σ)max < 0.001
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Nd(1)0.3569510.35695100.002
Nd(2)0.2298550.77014600.002
Nd(1B)0.3569510.35695100.002
Nd(2B)0.2298550.77014600.002
Fe(1)000.1156530.002
Fe(2)00.500.002
Fe(3)0.0980170.0980170.2960310.002
Fe(4)0.3175720.3175720.2541580.002
Fe(5)0.5671110.2249310.3722720.002
Fe(6)0.1396920.5368480.1760150.002
Fe(1B)000.1156530.002
Fe(2B)00.500.002
Fe(3B)0.0980170.0980170.2960310.002
Fe(4B)0.3175720.3175720.2541580.002
Fe(5B)0.5671110.2249310.3722720.002
Fe(6B)0.1396920.5368480.1760150.002
B(1)0.1239330.12393300.004
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Nd(1)0.001620.001620.0015880.00010200
Nd(2)0.0016670.0016670.0014550.0002200
Nd(1B)0.001620.001620.0015880.00010200
Nd(2B)0.0016670.0016670.0014550.0002200
Fe(1)0.001910.001910.002040.00014800
Fe(2)0.0023430.0020410.001887000
Fe(3)0.0020650.0020650.0022870.0000790.0000830.000083
Fe(4)0.0021520.0021520.0020780.0000860.0000510.000051
Fe(5)0.0021010.0018560.0022640.0000460.0000310.000135
Fe(6)0.0019430.0019880.0020460.0000370.0000740.000007
Fe(1B)0.001910.001910.002040.00014800
Fe(2B)0.0023430.0020410.001887000
Fe(3B)0.0020650.0020650.0022870.0000790.0000830.000083
Fe(4B)0.0021520.0021520.0020780.0000860.0000510.000051
Fe(5B)0.0021010.0018560.0022640.0000460.0000310.000135
Fe(6B)0.0019430.0019880.0020460.0000370.0000740.000007
B(1)0.0049430.0049430.0033960.00020900
Geometric parameters (Å, º) top
ND(1)—ND(1)i3.5657FE(2)—FE(6B)xix2.4950
ND(1)—ND(1)ii3.5657FE(3)—FE(3)ix2.4432
ND(1)—ND(1)iii3.5657FE(3)—FE(3)x2.4432
ND(1)—ND(1)iv3.5657FE(3)—FE(6)xii2.3979
ND(1)—ND(1B)i3.5657FE(3)—FE(6)xiv2.3979
ND(1)—ND(1B)ii3.5657FE(3)—FE(1B)2.5154
ND(1)—ND(1B)iii3.5657FE(3)—FE(1B)ix2.5154
ND(1)—ND(1B)iv3.5657FE(3)—FE(1B)x2.5154
ND(2)—FE(4)v3.0547FE(3)—FE(1B)xi2.5154
ND(2)—FE(4)vi3.0547FE(3)—FE(3B)ix2.4432
ND(2)—FE(4)vii3.0547FE(3)—FE(3B)x2.4432
ND(2)—FE(4)viii3.0547FE(3)—FE(6B)xii2.3979
ND(2)—FE(4B)v3.0547FE(3)—FE(6B)xiv2.3979
ND(2)—FE(4B)vi3.0547FE(5)—FE(6)xxii2.4653
ND(2)—FE(4B)vii3.0547FE(5)—FE(1B)vi2.4996
ND(2)—FE(4B)viii3.0547FE(5)—FE(1B)xxii2.4996
ND(1B)—ND(1B)i3.5657FE(5)—FE(1B)xxiii2.4996
ND(1B)—ND(1B)ii3.5657FE(5)—FE(1B)vii2.4996
ND(1B)—ND(1B)iii3.5657FE(5)—FE(6B)xxii2.4653
ND(1B)—ND(1B)iv3.5657FE(5)—B(1)xxiv2.1093
ND(2B)—FE(4)v3.0547FE(5)—B(1)xxii2.1093
ND(2B)—FE(4)vi3.0547FE(5)—B(1)xxiii2.1093
ND(2B)—FE(4)vii3.0547FE(5)—B(1)xxv2.1093
ND(2B)—FE(4)viii3.0547FE(6)—FE(2B)2.4950
ND(2B)—FE(4B)v3.0547FE(6)—FE(2B)xx2.4950
ND(2B)—FE(4B)vi3.0547FE(6)—FE(2B)xxi2.4950
ND(2B)—FE(4B)vii3.0547FE(6)—FE(2B)xix2.4950
ND(2B)—FE(4B)viii3.0547FE(6)—FE(3B)vi2.3979
FE(1)—FE(3)2.5154FE(6)—FE(3B)vii2.3979
FE(1)—FE(3)ix2.5154FE(6)—FE(5B)xiii2.4653
FE(1)—FE(3)x2.5154FE(1B)—FE(3B)2.5154
FE(1)—FE(3)xi2.5154FE(1B)—FE(3B)ix2.5154
FE(1)—FE(5)xii2.4996FE(1B)—FE(3B)x2.5154
FE(1)—FE(5)xiii2.4996FE(1B)—FE(3B)xi2.5154
FE(1)—FE(5)xiv2.4996FE(1B)—FE(5B)xii2.4996
FE(1)—FE(5)xv2.4996FE(1B)—FE(5B)xiii2.4996
FE(1)—FE(3B)2.5154FE(1B)—FE(5B)xiv2.4996
FE(1)—FE(3B)ix2.5154FE(1B)—FE(5B)xv2.4996
FE(1)—FE(3B)x2.5154FE(1B)—B(1)2.0913
FE(1)—FE(3B)xi2.5154FE(1B)—B(1)ix2.0913
FE(1)—FE(5B)xii2.4996FE(1B)—B(1)xvi2.0913
FE(1)—FE(5B)xiii2.4996FE(1B)—B(1)xvii2.0913
FE(1)—FE(5B)xiv2.4996FE(1B)—B(1)xviii2.0913
FE(1)—FE(5B)xv2.4996FE(1B)—B(1)xix2.0913
FE(1)—B(1)2.0913FE(1B)—B(1)x2.0913
FE(1)—B(1)ix2.0913FE(1B)—B(1)xi2.0913
FE(1)—B(1)xvi2.0913FE(2B)—FE(6B)2.4950
FE(1)—B(1)xvii2.0913FE(2B)—FE(6B)xx2.4950
FE(1)—B(1)xviii2.0913FE(2B)—FE(6B)xxi2.4950
FE(1)—B(1)xix2.0913FE(2B)—FE(6B)xix2.4950
FE(1)—B(1)x2.0913FE(3B)—FE(3B)ix2.4432
FE(1)—B(1)xi2.0913FE(3B)—FE(3B)x2.4432
FE(2)—FE(6)2.4950FE(3B)—FE(6B)xii2.3979
FE(2)—FE(6)xx2.4950FE(3B)—FE(6B)xiv2.3979
FE(2)—FE(6)xxi2.4950FE(5B)—FE(6B)xxii2.4653
FE(2)—FE(6)xix2.4950FE(5B)—B(1)xxiv2.1093
FE(2)—FE(6B)2.4950FE(5B)—B(1)xxii2.1093
FE(2)—FE(6B)xx2.4950FE(5B)—B(1)xxiii2.1093
FE(2)—FE(6B)xxi2.4950FE(5B)—B(1)xxv2.1093
FE(4)v—ND(2)—FE(4)vi157.6854FE(5)xii—FE(1B)—B(1)x53.8167
FE(4)v—ND(2)—FE(4)vii157.6854FE(5)xii—FE(1B)—B(1)xi132.0495
FE(4)v—ND(2)—FE(4B)vi157.6854FE(5)xiii—FE(1B)—FE(5)xiv117.0957
FE(4)v—ND(2)—FE(4B)vii157.6854FE(5)xiii—FE(1B)—FE(5)xv62.4570
FE(4)vi—ND(2)—FE(4)viii157.6854FE(5)xiii—FE(1B)—FE(3B)62.2400
FE(4)vi—ND(2)—FE(4B)v157.6854FE(5)xiii—FE(1B)—FE(3B)ix111.2731
FE(4)vi—ND(2)—FE(4B)viii157.6854FE(5)xiii—FE(1B)—FE(3B)x111.2731
FE(4)vii—ND(2)—FE(4)viii157.6854FE(5)xiii—FE(1B)—FE(3B)xi62.2400
FE(4)vii—ND(2)—FE(4B)v157.6854FE(5)xiii—FE(1B)—FE(5B)xii173.2478
FE(4)vii—ND(2)—FE(4B)viii157.6854FE(5)xiii—FE(1B)—FE(5B)xiv117.0957
FE(4)viii—ND(2)—FE(4B)vi157.6854FE(5)xiii—FE(1B)—FE(5B)xv62.4570
FE(4)viii—ND(2)—FE(4B)vii157.6854FE(5)xiii—FE(1B)—B(1)53.8167
FE(4B)v—ND(2)—FE(4B)vi157.6854FE(5)xiii—FE(1B)—B(1)ix132.0495
FE(4B)v—ND(2)—FE(4B)vii157.6854FE(5)xiii—FE(1B)—B(1)xvi53.8167
FE(4B)vi—ND(2)—FE(4B)viii157.6854FE(5)xiii—FE(1B)—B(1)xvii132.0495
FE(4B)vii—ND(2)—FE(4B)viii157.6854FE(5)xiii—FE(1B)—B(1)xviii132.0495
FE(4)v—ND(2B)—FE(4)vi157.6854FE(5)xiii—FE(1B)—B(1)xix53.8167
FE(4)v—ND(2B)—FE(4)vii157.6854FE(5)xiii—FE(1B)—B(1)x132.0495
FE(4)v—ND(2B)—FE(4B)vi157.6854FE(5)xiii—FE(1B)—B(1)xi53.8167
FE(4)v—ND(2B)—FE(4B)vii157.6854FE(5)xiv—FE(1B)—FE(5)xv173.2478
FE(4)vi—ND(2B)—FE(4)viii157.6854FE(5)xiv—FE(1B)—FE(3B)111.2730
FE(4)vi—ND(2B)—FE(4B)v157.6854FE(5)xiv—FE(1B)—FE(3B)ix62.2399
FE(4)vi—ND(2B)—FE(4B)viii157.6854FE(5)xiv—FE(1B)—FE(3B)x62.2399
FE(4)vii—ND(2B)—FE(4)viii157.6854FE(5)xiv—FE(1B)—FE(3B)xi111.2730
FE(4)vii—ND(2B)—FE(4B)v157.6854FE(5)xiv—FE(1B)—FE(5B)xii62.4570
FE(4)vii—ND(2B)—FE(4B)viii157.6854FE(5)xiv—FE(1B)—FE(5B)xiii117.0957
FE(4)viii—ND(2B)—FE(4B)vi157.6854FE(5)xiv—FE(1B)—FE(5B)xv173.2478
FE(4)viii—ND(2B)—FE(4B)vii157.6854FE(5)xiv—FE(1B)—B(1)132.0495
FE(4B)v—ND(2B)—FE(4B)vi157.6854FE(5)xiv—FE(1B)—B(1)ix53.8167
FE(4B)v—ND(2B)—FE(4B)vii157.6854FE(5)xiv—FE(1B)—B(1)xvi132.0495
FE(4B)vi—ND(2B)—FE(4B)viii157.6854FE(5)xiv—FE(1B)—B(1)xvii53.8167
FE(4B)vii—ND(2B)—FE(4B)viii157.6854FE(5)xiv—FE(1B)—B(1)xviii53.8167
FE(3)—FE(1)—FE(3)ix58.1093FE(5)xiv—FE(1B)—B(1)xix132.0495
FE(3)—FE(1)—FE(3)x58.1093FE(5)xiv—FE(1B)—B(1)x53.8167
FE(3)—FE(1)—FE(5)xii111.2730FE(5)xiv—FE(1B)—B(1)xi132.0495
FE(3)—FE(1)—FE(5)xiii62.2400FE(5)xv—FE(1B)—FE(3B)62.2400
FE(3)—FE(1)—FE(5)xiv111.2730FE(5)xv—FE(1B)—FE(3B)ix111.2731
FE(3)—FE(1)—FE(5)xv62.2400FE(5)xv—FE(1B)—FE(3B)x111.2731
FE(3)—FE(1)—FE(3B)ix58.1093FE(5)xv—FE(1B)—FE(3B)xi62.2400
FE(3)—FE(1)—FE(3B)x58.1093FE(5)xv—FE(1B)—FE(5B)xii117.0957
FE(3)—FE(1)—FE(5B)xii111.2730FE(5)xv—FE(1B)—FE(5B)xiii62.4570
FE(3)—FE(1)—FE(5B)xiii62.2400FE(5)xv—FE(1B)—FE(5B)xiv173.2478
FE(3)—FE(1)—FE(5B)xiv111.2730FE(5)xv—FE(1B)—B(1)53.8167
FE(3)—FE(1)—FE(5B)xv62.2400FE(5)xv—FE(1B)—B(1)ix132.0495
FE(3)—FE(1)—B(1)103.3341FE(5)xv—FE(1B)—B(1)xvi53.8167
FE(3)—FE(1)—B(1)ix161.4434FE(5)xv—FE(1B)—B(1)xvii132.0495
FE(3)—FE(1)—B(1)xvi103.3341FE(5)xv—FE(1B)—B(1)xviii132.0495
FE(3)—FE(1)—B(1)xvii161.4434FE(5)xv—FE(1B)—B(1)xix53.8167
FE(3)—FE(1)—B(1)xviii161.4434FE(5)xv—FE(1B)—B(1)x132.0495
FE(3)—FE(1)—B(1)xix103.3341FE(5)xv—FE(1B)—B(1)xi53.8167
FE(3)—FE(1)—B(1)x161.4434FE(3B)—FE(1B)—FE(3B)ix58.1093
FE(3)—FE(1)—B(1)xi103.3341FE(3B)—FE(1B)—FE(3B)x58.1093
FE(3)ix—FE(1)—FE(3)xi58.1093FE(3B)—FE(1B)—FE(5B)xii111.2730
FE(3)ix—FE(1)—FE(5)xii62.2399FE(3B)—FE(1B)—FE(5B)xiii62.2400
FE(3)ix—FE(1)—FE(5)xiii111.2731FE(3B)—FE(1B)—FE(5B)xiv111.2730
FE(3)ix—FE(1)—FE(5)xiv62.2399FE(3B)—FE(1B)—FE(5B)xv62.2400
FE(3)ix—FE(1)—FE(5)xv111.2731FE(3B)—FE(1B)—B(1)103.3341
FE(3)ix—FE(1)—FE(3B)58.1093FE(3B)—FE(1B)—B(1)ix161.4434
FE(3)ix—FE(1)—FE(3B)xi58.1093FE(3B)—FE(1B)—B(1)xvi103.3341
FE(3)ix—FE(1)—FE(5B)xii62.2399FE(3B)—FE(1B)—B(1)xvii161.4434
FE(3)ix—FE(1)—FE(5B)xiii111.2731FE(3B)—FE(1B)—B(1)xviii161.4434
FE(3)ix—FE(1)—FE(5B)xiv62.2399FE(3B)—FE(1B)—B(1)xix103.3341
FE(3)ix—FE(1)—FE(5B)xv111.2731FE(3B)—FE(1B)—B(1)x161.4434
FE(3)ix—FE(1)—B(1)161.4434FE(3B)—FE(1B)—B(1)xi103.3341
FE(3)ix—FE(1)—B(1)ix103.3341FE(3B)ix—FE(1B)—FE(3B)xi58.1093
FE(3)ix—FE(1)—B(1)xvi161.4434FE(3B)ix—FE(1B)—FE(5B)xii62.2399
FE(3)ix—FE(1)—B(1)xvii103.3341FE(3B)ix—FE(1B)—FE(5B)xiii111.2731
FE(3)ix—FE(1)—B(1)xviii103.3341FE(3B)ix—FE(1B)—FE(5B)xiv62.2399
FE(3)ix—FE(1)—B(1)xix161.4434FE(3B)ix—FE(1B)—FE(5B)xv111.2731
FE(3)ix—FE(1)—B(1)x103.3341FE(3B)ix—FE(1B)—B(1)161.4434
FE(3)ix—FE(1)—B(1)xi161.4434FE(3B)ix—FE(1B)—B(1)ix103.3341
FE(3)x—FE(1)—FE(3)xi58.1093FE(3B)ix—FE(1B)—B(1)xvi161.4434
FE(3)x—FE(1)—FE(5)xii62.2399FE(3B)ix—FE(1B)—B(1)xvii103.3341
FE(3)x—FE(1)—FE(5)xiii111.2731FE(3B)ix—FE(1B)—B(1)xviii103.3341
FE(3)x—FE(1)—FE(5)xiv62.2399FE(3B)ix—FE(1B)—B(1)xix161.4434
FE(3)x—FE(1)—FE(5)xv111.2731FE(3B)ix—FE(1B)—B(1)x103.3341
FE(3)x—FE(1)—FE(3B)58.1093FE(3B)ix—FE(1B)—B(1)xi161.4434
FE(3)x—FE(1)—FE(3B)xi58.1093FE(3B)x—FE(1B)—FE(3B)xi58.1093
FE(3)x—FE(1)—FE(5B)xii62.2399FE(3B)x—FE(1B)—FE(5B)xii62.2399
FE(3)x—FE(1)—FE(5B)xiii111.2731FE(3B)x—FE(1B)—FE(5B)xiii111.2731
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Symmetry codes: (i) x+1, y+1, z; (ii) y+1, x+1, z; (iii) x+1, y+1, z; (iv) y+1, x+1, z; (v) y+1/2, x+1/2, z1/2; (vi) x+1/2, y+1/2, z+1/2; (vii) y+1/2, x+1/2, z+1/2; (viii) x+1/2, y+1/2, z1/2; (ix) x, y, z; (x) y, x, z; (xi) y, x, z; (xii) x+1/2, y1/2, z+1/2; (xiii) x1/2, y+1/2, z+1/2; (xiv) y1/2, x+1/2, z+1/2; (xv) y+1/2, x1/2, z+1/2; (xvi) y, x, z; (xvii) y, x, z; (xviii) x, y, z; (xix) x, y, z; (xx) x, y+1, z; (xxi) x, y+1, z; (xxii) x+1/2, y+1/2, z+1/2; (xxiii) y+1/2, x+1/2, z+1/2; (xxiv) y+1/2, x+1/2, z+1/2; (xxv) x+1/2, y+1/2, z+1/2; (xxvi) y+1/2, x1/2, z1/2; (xxvii) x1/2, y+1/2, z1/2.
 

Acknowledgements

The synchrotron experiments were performed at SPring-8 BL02B1 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (proposal Nos. 2018b0078, 2019a0159 and 2021a1744).

Funding information

The work was supported by the Villum Foundation (grant No. 25861) and the Danish National Research Foundation (grant No. DNRF189). This work was partly supported by the Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research (KAKENHI) (grant Nos. JP19KK0132, JP20H4656 and JP2105235).

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Volume 12| Part 6| November 2025| Pages 658-669
ISSN: 2052-2525