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metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 64| Part 8| August 2008| Pages m984-m985
doi:10.1107/S1600536808019296

Tris(ethanol-κO)tris­­(picrato-κ2O1,O2)lanthanum(III) tri-2-pyridylamine solvate

Eric J. Chana*

aResearch School of Chemistry, Building 35, Australian National University, Canberra, ACT 0200, Australia
*Correspondence e-mail: echanj@rsc.anu.edu.au

(Received 4 June 2008; accepted 25 June 2008; online 5 July 2008)

The title compound, [La(C6H2N3O7)3(C2H6O)3]·C15H12N4, has two mol­ecular building blocks, namely the neutral mononuclear adduct of lanthanum picrate with ethanol [i.e. La(pic)3:EtOH (1:3); La(pic)3 = lanthanum picrate and EtOH = ethanol] and the oligodentate aromatic nitro­gen base tri-2-pyridylamine (tpa). The asymmetric unit contains two formula units. The compound was prepared during an investigation of the stereochemistry of lanthanoid picrate complexes with O-donor ligands. The metal–ligand adduct adopts a nine-coordinate tricapped trigonal-prismatic metal atom environment. The stereochemical arrangement of the ligands about the metal core is typical of a fac-isomer with stoichiometry M(bidentate)3(monodentate)3. Face-to-face hydrogen bonds are found between the tpa mol­ecule and the ethanol ligands. One ethanol ligand is disordered over two positions, with site occupancy factors of ca 0.7 and 0.3. The oxygen atoms of a nitro group are also disordered over two positions; the site occupancy factors are ca 0.6 and 0.4.

Related literature

The compounds Ln(NO3)3(EtOH)3·tpa display identical structural features and are produced by a similar method of synthesis (Nagao et al., 2004[Nagao, N., Egashira, K. & Mogi, D. (2004). Bull. Chem. Soc. Jpn, 77, 1171-1172.]). For the stereochemistry of compounds with stoichiometry Ln(pic)3(unidentate)3 (pic = picrate), see: Chan (2006[Chan, E. J. (2006). Doctoral Thesis, School of Biomedical and Chemical Sciences, UWA, Australia.]). For an inter­pretation of the inter­molecular inter­actions between metal complexes with picrate ligands, see: Harrowfield (1996[Harrowfield, J. (1996). J. Chem. Soc. Dalton Trans. pp. 3165-3171.]). For the preparation of lanthanoid picrate hydrates, see: Harrowfield et al. (1994[Harrowfield, J. M., Skelton, B. W. & White, A. H. (1994). Aust. J. Chem. 47, 359-364.]). For the preferred stereochemical arrangement of multidentate ligands encompassing a nine-coordinate metal atom environment, see: Kepert (1986[Kepert, D. L. (1986). Inorganic Stereochemistry. Berlin: Springer-Verlag.]).

[Scheme 1]

Experimental

Crystal data

  • [La(C6H2N3O7)3(C2H6O)3]·C15H12N4

  • Mr = 1209.69

  • Triclinic, [P \overline 1]

  • a = 15.7554 (19) Å

  • b = 16.4752 (14) Å

  • c = 20.427 (4) Å

  • α = 101.714 (11)°

  • β = 111.610 (14)°

  • γ = 90.676 (8)°

  • V = 4805.1 (13) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.99 mm−1

  • T = 100 (2) K

  • 0.50 × 0.18 × 0.03 mm
Data collection

  • Oxford Diffraction Xcalibur diffractometer

  • Absorption correction: multi-scan (CrysAlis RED; Oxford Diffraction, 2006[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Abingdon, Oxfordshire, England.]) Tmin = 0.773, Tmax = 0.970

  • 58832 measured reflections

  • 28469 independent reflections

  • 14209 reflections with I > 2σ(I)

  • Rint = 0.049
Refinement

  • R[F2 > 2σ(F2)] = 0.043

  • wR(F2) = 0.086

  • S = 0.84

  • 28469 reflections

  • 1419 parameters

  • 104 restraints

  • H-atom parameters constrained

  • Δρmax = 2.85 e Å−3

  • Δρmin = −0.75 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
O011—H011⋯N111 0.84 1.90 2.740 (4) 175
O021—H021⋯N121 0.84 1.92 2.747 (3) 170
O031—H031⋯N131 0.84 1.90 2.693 (3) 158
O041—H041⋯N241i 0.84 1.88 2.721 (4) 179
O051—H051⋯N251i 0.84 1.93 2.769 (3) 172
O061—H061⋯N261i 0.84 1.85 2.692 (4) 175
Symmetry code: (i) x, y+1, z.

Data collection: CrysAlis CCD (Oxford Diffraction, 2006[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Abingdon, Oxfordshire, England.]); cell refinement: CrysAlis RED (Oxford Diffraction, 2006[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Abingdon, Oxfordshire, England.]); data reduction: CrysAlis RED; program(s) used to solve structure: SIR92 (Altomare et al., 1994[Altomare, A., Cascarano, G., Giacovazzo, C., Guagliardi, A., Burla, M. C., Polidori, G. & Camalli, M. (1994). J. Appl. Cryst. 27, 435.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: Xtal3.7 (Hall et al., 2001[Hall, S. R., du Boulay, D. J. & Olthof-Hazekamp, R. (2001). The Xtal3.7 System. The University of Western Australia, Australia.]); software used to prepare material for publication: Xtal3.7.

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808019296/zl2121sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808019296/zl2121Isup2.hkl

checkCIF report


Comment top

The title compound crystallizes in space group P1 with two independent groups of (C6H2N3O7-O,O')3La(O-C2H6O)3. (C5H4N)3N, (I), in the asymmetric unit (Z=4). Each individual bimolecular cluster comprises the metal-ligand adduct La(pic)3(EtOH)3 hydrogen bonded to the aromatic nitrogen base molecule tpa through a "face to face" arrangement in which the pyridine nitrogen atoms of the tpa molecules act as hydrogen bond acceptors and the hydroxy groups of ethanol ligands act as hydrogen bond donors (see Fig. 1 and Fig. 3). The primary coordination sphere of lanthanum is nine-coordinate, consisting only of ligand oxygen donor atoms, adopting the "fac" isomeric form of a tri-capped trigonal prism in which all three unidentate ethanol ligands occupy mutually "cis"-sites of one triangular face and the bidentate O,O'–picrate anions chelating through the phenoxy oxygen atoms at sites of the opposite triangular face and with an adjacent O–nitro oxygen atom at the capping site of each rectangular face (see Fig. 2).

The bimolecular cluster has a pseudo-threefold axis normal to the triangular faces of the tri-capped trigonal prism disposed about the lanthanum core. There is an obtuse (greater than 120°) nitro–O—La—O–nitro angle (approx. 125°) when compared with other angles associated with picrate nitro group oxygen atoms at the capping sites of the tri-capped trigonal prism (see Fig. 2, values for O121—La1—O321, O221 being 116.62 (7), 125.17 (7)° respectively with O321—La1—O221 being 117.88 (7)° and values for O421—La2—O621, O521 being 115.75 (7), 126.73 (7)° respectively with O621—La2—O521 being 117.28 (7)°). Presumably, the length of the corresponding rectangular edge (phenoxide oxygen and ethanol oxygen donor atoms) of the trigonal prism opposite to this angle becomes the shortest rectangular edge distance as a result of minimizing strain (contact distances for O11···O011, O21···O021 and O31···O031 being 3.217 (3), 3.341 (3) and 3.400 (4) Å respectively, with contact distances for O41···O041, O51···O051 and O61···O061 being 3.115 (4), 3.397 (4) and 3.483 (4) Å respectively). This observation exists concomitantly with a distortion of the inter-planar dihedral angle between the tpa pyridyl group, whose nitrogen atom is hydrogen bonded to the ethanol ligand which is associated with the above mentioned shorter rectangular edge, and the central NC3 plane of the tpa molecule. Noticeably, the dihedral angles between the NC3 and C5N planes of tpa which comprise nitrogen atoms labelled N111, N121 and N131 are 44.7 (1), 39.0 (1) and 40.0 (1)° respectively. The corresponding dihedral angles found in the second set of molecular coordinates for planes comprising nitrogen atoms N241, N251 and N261 are 45.7 (1), 40.6 (1) and 37.4 (1)° respectively. In agreement with the previous statement the angles for N111 and N241 are seen to be significantly larger.

Related literature top

The compounds Ln(NO3)3(EtOH)3.tpa display identical structural features and are produced by a similar method of synthesis (Nagao et al., 2004). For the stereochemistry of compounds with stoichiometry Ln(pic)3(unidentate)3 (pic = picrate), see: Chan (2006). For an interpretation of the intermolecular interactions between metal complexes with picrate ligands, see: Harrowfield (1996). For the preparation of lanthanoid picrate hydrates, see: Harrowfield et al. (1994). For the preferred stereochemical arrangement of multidentate ligands encompassing a nine-coordinate metal atom environment, see: Kepert (1986).

Experimental top

Using a 1:1 mole ratio, hydrated La(pic)3 (Harrowfield et al.,, 1994) and tpa was dissolved in a suitable volume of 70% v/v ethanol in triethyl orthoformate (used in the synthesis as a dehydrating agent). The mixture was then heated under reflux for 1 h ensuring formation of complex is complete. The solution was then filtered while hot into a Shlenk tube fitted with vacuum and nitrogen outlet. The solvent was removed under vacuum until the contents were sufficiently concentrated, the product was then allowed to cool slowly until yellow crystals deposited.

Refinement top

All H atoms, with the exception of those associated with the hydroxy groups of the ethanol molecules, were positioned geometrically and refined using a riding model with C—H = 0.95–0.99 Å, and with Uiso(H) = 1.2 (1.5 for methyl groups) times Ueq(C). The hydroxy H atoms of the ethanol molecules were, in the early stages of refinement, built geometrically as idealized OH groups and refined using a riding model (allowing rotation about the C—O bond) until the mean shift/e.s.d. was at a minimum of 0.01, with the C—O—H angle tetrahedral and O—H = 0.80–0.85 Å, and with Uiso(H) = 1.5 times Ueq(O). A further five final cycles of refinement were performed with the hydroxy H atom positions fixed in order to allow hydroxy oxygen atom to lanthanum metal atom bond lengths with associated angles to be included in the connectivity list. Quasi-in-plane orientational disorder was exhibited for the totality of ethanol ligand "03" (with the exception of its La-bound oxygen atom "O031"). All 1,2– and 1,3– distances for the disordered atoms were restrained so that both fragments would have similar geometries (i.e. the SAME restraint, using the default 0.02 s.u. values). The sum of the site occupation parameters for both disordered groups was constrained to unity during refinement giving a major site occupation component value of 0.664 (8) with that of the minor component value complementary. All atoms of the disordered ethanol group closer than 1.7 Å were restrained to have similar Uij components (i.e. the SIMU restraint was applied) with the default 0.04 (central C atom) and 0.08 (terminal C and O atoms) s.u. values. The oxygen atoms of the "36" picrate nitro group exhibit rotational disorder around the N—C bond. During refinement the N—O distances were restrained to be the same (i.e. the SADI restraint, using the default 0.02 s.u. value) and atoms of each of the CNO2 fragments (atoms C36 and N36 both being a part of each planar group) were restrained to lie in a common plane (i.e. the FLAT restraint, using the default 0.1 s.u. value). The sum of site occupancies was constrained to unity, oxygen fragments refining to a major site occupation value of 0.58 (2) with a minor component value complementary. All atoms of the disordered nitro group closer than 1.7 Å were restrained to have similar Uij components (i.e. the SIMU restraint was applied) with the default 0.04 (central N atom) and 0.08 (terminal O atoms) s.u. values.

Computing details top

Data collection: CrysAlis CCD (Oxford Diffraction, 2006); cell refinement: CrysAlis RED (Oxford Diffraction, 2006); data reduction: CrysAlis RED (Oxford Diffraction, 2006); program(s) used to solve structure: SIR92 (Altomare et al., 1994); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: Xtal3.7 (Hall et al., 2001); software used to prepare material for publication: Xtal3.7 (Hall et al., 2001).

Figures top
[Figure 1] Fig. 1. View of the molecular structure of (I) depicting the tris(2-pyridyl)amine molecule interacting with the (C6H2N3O7-O,O')3(C2H6O-O)3La(III) adduct through O—H···N hydrogen bonds. 50% probability displacement ellipsoids are shown for non-H atoms. Enhanced figure is accessible at http://submission.iucr.org/jtkt/serve/z/u4xwab7OUyDKQ3um/zz0000/0/
[Figure 2] Fig. 2. Labelled ORTEP diagram of the tris(ethanol-O)tris(picrato-O,O')lanthanum(III) neutral mononuclear adduct projected through the triangular faces of its 9-coordinate tri-capped trigonal prismatic metal environment. 50% probability displacement ellipsoids are shown for non-H atoms.
[Figure 3] Fig. 3. Packing diagram of (I) viewed down the c-axis. The O—H···N hydrogen bonds are shown as dotted lines. 50% probability displacement ellipsoids are shown for non-H atoms.
Tris(ethanol-κO)tris(picrato-κ2O1,O2)lanthanum(III) tri-2-pyridylamine solvate top
Crystal data top
[La(C6H2N3O7)3(C2H6O)3]·C15H12N4Z = 4
Mr = 1209.69F(000) = 2440
Triclinic, P1Dx = 1.672 Mg m−3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 15.7554 (19) ÅCell parameters from 16526 reflections
b = 16.4752 (14) Åθ = 2.6–31.2°
c = 20.427 (4) ŵ = 0.99 mm−1
α = 101.714 (11)°T = 100 K
β = 111.610 (14)°Plate, yellow
γ = 90.676 (8)°0.50 × 0.18 × 0.03 mm
V = 4805.1 (13) Å3
Data collection top
Oxford Diffraction Xcalibur
diffractometer		28469 independent reflections
Radiation source: fine-focus sealed tube14209 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.049
Detector resolution: 16.0009 pixels mm-1θmax = 31.2°, θmin = 2.6°
ω scansh = −22→22
Absorption correction: multi-scan
(CrysAlis RED; Oxford Diffraction, 2006)		k = −23→23
Tmin = 0.773, Tmax = 0.970l = −29→29
58832 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.043Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.086H-atom parameters constrained
S = 0.84 w = 1/[σ2(Fo2) + (0.031P)2]
where P = (Fo2 + 2Fc2)/3
28469 reflections(Δ/σ)max = 0.047
1419 parametersΔρmax = 2.85 e Å−3
104 restraintsΔρmin = −0.75 e Å−3
Crystal data top
[La(C6H2N3O7)3(C2H6O)3]·C15H12N4γ = 90.676 (8)°
Mr = 1209.69V = 4805.1 (13) Å3
Triclinic, P1Z = 4
a = 15.7554 (19) ÅMo Kα radiation
b = 16.4752 (14) ŵ = 0.99 mm−1
c = 20.427 (4) ÅT = 100 K
α = 101.714 (11)°0.50 × 0.18 × 0.03 mm
β = 111.610 (14)°
Data collection top
Oxford Diffraction Xcalibur
diffractometer		28469 independent reflections
Absorption correction: multi-scan
(CrysAlis RED; Oxford Diffraction, 2006)		14209 reflections with I > 2σ(I)
Tmin = 0.773, Tmax = 0.970Rint = 0.049
58832 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.043104 restraints
wR(F2) = 0.086H-atom parameters constrained
S = 0.84Δρmax = 2.85 e Å−3
28469 reflectionsΔρmin = −0.75 e Å−3
1419 parameters
Special details top

Experimental. CrysAlis RED (Oxford Diffraction, 2006) Empirical absorption correction using spherical harmonics as implemented in the SCALE3 ABSPACK scaling algorithm.

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

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
La10.860784 (13)0.552421 (12)0.752304 (10)0.01733 (5)
O110.84562 (14)0.40793 (13)0.69097 (11)0.0192 (5)
C110.8443 (2)0.33456 (19)0.70167 (17)0.0162 (7)
C120.8586 (2)0.31263 (19)0.76897 (18)0.0192 (7)
C130.8654 (2)0.2323 (2)0.7780 (2)0.0231 (8)
H130.88040.22130.82470.028*
C140.8503 (2)0.16812 (19)0.71953 (19)0.0203 (7)
C150.8328 (2)0.1827 (2)0.65141 (19)0.0211 (8)
H150.82320.13790.61120.025*
C160.8296 (2)0.2627 (2)0.64365 (18)0.0193 (7)
N120.86660 (19)0.37655 (18)0.83211 (16)0.0244 (7)
O1210.83658 (16)0.44447 (14)0.82365 (12)0.0256 (5)
O1220.89884 (19)0.36014 (15)0.89202 (13)0.0386 (7)
N140.84826 (19)0.08238 (18)0.7297 (2)0.0295 (8)
O1410.87984 (16)0.06817 (16)0.78795 (16)0.0373 (7)
O1420.81122 (16)0.02741 (14)0.67350 (14)0.0303 (6)
N160.8119 (2)0.27897 (17)0.57155 (15)0.0238 (7)
O1610.75047 (17)0.32233 (15)0.54706 (13)0.0333 (6)
O1620.86114 (17)0.24768 (15)0.54005 (13)0.0340 (6)
O210.95890 (14)0.55337 (14)0.68478 (12)0.0227 (5)
C210.9606 (2)0.5047 (2)0.62887 (19)0.0234 (8)
C220.8859 (2)0.4847 (2)0.56022 (18)0.0221 (8)
C230.8899 (3)0.4340 (2)0.49848 (19)0.0286 (9)
H230.83920.42520.45360.034*
C240.9694 (3)0.3969 (2)0.5041 (2)0.0294 (9)
C251.0435 (3)0.4080 (2)0.5692 (2)0.0317 (9)
H251.09630.37930.57280.038*
C261.0389 (2)0.4614 (2)0.6284 (2)0.0246 (8)
N220.7984 (2)0.51949 (17)0.55199 (17)0.0259 (7)
O2210.77665 (15)0.53675 (14)0.60512 (12)0.0256 (6)
O2220.74856 (18)0.52775 (17)0.49225 (14)0.0414 (7)
N240.9739 (3)0.3425 (2)0.4392 (2)0.0439 (10)
O2410.9067 (2)0.33343 (19)0.38276 (18)0.0616 (10)
O2421.0466 (2)0.31122 (18)0.44525 (17)0.0598 (9)
N261.1194 (2)0.4714 (2)0.69646 (18)0.0330 (8)
O2611.14614 (16)0.54218 (16)0.73386 (14)0.0362 (7)
O2621.15419 (18)0.40807 (18)0.71157 (16)0.0479 (8)
O311.00390 (15)0.51721 (13)0.83415 (12)0.0236 (5)
C311.0896 (2)0.5396 (2)0.86261 (18)0.0206 (8)
C321.1283 (2)0.62516 (19)0.88504 (17)0.0170 (7)
C331.2209 (2)0.6484 (2)0.92038 (17)0.0213 (8)
H331.24340.70560.93480.026*
C341.2801 (2)0.5889 (2)0.93453 (19)0.0242 (8)
C351.2499 (2)0.5048 (2)0.91411 (19)0.0261 (8)
H351.29220.46410.92470.031*
C361.1579 (2)0.48161 (19)0.87832 (19)0.0248 (8)
N321.0704 (2)0.69303 (17)0.86917 (15)0.0219 (6)
O3210.98921 (15)0.67753 (13)0.82651 (13)0.0247 (5)
O3221.10475 (15)0.76525 (14)0.89742 (13)0.0278 (6)
N341.37835 (19)0.61448 (19)0.97202 (16)0.0254 (7)
O3411.40413 (15)0.68896 (15)0.99330 (13)0.0298 (6)
O3421.43025 (16)0.55841 (15)0.98042 (14)0.0350 (6)
N361.1311 (2)0.39154 (18)0.85566 (18)0.0359 (8)
O3611.0590 (7)0.3646 (14)0.8045 (8)0.039 (3)0.59 (2)
O3621.1776 (6)0.3455 (4)0.8937 (7)0.048 (3)0.59 (2)
O3631.0508 (9)0.366 (2)0.8229 (11)0.039 (3)0.41 (2)
O3641.1983 (6)0.3466 (5)0.8618 (9)0.034 (4)0.41 (2)
O0110.69116 (14)0.52258 (13)0.71509 (12)0.0237 (5)
H0110.66450.54500.74190.036*
C0110.6261 (2)0.4638 (2)0.65326 (19)0.0256 (8)
H01A0.65660.44060.61990.031*
H01B0.57450.49340.62700.031*
C0120.5896 (3)0.3944 (3)0.6747 (2)0.0548 (13)
H01C0.54630.35630.63150.082*
H01D0.55800.41690.70680.082*
H01E0.64030.36430.70000.082*
O0210.81139 (14)0.68541 (13)0.71535 (12)0.0208 (5)
H0210.75540.69280.70010.031*
C0210.8602 (2)0.7417 (2)0.69256 (19)0.0235 (8)
H02A0.91500.71640.68790.028*
H02B0.88140.79420.72990.028*
C0220.8015 (2)0.7608 (2)0.6218 (2)0.0332 (9)
H02C0.83720.79860.60810.050*
H02D0.74810.78720.62650.050*
H02E0.78110.70900.58450.050*
O0310.83140 (16)0.62240 (13)0.86196 (12)0.0261 (6)0.661 (8)
H0310.80100.66320.85340.039*0.661 (8)
C0310.8293 (4)0.6018 (3)0.9284 (3)0.0241 (15)0.661 (8)
H03A0.79300.54770.91690.029*0.661 (8)
H03B0.80150.64530.95290.029*0.661 (8)
C0320.9264 (4)0.5973 (4)0.9753 (3)0.0297 (17)0.661 (8)
H03C0.92880.58411.02060.044*0.661 (8)
H03D0.96140.65110.98580.044*0.661 (8)
H03E0.95280.55390.95040.044*0.661 (8)
O0330.83140 (16)0.62240 (13)0.86196 (12)0.0261 (6)0.339 (8)
H0330.81230.66980.86280.039*0.339 (8)
C0330.9030 (7)0.6198 (7)0.9377 (5)0.023 (3)0.339 (8)
H03F0.94750.57930.93310.028*0.339 (8)
H03G0.93690.67530.96230.028*0.339 (8)
C0340.8519 (7)0.5942 (8)0.9799 (6)0.039 (4)0.339 (8)
H03H0.89520.59261.02840.058*0.339 (8)
H03I0.81930.53890.95540.058*0.339 (8)
H03J0.80770.63440.98370.058*0.339 (8)
N1000.63018 (17)0.71629 (16)0.77801 (14)0.0186 (6)
N1110.60883 (17)0.59039 (17)0.80784 (15)0.0206 (6)
C1120.5936 (2)0.5476 (2)0.85276 (19)0.0249 (8)
H1120.58830.48840.83970.030*
C1130.5853 (2)0.5851 (2)0.91656 (19)0.0240 (8)
H1130.57340.55260.94620.029*
C1140.5945 (2)0.6707 (2)0.93635 (19)0.0256 (8)
H1140.59030.69820.98050.031*
C1150.6101 (2)0.7161 (2)0.89125 (18)0.0244 (8)
H1150.61600.77530.90340.029*
C1160.6169 (2)0.6733 (2)0.82803 (17)0.0178 (7)
N1210.62439 (18)0.68932 (16)0.65925 (15)0.0220 (6)
C1220.5771 (2)0.6647 (2)0.58794 (19)0.0248 (8)
H1220.60830.66780.55650.030*
C1230.4864 (2)0.6354 (2)0.5580 (2)0.0296 (9)
H1230.45600.61690.50710.035*
C1240.4395 (2)0.6333 (2)0.6038 (2)0.0277 (8)
H1240.37650.61320.58470.033*
C1250.4861 (2)0.6609 (2)0.67723 (19)0.0227 (8)
H1250.45560.66100.70960.027*
C1260.5789 (2)0.68842 (19)0.70310 (17)0.0184 (7)
N1310.77762 (18)0.77605 (16)0.85513 (14)0.0206 (6)
C1320.8455 (2)0.8387 (2)0.87808 (19)0.0254 (8)
H1320.90140.83480.91620.030*
C1330.8375 (2)0.9074 (2)0.84895 (18)0.0241 (8)
H1330.88740.94910.86510.029*
C1340.7552 (2)0.9146 (2)0.79552 (19)0.0259 (8)
H1340.74770.96200.77480.031*
C1350.6838 (2)0.8532 (2)0.77220 (18)0.0226 (8)
H1350.62630.85750.73600.027*
C1360.6987 (2)0.78497 (19)0.80338 (17)0.0178 (7)
La20.633752 (13)0.916258 (12)0.243353 (10)0.01671 (5)
O410.64846 (14)0.80202 (14)0.30240 (11)0.0198 (5)
C410.6527 (2)0.7237 (2)0.29249 (18)0.0219 (8)
C420.6402 (2)0.66825 (19)0.22517 (17)0.0172 (7)
C430.6363 (2)0.5827 (2)0.21597 (19)0.0207 (7)
H430.62370.54800.16960.025*
C440.6511 (2)0.5485 (2)0.27501 (19)0.0207 (7)
C450.6658 (2)0.5979 (2)0.34318 (18)0.0219 (8)
H450.67430.57360.38320.026*
C460.6676 (2)0.6820 (2)0.35048 (17)0.0175 (7)
N420.63182 (18)0.69970 (17)0.16134 (15)0.0206 (6)
O4210.65665 (15)0.77426 (13)0.16916 (12)0.0226 (5)
O4220.60455 (17)0.65152 (15)0.10237 (13)0.0335 (6)
N440.65393 (18)0.45574 (17)0.26500 (17)0.0196 (6)
O4410.62705 (16)0.41551 (15)0.20558 (16)0.0340 (7)
O4420.68841 (16)0.43226 (14)0.32138 (14)0.0306 (6)
N460.6819 (2)0.73521 (18)0.42171 (16)0.0262 (7)
O4610.74305 (17)0.79230 (15)0.44626 (13)0.0338 (6)
O4620.63206 (17)0.71809 (16)0.45197 (13)0.0366 (6)
O510.53601 (14)0.94981 (13)0.31108 (12)0.0215 (5)
C510.5352 (2)0.93254 (19)0.36869 (18)0.0184 (7)
C520.6101 (2)0.9501 (2)0.43716 (18)0.0219 (8)
C530.6056 (2)0.9327 (2)0.49947 (18)0.0249 (8)
H530.65650.94790.54410.030*
C540.5259 (3)0.8932 (2)0.49544 (19)0.0263 (8)
C550.4513 (2)0.8701 (2)0.4309 (2)0.0265 (8)
H550.39770.84060.42850.032*
C560.4557 (2)0.8906 (2)0.37010 (19)0.0229 (8)
N520.6967 (2)0.98864 (17)0.44359 (17)0.0251 (7)
O5210.71871 (14)0.97801 (14)0.39039 (12)0.0234 (5)
O5220.74768 (17)1.02960 (15)0.50342 (14)0.0354 (6)
N540.5208 (3)0.8752 (2)0.56113 (19)0.0368 (8)
O5410.5884 (2)0.89389 (19)0.61692 (15)0.0522 (8)
O5420.4460 (2)0.84492 (18)0.55689 (15)0.0500 (8)
N560.37638 (19)0.8642 (2)0.30236 (16)0.0283 (7)
O5610.34683 (16)0.91519 (16)0.26496 (13)0.0335 (6)
O5620.34174 (17)0.79208 (17)0.28666 (15)0.0445 (7)
O610.49117 (14)0.83816 (13)0.15971 (12)0.0204 (5)
C610.4058 (2)0.8434 (2)0.13435 (17)0.0180 (7)
C620.3641 (2)0.9168 (2)0.11297 (18)0.0207 (8)
C630.2705 (2)0.9208 (2)0.08079 (17)0.0196 (7)
H630.24670.97010.06690.023*
C640.2121 (2)0.8507 (2)0.06938 (16)0.0174 (7)
C650.2457 (2)0.7779 (2)0.08790 (17)0.0191 (7)
H650.20500.73030.07890.023*
C660.3380 (2)0.7753 (2)0.11914 (18)0.0212 (7)
N620.42103 (18)0.99304 (16)0.12567 (15)0.0194 (6)
O6210.50192 (15)1.00287 (13)0.16861 (12)0.0230 (5)
O6220.38583 (15)1.04725 (14)0.09305 (13)0.0316 (6)
N640.11342 (18)0.85389 (18)0.03600 (15)0.0227 (7)
O6410.08434 (15)0.91680 (14)0.01608 (13)0.0265 (6)
O6420.06349 (15)0.79255 (15)0.03100 (13)0.0315 (6)
N660.3699 (2)0.69686 (18)0.13932 (17)0.0275 (7)
O6610.44218 (16)0.69852 (15)0.19101 (15)0.0351 (6)
O6620.32053 (17)0.63251 (15)0.10357 (15)0.0397 (7)
O0410.80292 (14)0.90418 (13)0.28443 (11)0.0210 (5)
H0410.82970.91080.25690.031*
C0410.8663 (2)0.8781 (2)0.34645 (19)0.0250 (8)
H04A0.83380.86810.37770.030*
H04B0.91600.92340.37480.030*
C0420.9081 (3)0.7998 (2)0.3252 (2)0.0490 (12)
H04C0.94980.78400.36880.073*
H04D0.94220.81010.29570.073*
H04E0.85920.75470.29740.073*
O0510.68822 (14)1.06876 (12)0.27962 (12)0.0190 (5)
H0510.74501.08270.29830.028*
C0510.6404 (2)1.13673 (19)0.30115 (18)0.0215 (8)
H05A0.58461.11410.30530.026*
H05B0.62101.16970.26350.026*
C0520.6994 (2)1.1925 (2)0.37188 (19)0.0288 (9)
H05C0.66481.23780.38480.043*
H05D0.75421.21580.36760.043*
H05E0.71781.16030.40950.043*
O0610.67246 (14)0.93827 (13)0.13884 (12)0.0204 (5)
H0610.69200.98750.14310.031*
C0610.6547 (2)0.8914 (2)0.06678 (17)0.0217 (8)
H06A0.67910.83650.06890.026*
H06B0.68640.92140.04360.026*
C0620.5527 (2)0.8792 (2)0.02221 (19)0.0268 (8)
H06C0.54170.8463−0.02640.040*
H06D0.52900.93350.01890.040*
H06E0.52140.84970.04530.040*
N2000.87961 (17)0.07030 (16)0.22678 (14)0.0190 (6)
N2410.88834 (17)−0.07251 (16)0.19476 (15)0.0186 (6)
C2420.8960 (2)−0.1403 (2)0.14801 (19)0.0231 (8)
H2420.8947−0.19320.15960.028*
C2430.9055 (2)−0.1362 (2)0.08426 (19)0.0244 (8)
H2430.9108−0.18490.05250.029*
C2440.9072 (2)−0.0592 (2)0.06807 (18)0.0230 (8)
H2440.9137−0.05440.02450.028*
C2450.8995 (2)0.0114 (2)0.11468 (17)0.0199 (7)
H2450.90070.06480.10420.024*
C2460.8900 (2)0.0010 (2)0.17702 (18)0.0194 (7)
N2510.87729 (18)0.09980 (16)0.34369 (15)0.0215 (6)
C2520.9208 (2)0.1091 (2)0.41534 (18)0.0233 (8)
H2520.88720.12560.44530.028*
C2531.0108 (2)0.0960 (2)0.44737 (19)0.0292 (9)
H2531.03910.10360.49830.035*
C2541.0599 (2)0.0713 (2)0.40365 (19)0.0280 (8)
H2541.12200.05990.42430.034*
C2551.0178 (2)0.0635 (2)0.33003 (18)0.0233 (8)
H2551.05040.04860.29910.028*
C2560.9253 (2)0.07830 (19)0.30257 (18)0.0189 (7)
N2610.73700 (17)0.09295 (16)0.14540 (14)0.0188 (6)
C2620.6732 (2)0.1446 (2)0.12181 (19)0.0255 (8)
H2620.61950.12230.08050.031*
C2630.6803 (2)0.2279 (2)0.15349 (19)0.0279 (8)
H2630.63180.26130.13630.033*
C2640.7607 (2)0.2612 (2)0.21132 (19)0.0242 (8)
H2640.76850.31850.23450.029*
C2650.8291 (2)0.21070 (19)0.23486 (17)0.0200 (7)
H2650.88560.23280.27320.024*
C2660.8138 (2)0.1269 (2)0.20160 (17)0.0175 (7)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
La10.01984 (11)0.01524 (11)0.01523 (11)0.00090 (8)0.00573 (9)0.00149 (8)
O110.0287 (13)0.0140 (12)0.0118 (12)−0.0005 (9)0.0047 (10)0.0019 (10)
C110.0182 (17)0.0146 (18)0.0135 (18)−0.0008 (13)0.0053 (14)−0.0005 (14)
C120.0186 (17)0.0147 (17)0.021 (2)−0.0002 (13)0.0051 (15)0.0013 (15)
C130.0160 (17)0.025 (2)0.030 (2)0.0045 (14)0.0088 (16)0.0090 (17)
C140.0215 (17)0.0109 (17)0.029 (2)0.0007 (13)0.0093 (16)0.0069 (15)
C150.0221 (18)0.0173 (18)0.026 (2)0.0030 (14)0.0123 (16)0.0027 (15)
C160.0193 (17)0.0178 (18)0.0192 (19)0.0009 (13)0.0058 (15)0.0034 (15)
N120.0276 (16)0.0204 (17)0.0254 (18)−0.0024 (13)0.0097 (14)0.0065 (14)
O1210.0415 (15)0.0174 (13)0.0232 (14)0.0038 (11)0.0181 (12)0.0048 (11)
O1220.0666 (19)0.0282 (15)0.0176 (15)0.0025 (13)0.0105 (14)0.0083 (12)
N140.0156 (16)0.0208 (17)0.050 (2)−0.0010 (13)0.0167 (16)−0.0034 (17)
O1410.0266 (14)0.0346 (16)0.059 (2)0.0072 (11)0.0092 (14)0.0413 (15)
O1420.0330 (14)0.0181 (14)0.0419 (17)0.0038 (11)0.0164 (13)0.0072 (12)
N160.0319 (17)0.0166 (16)0.0159 (16)−0.0054 (13)0.0049 (14)−0.0033 (13)
O1610.0430 (16)0.0284 (15)0.0223 (15)0.0105 (12)0.0052 (13)0.0056 (12)
O1620.0443 (16)0.0328 (15)0.0259 (15)0.0027 (12)0.0186 (13)−0.0015 (12)
O210.0258 (13)0.0267 (14)0.0153 (13)−0.0021 (10)0.0111 (11)−0.0025 (11)
C210.033 (2)0.0173 (18)0.026 (2)−0.0058 (15)0.0192 (18)0.0026 (16)
C220.031 (2)0.0229 (19)0.0126 (19)−0.0035 (15)0.0101 (16)0.0009 (15)
C230.045 (2)0.0204 (19)0.020 (2)−0.0112 (17)0.0147 (18)−0.0022 (16)
C240.046 (2)0.024 (2)0.025 (2)−0.0113 (17)0.027 (2)−0.0074 (16)
C250.040 (2)0.018 (2)0.044 (3)−0.0038 (16)0.029 (2)−0.0016 (18)
C260.0218 (18)0.0221 (19)0.030 (2)−0.0048 (15)0.0130 (17)0.0002 (16)
N220.0291 (18)0.0249 (17)0.0211 (19)0.0020 (13)0.0074 (15)0.0036 (14)
O2210.0267 (13)0.0288 (14)0.0185 (14)0.0031 (10)0.0056 (11)0.0049 (11)
O2220.0450 (17)0.0543 (19)0.0138 (15)0.0095 (14)−0.0029 (13)0.0099 (13)
N240.075 (3)0.0246 (19)0.038 (2)−0.0117 (19)0.037 (2)−0.0106 (17)
O2410.079 (2)0.063 (2)0.035 (2)−0.0212 (18)0.0286 (19)−0.0181 (17)
O2420.083 (2)0.049 (2)0.063 (2)0.0098 (17)0.053 (2)−0.0055 (17)
N260.0261 (18)0.039 (2)0.037 (2)−0.0019 (16)0.0168 (16)0.0081 (18)
O2610.0342 (15)0.0360 (17)0.0351 (17)−0.0069 (12)0.0152 (13)−0.0028 (14)
O2620.0366 (16)0.0430 (18)0.059 (2)0.0121 (14)0.0115 (15)0.0115 (16)
O310.0229 (13)0.0181 (13)0.0240 (14)0.0019 (10)0.0019 (11)0.0053 (11)
C310.027 (2)0.0204 (19)0.0133 (18)0.0027 (15)0.0064 (16)0.0040 (15)
C320.0235 (18)0.0128 (17)0.0120 (18)0.0038 (13)0.0051 (15)−0.0001 (14)
C330.0250 (19)0.0184 (18)0.0185 (19)−0.0001 (14)0.0062 (16)0.0039 (15)
C340.0224 (19)0.025 (2)0.024 (2)0.0021 (15)0.0079 (16)0.0043 (16)
C350.027 (2)0.025 (2)0.029 (2)0.0093 (15)0.0107 (17)0.0106 (17)
C360.037 (2)0.0097 (17)0.028 (2)0.0013 (15)0.0110 (18)0.0065 (15)
N320.0300 (17)0.0149 (16)0.0235 (17)0.0049 (13)0.0133 (15)0.0039 (13)
O3210.0219 (13)0.0217 (13)0.0265 (15)0.0044 (10)0.0044 (12)0.0057 (11)
O3220.0294 (13)0.0155 (13)0.0348 (16)−0.0002 (10)0.0107 (12)0.0009 (11)
N340.0213 (16)0.0269 (18)0.0275 (18)0.0019 (14)0.0058 (14)0.0114 (15)
O3410.0224 (13)0.0229 (14)0.0389 (16)−0.0030 (10)0.0045 (12)0.0094 (12)
O3420.0241 (14)0.0340 (16)0.0488 (18)0.0085 (12)0.0119 (13)0.0168 (14)
N360.0272 (18)0.0194 (17)0.048 (2)0.0000 (14)0.0021 (17)0.0027 (16)
O3610.022 (2)0.0260 (18)0.067 (6)0.003 (2)0.022 (3)−0.006 (5)
O3620.042 (4)0.019 (3)0.082 (6)0.005 (2)0.018 (4)0.015 (3)
O3630.022 (2)0.0260 (18)0.067 (6)0.003 (2)0.022 (3)−0.006 (5)
O3640.019 (4)0.012 (3)0.059 (8)0.004 (3)0.001 (4)0.009 (4)
O0110.0241 (13)0.0253 (13)0.0208 (14)−0.0024 (10)0.0121 (11)−0.0032 (11)
C0110.0196 (18)0.026 (2)0.026 (2)−0.0030 (15)0.0057 (16)−0.0008 (17)
C0120.061 (3)0.044 (3)0.047 (3)−0.018 (2)0.012 (2)0.000 (2)
O0210.0198 (12)0.0189 (12)0.0233 (14)0.0015 (9)0.0072 (11)0.0058 (10)
C0210.029 (2)0.0134 (18)0.028 (2)−0.0052 (14)0.0120 (17)0.0018 (15)
C0220.034 (2)0.029 (2)0.041 (3)−0.0041 (17)0.0141 (19)0.0195 (19)
O0310.0402 (15)0.0219 (13)0.0164 (13)0.0101 (11)0.0107 (12)0.0039 (11)
C0310.021 (3)0.032 (3)0.016 (3)0.007 (2)0.006 (2)0.000 (3)
C0320.027 (3)0.032 (4)0.018 (4)0.001 (3)−0.004 (3)0.005 (3)
O0330.0402 (15)0.0219 (13)0.0164 (13)0.0101 (11)0.0107 (12)0.0039 (11)
C0330.022 (6)0.030 (6)0.020 (6)0.020 (5)0.011 (5)0.006 (5)
C0340.020 (6)0.069 (9)0.015 (6)−0.006 (6)−0.005 (5)0.006 (6)
N1000.0185 (14)0.0234 (16)0.0115 (15)−0.0043 (11)0.0037 (12)0.0028 (12)
N1110.0232 (15)0.0219 (16)0.0180 (16)0.0032 (12)0.0089 (13)0.0056 (13)
C1120.0284 (19)0.0150 (18)0.034 (2)0.0044 (14)0.0125 (18)0.0099 (16)
C1130.0239 (19)0.034 (2)0.024 (2)0.0075 (15)0.0136 (16)0.0175 (17)
C1140.030 (2)0.030 (2)0.018 (2)0.0013 (16)0.0102 (16)0.0059 (16)
C1150.030 (2)0.0195 (19)0.023 (2)0.0024 (15)0.0090 (17)0.0034 (16)
C1160.0206 (17)0.0169 (18)0.0161 (18)0.0019 (13)0.0069 (15)0.0044 (14)
N1210.0236 (15)0.0234 (16)0.0195 (17)0.0019 (12)0.0081 (13)0.0058 (13)
C1220.030 (2)0.029 (2)0.017 (2)0.0036 (16)0.0106 (17)0.0074 (16)
C1230.029 (2)0.034 (2)0.019 (2)−0.0006 (16)0.0022 (17)0.0055 (17)
C1240.0208 (18)0.025 (2)0.032 (2)0.0013 (15)0.0029 (17)0.0080 (17)
C1250.0225 (18)0.0203 (19)0.024 (2)−0.0001 (14)0.0074 (16)0.0058 (16)
C1260.0266 (18)0.0143 (17)0.0156 (19)0.0048 (14)0.0088 (15)0.0046 (14)
N1310.0260 (16)0.0170 (15)0.0170 (16)−0.0005 (12)0.0080 (13)−0.0002 (12)
C1320.038 (2)0.0204 (19)0.018 (2)0.0005 (16)0.0139 (17)−0.0024 (15)
C1330.035 (2)0.0207 (19)0.0158 (19)−0.0013 (15)0.0100 (17)0.0013 (15)
C1340.041 (2)0.0196 (19)0.024 (2)0.0007 (16)0.0181 (18)0.0082 (16)
C1350.0276 (19)0.0223 (19)0.024 (2)0.0068 (15)0.0142 (16)0.0091 (16)
C1360.0244 (18)0.0198 (18)0.0119 (18)0.0028 (14)0.0101 (15)0.0036 (14)
La20.01786 (10)0.01719 (11)0.01533 (11)0.00167 (8)0.00620 (9)0.00436 (8)
O410.0261 (13)0.0195 (13)0.0140 (13)0.0030 (10)0.0061 (10)0.0069 (10)
C410.0237 (19)0.027 (2)0.0170 (19)0.0020 (15)0.0061 (16)0.0117 (16)
C420.0155 (16)0.0200 (18)0.0132 (18)0.0021 (13)0.0010 (14)0.0057 (14)
C430.0212 (18)0.0185 (18)0.021 (2)0.0008 (14)0.0084 (15)0.0004 (15)
C440.0115 (16)0.0227 (19)0.026 (2)0.0031 (13)0.0033 (15)0.0081 (16)
C450.0245 (18)0.0219 (19)0.024 (2)0.0028 (14)0.0113 (16)0.0119 (16)
C460.0181 (17)0.0219 (19)0.0117 (18)0.0032 (14)0.0048 (14)0.0037 (14)
N420.0223 (15)0.0203 (16)0.0158 (16)0.0039 (12)0.0028 (13)0.0050 (13)
O4210.0303 (13)0.0171 (13)0.0244 (14)0.0047 (10)0.0142 (11)0.0059 (11)
O4220.0536 (17)0.0242 (14)0.0150 (14)0.0003 (12)0.0048 (13)0.0034 (12)
N440.0181 (15)0.0219 (17)0.0276 (19)0.0099 (12)0.0111 (14)0.0195 (15)
O4410.0281 (14)0.0190 (14)0.052 (2)0.0045 (11)0.0117 (14)0.0090 (14)
O4420.0356 (15)0.0219 (14)0.0414 (17)0.0079 (11)0.0186 (14)0.0142 (13)
N460.0283 (17)0.0257 (17)0.0257 (18)0.0071 (14)0.0062 (15)0.0155 (15)
O4610.0443 (16)0.0310 (15)0.0212 (15)−0.0067 (12)0.0075 (13)0.0053 (12)
O4620.0447 (16)0.0469 (17)0.0263 (16)0.0057 (13)0.0215 (14)0.0098 (13)
O510.0227 (13)0.0273 (14)0.0172 (13)0.0091 (10)0.0092 (11)0.0074 (11)
C510.0253 (18)0.0133 (17)0.023 (2)0.0094 (14)0.0154 (16)0.0055 (15)
C520.0233 (19)0.025 (2)0.019 (2)0.0030 (15)0.0097 (16)0.0064 (16)
C530.036 (2)0.025 (2)0.0134 (19)0.0114 (16)0.0105 (16)0.0017 (15)
C540.042 (2)0.028 (2)0.020 (2)0.0139 (17)0.0205 (18)0.0130 (16)
C550.034 (2)0.029 (2)0.032 (2)0.0123 (16)0.0259 (19)0.0155 (17)
C560.0202 (18)0.0233 (19)0.030 (2)0.0120 (14)0.0131 (17)0.0092 (16)
N520.0325 (18)0.0217 (17)0.0200 (18)0.0098 (13)0.0082 (15)0.0054 (14)
O5210.0253 (13)0.0298 (14)0.0162 (14)0.0016 (10)0.0101 (11)0.0030 (11)
O5220.0377 (15)0.0375 (16)0.0178 (15)−0.0060 (12)0.0000 (12)−0.0020 (12)
N540.059 (2)0.038 (2)0.033 (2)0.0226 (18)0.033 (2)0.0180 (17)
O5410.072 (2)0.072 (2)0.0190 (17)0.0246 (17)0.0168 (16)0.0239 (16)
O5420.067 (2)0.060 (2)0.048 (2)0.0144 (16)0.0424 (17)0.0273 (16)
N560.0198 (16)0.042 (2)0.0283 (19)0.0070 (14)0.0143 (15)0.0080 (16)
O5610.0278 (14)0.0454 (17)0.0285 (16)0.0096 (12)0.0090 (12)0.0137 (14)
O5620.0331 (15)0.0415 (18)0.056 (2)−0.0073 (13)0.0128 (14)0.0125 (15)
O610.0164 (12)0.0200 (13)0.0191 (13)−0.0003 (9)0.0015 (10)0.0020 (10)
C610.029 (2)0.0175 (18)0.0067 (17)0.0013 (14)0.0067 (15)0.0016 (14)
C620.0248 (19)0.0228 (19)0.0176 (19)−0.0008 (15)0.0112 (16)0.0053 (15)
C630.0270 (19)0.0178 (18)0.0156 (18)0.0046 (14)0.0095 (15)0.0045 (14)
C640.0130 (16)0.028 (2)0.0081 (17)0.0004 (14)0.0019 (13)0.0005 (14)
C650.0160 (17)0.0231 (19)0.0177 (19)−0.0020 (14)0.0074 (15)0.0020 (15)
C660.0202 (18)0.0207 (19)0.0193 (19)−0.0003 (14)0.0034 (15)0.0047 (15)
N620.0206 (16)0.0155 (15)0.0204 (16)−0.0005 (12)0.0061 (13)0.0037 (13)
O6210.0191 (13)0.0212 (13)0.0238 (14)−0.0021 (10)0.0026 (11)0.0049 (11)
O6220.0285 (14)0.0266 (14)0.0383 (16)−0.0003 (11)0.0035 (12)0.0221 (13)
N640.0223 (16)0.0223 (17)0.0237 (18)0.0031 (13)0.0092 (14)0.0048 (14)
O6410.0236 (13)0.0247 (14)0.0284 (15)0.0079 (10)0.0060 (11)0.0070 (12)
O6420.0251 (13)0.0275 (14)0.0419 (17)−0.0035 (11)0.0120 (12)0.0091 (12)
N660.0282 (17)0.0233 (17)0.036 (2)0.0043 (14)0.0143 (16)0.0140 (15)
O6610.0201 (13)0.0354 (15)0.0474 (18)0.0043 (11)0.0024 (13)0.0239 (14)
O6620.0396 (16)0.0194 (14)0.0534 (19)−0.0042 (12)0.0088 (14)0.0108 (13)
O0410.0208 (12)0.0295 (13)0.0157 (13)0.0053 (10)0.0078 (10)0.0096 (11)
C0410.0136 (17)0.034 (2)0.025 (2)−0.0005 (15)0.0003 (15)0.0138 (17)
C0420.052 (3)0.046 (3)0.047 (3)0.031 (2)0.012 (2)0.018 (2)
O0510.0216 (12)0.0121 (11)0.0206 (13)0.0007 (9)0.0084 (10)−0.0027 (10)
C0510.0234 (18)0.0171 (19)0.024 (2)0.0079 (14)0.0082 (16)0.0048 (15)
C0520.035 (2)0.0184 (19)0.027 (2)0.0038 (15)0.0124 (18)−0.0104 (16)
O0610.0280 (13)0.0166 (12)0.0167 (13)−0.0024 (9)0.0101 (11)0.0010 (10)
C0610.031 (2)0.025 (2)0.0096 (18)−0.0022 (15)0.0097 (16)−0.0005 (15)
C0620.027 (2)0.030 (2)0.022 (2)0.0034 (16)0.0104 (17)0.0019 (17)
N2000.0221 (15)0.0206 (15)0.0164 (16)0.0046 (12)0.0094 (13)0.0045 (12)
N2410.0189 (15)0.0159 (15)0.0224 (17)0.0032 (11)0.0097 (13)0.0041 (13)
C2420.0175 (17)0.0177 (18)0.029 (2)0.0029 (14)0.0037 (16)0.0027 (16)
C2430.0216 (18)0.023 (2)0.021 (2)−0.0001 (14)0.0065 (16)−0.0075 (16)
C2440.0273 (19)0.029 (2)0.0150 (19)−0.0016 (15)0.0105 (16)0.0055 (16)
C2450.0270 (18)0.0154 (17)0.0163 (19)−0.0013 (14)0.0087 (15)0.0008 (14)
C2460.0198 (17)0.0177 (18)0.0171 (19)0.0016 (13)0.0050 (15)−0.0002 (15)
N2510.0269 (16)0.0219 (16)0.0163 (16)0.0029 (12)0.0106 (13)0.0012 (13)
C2520.034 (2)0.0238 (19)0.0110 (18)0.0002 (15)0.0107 (16)−0.0033 (15)
C2530.037 (2)0.027 (2)0.0125 (19)0.0038 (16)−0.0023 (17)0.0021 (16)
C2540.0242 (19)0.026 (2)0.025 (2)0.0025 (15)0.0024 (17)−0.0005 (17)
C2550.0159 (17)0.030 (2)0.021 (2)0.0053 (14)0.0027 (15)0.0079 (16)
C2560.0256 (18)0.0105 (17)0.0165 (19)0.0020 (13)0.0052 (15)−0.0008 (14)
N2610.0222 (15)0.0160 (15)0.0147 (15)0.0007 (11)0.0035 (13)0.0024 (12)
C2620.0235 (19)0.027 (2)0.020 (2)−0.0004 (15)0.0011 (16)0.0077 (16)
C2630.029 (2)0.031 (2)0.028 (2)0.0119 (16)0.0104 (18)0.0156 (18)
C2640.0279 (19)0.0153 (18)0.028 (2)0.0024 (14)0.0100 (17)0.0021 (16)
C2650.0254 (18)0.0165 (18)0.0119 (18)−0.0001 (14)0.0026 (15)−0.0018 (14)
C2660.0239 (18)0.0203 (18)0.0129 (18)0.0065 (14)0.0083 (15)0.0105 (14)
Geometric parameters (Å, º) top
La1—O112.418 (2)C134—C1351.379 (4)
La1—O312.422 (2)C134—H1340.9500
La1—O212.423 (2)C135—C1361.382 (4)
La1—O0212.501 (2)C135—H1350.9500
La1—O0112.507 (2)La2—O412.404 (2)
La1—O0312.508 (2)La2—O612.415 (2)
La1—O1212.623 (2)La2—O512.423 (2)
La1—O3212.648 (2)La2—O0412.506 (2)
La1—O2212.758 (2)La2—O0512.515 (2)
O11—C111.273 (3)La2—O0612.516 (2)
C11—C121.431 (4)La2—O4212.624 (2)
C11—C161.443 (4)La2—O6212.702 (2)
C12—C131.373 (4)La2—O5212.759 (2)
C12—N121.454 (4)O41—C411.272 (4)
C13—C141.369 (4)C41—C421.432 (4)
C13—H130.9500C41—C461.435 (4)
C14—C151.388 (5)C42—C431.381 (4)
C14—N141.471 (4)C42—N421.461 (4)
C15—C161.357 (4)C43—C441.378 (4)
C15—H150.9500C43—H430.9500
C16—N161.476 (4)C44—C451.397 (5)
N12—O1221.228 (4)C44—N441.504 (4)
N12—O1211.240 (3)C45—C461.361 (4)
N14—O1411.183 (4)C45—H450.9500
N14—O1421.245 (4)C46—N461.474 (4)
N16—O1611.226 (3)N42—O4221.220 (3)
N16—O1621.234 (3)N42—O4211.245 (3)
O21—C211.265 (4)N44—O4411.175 (3)
C21—C221.431 (5)N44—O4421.223 (3)
C21—C261.435 (5)N46—O4611.223 (3)
C22—C231.387 (4)N46—O4621.226 (3)
C22—N221.465 (4)O51—C511.270 (4)
C23—C241.378 (5)C51—C521.430 (5)
C23—H230.9500C51—C561.435 (4)
C24—C251.384 (5)C52—C531.387 (4)
C24—N241.467 (4)C52—N521.447 (4)
C25—C261.369 (5)C53—C541.375 (5)
C25—H250.9500C53—H530.9500
C26—N261.474 (5)C54—C551.381 (5)
N22—O2221.220 (4)C54—N541.461 (4)
N22—O2211.236 (3)C55—C561.377 (4)
N24—O2411.225 (4)C55—H550.9500
N24—O2421.236 (4)C56—N561.461 (4)
N26—O2621.226 (4)N52—O5221.234 (3)
N26—O2611.229 (4)N52—O5211.238 (3)
O31—C311.272 (4)N54—O5411.218 (4)
C31—C361.439 (5)N54—O5421.240 (4)
C31—C321.442 (4)N56—O5611.230 (4)
C32—C331.377 (4)N56—O5621.231 (4)
C32—N321.463 (4)O61—C611.263 (4)
C33—C341.360 (4)C61—C661.444 (4)
C33—H330.9500C61—C621.450 (5)
C34—C351.388 (4)C62—C631.386 (4)
C34—N341.464 (4)C62—N621.456 (4)
C35—C361.369 (5)C63—C641.395 (4)
C35—H350.9500C63—H630.9500
C36—N361.468 (4)C64—C651.384 (4)
N32—O3221.232 (3)C64—N641.456 (4)
N32—O3211.242 (3)C65—C661.361 (4)
N34—O3411.225 (3)C65—H650.9500
N34—O3421.237 (3)C66—N661.473 (4)
N36—O3631.214 (12)N62—O6221.237 (3)
N36—O3611.227 (9)N62—O6211.239 (3)
N36—O3621.244 (7)N64—O6411.223 (3)
N36—O3641.282 (9)N64—O6421.237 (3)
O011—C0111.453 (4)N66—O6621.229 (3)
O011—H0110.8400N66—O6611.231 (3)
C011—C0121.484 (5)O041—C0411.445 (4)
C011—H01A0.9900O041—H0410.8400
C011—H01B0.9900C041—C0421.512 (5)
C012—H01C0.9800C041—H04A0.9900
C012—H01D0.9800C041—H04B0.9900
C012—H01E0.9800C042—H04C0.9800
O021—C0211.446 (3)C042—H04D0.9800
O021—H0210.8400C042—H04E0.9800
C021—C0221.501 (5)O051—C0511.441 (4)
C021—H02A0.9900O051—H0510.8402
C021—H02B0.9900C051—C0521.499 (4)
C022—H02C0.9800C051—H05A0.9900
C022—H02D0.9800C051—H05B0.9900
C022—H02E0.9800C052—H05C0.9800
O031—C0311.476 (6)C052—H05D0.9800
O031—H0310.8396C052—H05E0.9800
O031—H0330.8393O061—C0611.439 (4)
C031—C0321.488 (7)O061—H0610.8401
C031—H03A0.9900C061—C0621.514 (4)
C031—H03B0.9900C061—H06A0.9900
C032—H03C0.9800C061—H06B0.9900
C032—H03D0.9800C062—H06C0.9800
C032—H03E0.9800C062—H06D0.9800
C033—C0341.489 (12)C062—H06E0.9800
C033—H03F0.9900N200—C2461.421 (4)
C033—H03G0.9900N200—C2561.424 (4)
C034—H03H0.9800N200—C2661.426 (4)
C034—H03I0.9800N241—C2461.336 (4)
C034—H03J0.9800N241—C2421.352 (4)
N100—C1261.415 (4)C242—C2431.379 (5)
N100—C1361.426 (4)C242—H2420.9500
N100—C1161.428 (4)C243—C2441.377 (5)
N111—C1161.334 (4)C243—H2430.9500
N111—C1121.349 (4)C244—C2451.382 (4)
C112—C1131.378 (5)C244—H2440.9500
C112—H1120.9500C245—C2461.379 (4)
C113—C1141.376 (5)C245—H2450.9500
C113—H1130.9500N251—C2561.325 (4)
C114—C1151.383 (4)N251—C2521.343 (4)
C114—H1140.9500C252—C2531.366 (5)
C115—C1161.382 (4)C252—H2520.9500
C115—H1150.9500C253—C2541.390 (5)
N121—C1261.340 (4)C253—H2530.9500
N121—C1221.340 (4)C254—C2551.379 (5)
C122—C1231.368 (5)C254—H2540.9500
C122—H1220.9500C255—C2561.400 (4)
C123—C1241.393 (5)C255—H2550.9500
C123—H1230.9500N261—C2661.340 (4)
C124—C1251.379 (5)N261—C2621.341 (4)
C124—H1240.9500C262—C2631.377 (5)
C125—C1261.392 (4)C262—H2620.9500
C125—H1250.9500C263—C2641.386 (5)
N131—C1361.336 (4)C263—H2630.9500
N131—C1321.356 (4)C264—C2651.373 (4)
C132—C1331.369 (5)C264—H2640.9500
C132—H1320.9500C265—C2661.384 (4)
C133—C1341.379 (5)C265—H2650.9500
C133—H1330.9500
O11···O0113.217 (3)O41···O0413.115 (4)
O21···O0213.341 (3)O51···O0513.397 (4)
O31···O0313.400 (4)O61···O0613.483 (4)
O11—La1—O3183.56 (7)C133—C134—H134120.0
O11—La1—O2177.24 (7)C134—C135—C136117.7 (3)
O31—La1—O2178.13 (8)C134—C135—H135121.2
O11—La1—O021135.75 (7)C136—C135—H135121.2
O31—La1—O021132.33 (7)N131—C136—C135123.7 (3)
O21—La1—O02185.43 (7)N131—C136—N100115.6 (3)
O11—La1—O01181.53 (7)C135—C136—N100120.6 (3)
O31—La1—O011140.19 (7)O41—La2—O6184.07 (7)
O21—La1—O011132.99 (7)O41—La2—O5178.16 (7)
O021—La1—O01181.35 (7)O61—La2—O5179.12 (7)
O11—La1—O031132.41 (7)O41—La2—O04178.73 (7)
O31—La1—O03187.21 (8)O61—La2—O041139.58 (7)
O21—La1—O031145.42 (7)O51—La2—O041131.15 (7)
O021—La1—O03181.64 (7)O41—La2—O051136.73 (7)
O011—La1—O03176.40 (7)O61—La2—O051132.83 (7)
O11—La1—O12164.93 (7)O51—La2—O05186.93 (7)
O31—La1—O12167.28 (7)O041—La2—O05181.41 (7)
O21—La1—O121130.43 (7)O41—La2—O061132.65 (7)
O021—La1—O121144.13 (7)O61—La2—O06189.85 (7)
O011—La1—O12172.96 (7)O51—La2—O061146.34 (7)
O031—La1—O12168.43 (7)O041—La2—O06176.13 (7)
O11—La1—O321139.95 (7)O051—La2—O06177.46 (7)
O31—La1—O32163.77 (7)O41—La2—O42165.29 (7)
O21—La1—O32174.00 (7)O61—La2—O42166.78 (7)
O021—La1—O32168.73 (7)O51—La2—O421131.44 (7)
O011—La1—O321138.46 (7)O041—La2—O42172.81 (7)
O031—La1—O32171.43 (7)O051—La2—O421141.63 (7)
O121—La1—O321116.62 (7)O061—La2—O42169.19 (7)
O11—La1—O22170.14 (7)O41—La2—O621139.50 (7)
O31—La1—O221136.22 (7)O61—La2—O62162.92 (7)
O21—La1—O22162.61 (7)O51—La2—O62173.33 (7)
O021—La1—O22165.73 (7)O041—La2—O621141.71 (7)
O011—La1—O22170.84 (7)O051—La2—O62169.92 (7)
O031—La1—O221136.31 (7)O061—La2—O62173.33 (7)
O121—La1—O221125.17 (7)O421—La2—O621115.75 (7)
O321—La1—O221117.88 (7)O41—La2—O52171.61 (7)
C11—O11—La1141.63 (19)O61—La2—O521137.79 (7)
O11—C11—C12126.4 (3)O51—La2—O52162.72 (7)
O11—C11—C16121.0 (3)O041—La2—O52169.31 (7)
C12—C11—C16112.6 (3)O051—La2—O52165.47 (7)
C13—C12—C11123.2 (3)O061—La2—O521131.97 (6)
C13—C12—N12116.6 (3)O421—La2—O521126.73 (7)
C11—C12—N12120.3 (3)O621—La2—O521117.28 (7)
C14—C13—C12119.7 (3)C41—O41—La2142.7 (2)
C14—C13—H13120.1O41—C41—C42125.7 (3)
C12—C13—H13120.1O41—C41—C46120.9 (3)
C13—C14—C15121.3 (3)C42—C41—C46113.4 (3)
C13—C14—N14118.3 (3)C43—C42—C41123.1 (3)
C15—C14—N14120.3 (3)C43—C42—N42115.6 (3)
C16—C15—C14118.4 (3)C41—C42—N42121.3 (3)
C16—C15—H15120.8C44—C43—C42119.0 (3)
C14—C15—H15120.8C44—C43—H43120.5
C15—C16—C11124.7 (3)C42—C43—H43120.5
C15—C16—N16118.8 (3)C43—C44—C45121.7 (3)
C11—C16—N16116.5 (3)C43—C44—N44118.2 (3)
O122—N12—O121121.9 (3)C45—C44—N44120.1 (3)
O122—N12—C12118.9 (3)C46—C45—C44118.0 (3)
O121—N12—C12119.1 (3)C46—C45—H45121.0
N12—O121—La1133.32 (19)C44—C45—H45121.0
O141—N14—O142123.4 (3)C45—C46—C41124.6 (3)
O141—N14—C14121.0 (3)C45—C46—N46118.9 (3)
O142—N14—C14115.6 (3)C41—C46—N46116.4 (3)
O161—N16—O162124.4 (3)O422—N42—O421121.8 (3)
O161—N16—C16118.7 (3)O422—N42—C42119.2 (3)
O162—N16—C16116.9 (3)O421—N42—C42118.9 (3)
C21—O21—La1132.25 (19)N42—O421—La2135.20 (18)
O21—C21—C22125.0 (3)O441—N44—O442128.1 (3)
O21—C21—C26122.7 (3)O441—N44—C44117.6 (3)
C22—C21—C26112.3 (3)O442—N44—C44114.2 (3)
C23—C22—C21124.5 (3)O461—N46—O462125.2 (3)
C23—C22—N22115.8 (3)O461—N46—C46117.6 (3)
C21—C22—N22119.7 (3)O462—N46—C46117.2 (3)
C24—C23—C22118.1 (3)C51—O51—La2133.24 (19)
C24—C23—H23121.0O51—C51—C52125.6 (3)
C22—C23—H23121.0O51—C51—C56121.5 (3)
C23—C24—C25121.8 (3)C52—C51—C56112.9 (3)
C23—C24—N24118.5 (4)C53—C52—C51123.9 (3)
C25—C24—N24119.7 (4)C53—C52—N52116.7 (3)
C26—C25—C24118.6 (3)C51—C52—N52119.4 (3)
C26—C25—H25120.7C54—C53—C52118.8 (3)
C24—C25—H25120.7C54—C53—H53120.6
C25—C26—C21124.6 (3)C52—C53—H53120.6
C25—C26—N26116.6 (3)C53—C54—C55121.4 (3)
C21—C26—N26118.8 (3)C53—C54—N54118.8 (3)
O222—N22—O221122.7 (3)C55—C54—N54119.7 (3)
O222—N22—C22118.5 (3)C56—C55—C54119.0 (3)
O221—N22—C22118.8 (3)C56—C55—H55120.5
N22—O221—La1137.2 (2)C54—C55—H55120.5
O241—N24—O242124.9 (4)C55—C56—C51123.8 (3)
O241—N24—C24117.8 (4)C55—C56—N56117.8 (3)
O242—N24—C24117.3 (4)C51—C56—N56118.2 (3)
O262—N26—O261125.1 (3)O522—N52—O521122.1 (3)
O262—N26—C26117.2 (3)O522—N52—C52118.0 (3)
O261—N26—C26117.7 (3)O521—N52—C52119.9 (3)
C31—O31—La1142.0 (2)N52—O521—La2136.9 (2)
O31—C31—C36122.9 (3)O541—N54—O542124.1 (3)
O31—C31—C32124.0 (3)O541—N54—C54118.5 (3)
C36—C31—C32113.0 (3)O542—N54—C54117.3 (4)
C33—C32—C31123.0 (3)O561—N56—O562123.6 (3)
C33—C32—N32115.7 (3)O561—N56—C56118.7 (3)
C31—C32—N32121.2 (3)O562—N56—C56117.6 (3)
C34—C33—C32119.6 (3)C61—O61—La2141.8 (2)
C34—C33—H33120.2O61—C61—C66123.7 (3)
C32—C33—H33120.2O61—C61—C62124.1 (3)
C33—C34—C35121.9 (3)C66—C61—C62112.0 (3)
C33—C34—N34119.0 (3)C63—C62—C61124.2 (3)
C35—C34—N34119.1 (3)C63—C62—N62115.4 (3)
C36—C35—C34118.6 (3)C61—C62—N62120.4 (3)
C36—C35—H35120.7C62—C63—C64118.2 (3)
C34—C35—H35120.7C62—C63—H63120.9
C35—C36—C31123.9 (3)C64—C63—H63120.9
C35—C36—N36115.7 (3)C65—C64—C63121.6 (3)
C31—C36—N36120.5 (3)C65—C64—N64119.4 (3)
O322—N32—O321121.2 (3)C63—C64—N64119.0 (3)
O322—N32—C32118.5 (3)C66—C65—C64119.1 (3)
O321—N32—C32120.2 (3)C66—C65—H65120.4
N32—O321—La1142.00 (19)C64—C65—H65120.4
O341—N34—O342124.2 (3)C65—C66—C61124.9 (3)
O341—N34—C34118.8 (3)C65—C66—N66116.8 (3)
O342—N34—C34117.0 (3)C61—C66—N66118.3 (3)
O361—N36—O362121.4 (12)O622—N62—O621121.7 (3)
O363—N36—O364125.0 (16)O622—N62—C62118.1 (3)
O363—N36—C36119.4 (17)O621—N62—C62120.3 (3)
O361—N36—C36119.5 (12)N62—O621—La2140.69 (18)
O362—N36—C36118.6 (4)O641—N64—O642123.7 (3)
O364—N36—C36114.4 (5)O641—N64—C64119.0 (3)
C011—O011—La1129.85 (18)O642—N64—C64117.3 (3)
C011—O011—H011109.5O662—N66—O661123.3 (3)
La1—O011—H011120.5O662—N66—C66117.0 (3)
O011—C011—C012112.2 (3)O661—N66—C66119.6 (3)
O011—C011—H01A109.2C041—O041—La2131.51 (17)
C012—C011—H01A109.2C041—O041—H041109.5
O011—C011—H01B109.2La2—O041—H041118.6
C012—C011—H01B109.2O041—C041—C042112.2 (3)
H01A—C011—H01B107.9O041—C041—H04A109.2
C011—C012—H01C109.5C042—C041—H04A109.2
C011—C012—H01D109.5O041—C041—H04B109.2
H01C—C012—H01D109.5C042—C041—H04B109.2
C011—C012—H01E109.5H04A—C041—H04B107.9
H01C—C012—H01E109.5C041—C042—H04C109.5
H01D—C012—H01E109.5C041—C042—H04D109.5
C021—O021—La1127.51 (18)H04C—C042—H04D109.5
C021—O021—H021109.5C041—C042—H04E109.5
La1—O021—H021119.5H04C—C042—H04E109.5
O021—C021—C022112.0 (3)H04D—C042—H04E109.5
O021—C021—H02A109.2C051—O051—La2126.94 (17)
C022—C021—H02A109.2C051—O051—H051109.5
O021—C021—H02B109.2La2—O051—H051118.4
C022—C021—H02B109.2O051—C051—C052111.7 (3)
H02A—C021—H02B107.9O051—C051—H05A109.3
C021—C022—H02C109.5C052—C051—H05A109.3
C021—C022—H02D109.5O051—C051—H05B109.3
H02C—C022—H02D109.5C052—C051—H05B109.3
C021—C022—H02E109.5H05A—C051—H05B107.9
H02C—C022—H02E109.5C051—C052—H05C109.5
H02D—C022—H02E109.5C051—C052—H05D109.5
C031—O031—La1138.2 (2)H05C—C052—H05D109.5
C031—O031—H031109.4C051—C052—H05E109.5
La1—O031—H031109.9H05C—C052—H05E109.5
C031—O031—H033103.8H05D—C052—H05E109.5
La1—O031—H033117.8C061—O061—La2135.52 (17)
O031—C031—C032106.2 (4)C061—O061—H061109.5
O031—C031—H03A110.5La2—O061—H061113.9
C032—C031—H03A110.5O061—C061—C062110.5 (3)
O031—C031—H03B110.5O061—C061—H06A109.6
C032—C031—H03B110.5C062—C061—H06A109.6
H03A—C031—H03B108.7O061—C061—H06B109.5
C031—C032—H03C109.5C062—C061—H06B109.5
C031—C032—H03D109.5H06A—C061—H06B108.1
H03C—C032—H03D109.5C061—C062—H06C109.5
C031—C032—H03E109.5C061—C062—H06D109.5
H03C—C032—H03E109.5H06C—C062—H06D109.5
H03D—C032—H03E109.5C061—C062—H06E109.5
C034—C033—H03F110.2H06C—C062—H06E109.5
C034—C033—H03G110.2H06D—C062—H06E109.5
H03F—C033—H03G108.5C246—N200—C256120.8 (3)
C033—C034—H03H109.5C246—N200—C266119.9 (3)
C033—C034—H03I109.5C256—N200—C266118.8 (3)
H03H—C034—H03I109.5C246—N241—C242117.3 (3)
C033—C034—H03J109.5N241—C242—C243123.0 (3)
H03H—C034—H03J109.5N241—C242—H242118.5
H03I—C034—H03J109.5C243—C242—H242118.5
C126—N100—C136119.9 (2)C244—C243—C242117.9 (3)
C126—N100—C116120.2 (2)C244—C243—H243121.0
C136—N100—C116119.8 (3)C242—C243—H243121.0
C116—N111—C112116.8 (3)C243—C244—C245120.5 (3)
N111—C112—C113123.4 (3)C243—C244—H244119.8
N111—C112—H112118.3C245—C244—H244119.8
C113—C112—H112118.3C246—C245—C244117.4 (3)
C114—C113—C112118.6 (3)C246—C245—H245121.3
C114—C113—H113120.7C244—C245—H245121.3
C112—C113—H113120.7N241—C246—C245123.9 (3)
C113—C114—C115119.2 (3)N241—C246—N200115.4 (3)
C113—C114—H114120.4C245—C246—N200120.7 (3)
C115—C114—H114120.4C256—N251—C252117.7 (3)
C114—C115—C116118.3 (3)N251—C252—C253123.4 (3)
C114—C115—H115120.9N251—C252—H252118.3
C116—C115—H115120.9C253—C252—H252118.3
N111—C116—C115123.7 (3)C252—C253—C254118.4 (3)
N111—C116—N100115.1 (3)C252—C253—H253120.8
C115—C116—N100121.2 (3)C254—C253—H253120.8
C126—N121—C122117.8 (3)C255—C254—C253119.5 (3)
N121—C122—C123123.6 (3)C255—C254—H254120.3
N121—C122—H122118.2C253—C254—H254120.3
C123—C122—H122118.2C254—C255—C256117.6 (3)
C122—C123—C124118.5 (3)C254—C255—H255121.2
C122—C123—H123120.8C256—C255—H255121.2
C124—C123—H123120.8N251—C256—C255123.3 (3)
C125—C124—C123118.9 (3)N251—C256—N200117.7 (3)
C125—C124—H124120.5C255—C256—N200119.0 (3)
C123—C124—H124120.5C266—N261—C262116.5 (3)
C124—C125—C126118.7 (3)N261—C262—C263124.3 (3)
C124—C125—H125120.6N261—C262—H262117.9
C126—C125—H125120.6C263—C262—H262117.9
N121—C126—C125122.4 (3)C262—C263—C264117.7 (3)
N121—C126—N100116.5 (3)C262—C263—H263121.1
C125—C126—N100121.0 (3)C264—C263—H263121.1
C136—N131—C132117.0 (3)C265—C264—C263119.4 (3)
N131—C132—C133123.2 (3)C265—C264—H264120.3
N131—C132—H132118.4C263—C264—H264120.3
C133—C132—H132118.4C264—C265—C266118.6 (3)
C132—C133—C134118.3 (3)C264—C265—H265120.7
C132—C133—H133120.8C266—C265—H265120.7
C134—C133—H133120.8N261—C266—C265123.3 (3)
C135—C134—C133120.1 (3)N261—C266—N200115.4 (3)
C135—C134—H134120.0C265—C266—N200121.3 (3)
N111—C116—N100—C12642.2 (4)N241—C246—N200—C25641.8 (4)
N121—C126—N100—C13638.1 (4)N251—C256—N200—C26636.9 (4)
N131—C136—N100—C11640.1 (4)N261—C266—N200—C24634.0 (5)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O011—H011···N1110.8391.9022.740 (4)175
O021—H021···N1210.8401.9162.747 (3)170
O031—H031···N1310.8401.8952.693 (3)158
O041—H041···N241i0.8391.8812.721 (4)179
O051—H051···N251i0.8411.9342.769 (3)172
O061—H061···N261i0.8401.8542.692 (4)175
Symmetry code: (i) x, y+1, z.

Experimental details

Crystal data
Chemical formula[La(C6H2N3O7)3(C2H6O)3]·C15H12N4
Mr1209.69
Crystal system, space groupTriclinic, P1
Temperature (K)100
a, b, c (Å)15.7554 (19), 16.4752 (14), 20.427 (4)
α, β, γ (°)101.714 (11), 111.610 (14), 90.676 (8)
V (Å3)4805.1 (13)
Z4
Radiation typeMo Kα
µ (mm−1)0.99
Crystal size (mm)0.50 × 0.18 × 0.03
Data collection
DiffractometerOxford Diffraction Xcalibur
diffractometer
Absorption correctionMulti-scan
(CrysAlis RED; Oxford Diffraction, 2006)
Tmin, Tmax0.773, 0.970
No. of measured, independent and
observed [I > 2σ(I)] reflections		58832, 28469, 14209
Rint0.049
(sin θ/λ)max (Å−1)0.728
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.043, 0.086, 0.84
No. of reflections28469
No. of parameters1419
No. of restraints104
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å−3)2.85, −0.75

Computer programs: CrysAlis CCD (Oxford Diffraction, 2006), CrysAlis RED (Oxford Diffraction, 2006), SIR92 (Altomare et al., 1994), SHELXL97 (Sheldrick, 2008), Xtal3.7 (Hall et al., 2001).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O011—H011···N1110.8391.9022.740 (4)175
O021—H021···N1210.8401.9162.747 (3)170
O031—H031···N1310.8401.8952.693 (3)158
O041—H041···N241i0.8391.8812.721 (4)179
O051—H051···N251i0.8411.9342.769 (3)172
O061—H061···N261i0.8401.8542.692 (4)175
Symmetry code: (i) x, y+1, z.
 

Acknowledgements

The author thanks Dr Brian Skelton, University of Western Australia Crystallography Centre, for assistance during the data collection and Professor Allan White, University of Western Australia School of Biomedical and Chemical Sciences, for supplying the starting materials.

References

First citationAltomare, A., Cascarano, G., Giacovazzo, C., Guagliardi, A., Burla, M. C., Polidori, G. & Camalli, M. (1994). J. Appl. Cryst. 27, 435.  CrossRef Web of Science IUCr Journals Google Scholar
 First citationChan, E. J. (2006). Doctoral Thesis, School of Biomedical and Chemical Sciences, UWA, Australia.  Google Scholar
 First citationHall, S. R., du Boulay, D. J. & Olthof-Hazekamp, R. (2001). The Xtal3.7 System. The University of Western Australia, Australia.  Google Scholar
 First citationHarrowfield, J. (1996). J. Chem. Soc. Dalton Trans. pp. 3165–3171.  CrossRef Web of Science Google Scholar
 First citationHarrowfield, J. M., Skelton, B. W. & White, A. H. (1994). Aust. J. Chem. 47, 359–364.  CrossRef CAS Google Scholar
 First citationKepert, D. L. (1986). Inorganic Stereochemistry. Berlin: Springer-Verlag.  Google Scholar
 First citationNagao, N., Egashira, K. & Mogi, D. (2004). Bull. Chem. Soc. Jpn, 77, 1171–1172.  Web of Science CSD CrossRef CAS Google Scholar
 First citationOxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Abingdon, Oxfordshire, England.  Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

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ISSN: 2056-9890
Volume 64| Part 8| August 2008| Pages m984-m985
doi:10.1107/S1600536808019296
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