research communications
Synthesis, κN)tetrakis(4-methoxypyridine-κN)cobalt(II)
and properties of bis(isoselenocyanato-aInstitut für Anorganische Chemie, Universität Kiel, Max-Eyth-Str. 2, 24118 Kiel, Germany
*Correspondence e-mail: cnaether@ac.uni-kiel.de
Reaction of CoCl2·6H2O with KNCSe and 4-methoxypyridine in water led to the formation of the title compound, [Co(NCSe)2(C6H7NO)4] or Co(NCSe)2(4-methoxypyridine)2, which was characterized by single-crystal X-ray diffraction. Its consists of one crystallographically independent Co cation, two selenocyanate anions and four 4-methoxypyridine coligands in general positions. In the the cobalt cations are sixfold coordinated by two terminal N-bonded selenocyanate anions and four 4-methoxypyridine coligands within a slightly distorted octahedral coordination. Between the complexes, weak C—H⋯Se interactions are found. IR spectroscopic investigations revealed that the CN stretching vibration of the anionic ligands is observed at 2068 cm−1, which is in agreement with the presence of only terminally coordinated selenocyanate anions. PXRD measurements prove that a pure compound was obtained. Differential thermoanalysis coupled to thermogravimetry (DTA-TG) at different heating rates shows that the TG curves are poorly resolved. PXRD measurements of the residue obtained by a TG measurement prove that an amorphous compound was obtained.
CCDC reference: 2242297
1. Chemical context
Coordination compounds based on transition-metal thiocyanates show versatile structural behavior (Buckingham, 1994; Barnett et al., 2002; Werner et al., 2015) and promising magnetic properties, because this ligand is able to mediate reasonable magnetic exchange (Barasiński et al., 2010; Palion-Gazda et al., 2015; Mousavi et al., 2020). In this context, compounds based on Co(NCS)2 are of special interest because they can show interesting magnetic behavior, such as, for example, slow relaxations of the magnetization, which is indicative of single-chain magnetism (Lescouëzec et al., 2005; Sun et al., 2010; Dhers et al., 2015). For the synthesis of such compounds, the CoII cations must be linked via the anionic ligands into mono-periodic or di-periodic networks. Compounds with di-periodicity are rare; the majority of compounds being mono-periodic, in which the CoII cations are octahedrally coordinated and linked into chains by pairs of anionic ligands (Guang et al., 2007; Shi et al., 2007; Shurdha et al., 2013; Prananto et al., 2017). If the chains are linear, ferromagnetic ordering (Werner et al., 2014) or single-chain magnet behavior (Mautner et al., 2018) is observed and if they are corrugated or exhibit an alternating Co coordination, the magnetic exchange is weak or completely suppressed (Dockum et al., 1983; Böhme et al., 2020, 2022). All this is well investigated for Co(NCS)2 compounds but not much is known for compounds based on Co(NCSe)2, because only two compounds with μ-1,3-bridging selenocyanate anions are reported in the literature (Boeckmann et al., 2011; Wöhlert et al., 2012; Neumann et al., 2019). First results indicate that they behave in a similar manner to their thiocyanate analogs and that the exchange of thio- by selenocyanate leads to an increase in the magnetic intrachain interactions (Neumann et al., 2019).
Unfortunately, the synthesis of compounds in which CoII cations are linked by selenocyanate anions into chains in solution is always difficult to achieve or even impossible, because CoII is not very chalcophilic and therefore, in most cases, compounds with terminally coordinated selenocyanate anions are obtained. To overcome this problem, we have developed an alternative approach for the synthesis of coordination networks based on thermal ligand removal of suitable precursor compounds that can be used for the synthesis of a wide range of materials including thio- and selenocyanates but also halide coordination compounds (Werner et al., 2014; Boeckmann et al., 2011; Näther & Jess, 2004). For thiocyanate compounds, the precursors usually consist of discrete complexes of the general formula Co(NCS)2(L)4 (L = mono-coordinating coligand), in which the CoII cations are octahedrally coordinated by two terminal N-bonded thiocyanate anions and four coligands. Upon heating, most of compounds of this type lose half of the ligands in the first mass loss and the octahedral metal coordination is retained by the sulfur atoms that were not involved in the metal coordination in the precursor, which enforces the formation of compounds with bridging anionic ligands.
In the course of our systematic work we became interested in the corresponding Co(NCSe)2 compounds with 4-methoxypyridine as coligand, because its thiocyanate analog Co(NCS)2(4-methoxypyridine)2 crystallizes in the desired chain structure and is well investigated. This compound shows a and single-chain relaxations and this was investigated on powders but also using single crystals (Rams et al., 2020; Foltyn et al., 2022). The reaction of CoCl2·6H2O, KSeCN with 4-methoxypyridine in water, however, always led to the formation of a compound with the composition Co(NCSe)2(4-methoxypyridine)4 (see Synthesis and crystallization) for which the CN stretching vibration of the anionic ligand is observed at 2068 cm−1, indicative for the presence of only terminally bonded selenocyanate anions (Fig. S1). Even if CoCl2·6H2O and KSeCN were used in excess, no other crystalline phase was obtained. To identify this phase unambiguously, single crystals were grown and characterized by single-crystal X-ray diffraction.
2. Structural commentary
Single-crystal 2(4-methoxypyridine)4, consists of discrete complexes in which the Co cations are sixfold coordinated to four 4-methoxypyridine coligands and two terminal selenocyanate anions that coordinate via the N atom of the anionic ligand to the metal center (Fig. 1). The consists of one CoII cation, two selenocyanate anions and four 4-methoxypyridine ligands in general positions. From the bond lengths and angles, it is obvious that the octahedra are slightly distorted (Table 1). This is also obvious from the angle variance of 1.77 and the quadratic elongation of 1.00 calculated using the method of Robinson (Robinson et al., 1971).
proved that the title compound, Co(NCSe)
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The title compound is isotypic to M(NCS)2(4-methoxypyridine) (M = Co, Fe, Ni) already described in the literature (Mautner et al., 2018; Jochim et al., 2018). In this context, it is noted that Ni(NCS)2(4-methoxypyridine) crystallizes in two polymorphic modifications, of which the form (orthorhombic, Pccn) that is not isotypic to the title compound and M(NCS)2(4-methoxypyridine (M = Co, Fe) represents the thermodynamically stable phase at room temperature (Jochim et al., 2018). However, from this experimental observation one cannot conclude that the title compound is metastable at room temperature and that a second form must exist. It is also noted that the thiocyanate analogs with manganese and cadmium crystallize in a third form (monoclinic, C2/c) and that the Cd(NCS)2 compound also shows dimorphism and additionally crystallizes in a fourth form (tetragonal, P41), which shows the pronounced structural variability for such simple complexes (Jochim et al., 2019). Finally, it is noted that we have not found any evidence that the title compound crystallizes in a further crystalline form.
3. Supramolecular features
In the ) There are a number of intermolecular C—H⋯O and C—H⋯Se contacts, but for most of them the C—H⋯X (X = O, Se) angle is far from linear and the H⋯X distances are too large for any significant interaction (Table 2). Some of C—H⋯Se contacts exhibit angles larger than 150°, which might point to some interaction (Fig. 2 and Table 2).
the discrete complexes are arranged in an irregular manner (Fig. 24. Thermal properties
Based on the single-crystal structural data, a powder pattern was calculated and compared with the experimental pattern, which shows that a pure crystalline phase was obtained (Fig. 3). To investigate if a crystalline ligand deficient phase with the composition Co(NCS)2(4-methoxypyridine)4 can be obtained, measurements using and thermogravimetry with 8°C min−1 were performed. Upon heating, the TG curve shows two poorly resolved mass losses at about 160 and 250°C that are accompanied with endothermic events in the DTA curve (Fig. 4). The DTG curve indicates that the first event consists of two different thermal events that cannot be successfully resolved. Nevertheless, the experimental mass loss was calculated for all three events, which shows that the first mass loss is in reasonable agreement with that calculated for the removal of one 4-methoxypyridine ligand (Δm = −15.5%), whereas the second mass loss points to the removal of two additional 4-methoxypyridine ligands (Fig. 4). This would indicate that in the first step a compound with the composition Co(NCSe)2(4-methoxypyridine)3 is formed, which transforms into Co(NCSe)2(4-methoxypyridine) upon further heating. Compounds with such a ratio between the metal salt and neutral coligands are known for thiocyanate coordination compounds, but are very rare for selenocyanates. One compound with the composition Ni(NCSe)2[N,N′-bis(3-aminopropyl)methylamine]2 is found in which each Ni cation is octahedrally coordinated by three N atoms of one (3-aminopropyl)methylamine ligand plus two bridging and two terminal selenocyanate anions (Vicente et al., 1993). Two of the Ni cations are linked by pairs of μ-1,3-bridging anionic ligands into dinculear units. At first glance, the Ni:coligand ratio seems to be different but one (3-aminopropyl)methylamine ligand replaces three monocoordinating ligands. For a ratio of 1:1 between M(NCS)2 and coligand, no examples can be found with selenocyanate anions but a few examples with thiocyanate are reported in the literature, including Ni(NCS)2(4-aminopyridine), in which Ni(NCS)2 double chains are observed (Neumann et al., 2018).
To increase the resolution, measurements at different heating rates were performed, but the TG curves look similar and are still poorly resolved (Fig. S2). However, to investigate if different crystalline phases can be prepared, the residues obtained at different temperatures were isolated and investigated by PXRD, which proved that they are amorphous, and in Fig. S3 one of these patterns is shown as a representative. We also tried to anneal samples of the title compound at constant temperatures but always obtained amorphous intermediates. Therefore, no more efforts were made.
5. Database survey
In the CCDC database, no selenocyanate compounds with 4-methoxypyridine are reported (CSD version 5.42, last update November 2021; Groom et al., 2016), but some compounds with thiocyanate as the anionic ligand are found. They include compounds with the composition M(NCS)2(4-methoxypyridine)4 with M = Mn (Refcode COBVEX; Jochim et al., 2019), Fe (Refcode FISCIW; Jochim et al., 2018), Co (Refcode KIJPUR; Mautner et al., 2018), Ni (Refcodes FISCAO and FISCES; Jochim et al., 2019), Cd (Refcode COBTUL and COBTUL01; Jochim et al., 2019) and Ru (Refcode NAGPOD; Cadranel et al., 2016), which form discrete complexes with octahedral coordination. All of these compounds crystallize in four different structure types. There are additional discrete octahedral complexes with the composition Cd(NCS)2(4-methoxypyridine)2·4-methoxypyridine (Refcode COBVAT; Jochim et al., 2019) and Ni(NCS)2(4-methoxypyridine)2·acetonitrile (Refcode FISCOC; Jochim et al., 2018) that form solvates and one acetonitrile complex with the composition Ni(NCS)2(4-methoxypyridine)2(CH3CN)2 (Refcode FISCES; Jochim et al., 2018).
With thiocyanate, compounds are reported with the composition M(NCS)2(4-methoxypyridine)2 with M = Cu (Refcode ABOXAT; Handy et al., 2017), Co (KIJQAY, KIJPOL and KIJPOL01; Mautner et al., 2018 and Rams et al., 2020), Ni (FISBUH; Jochim et al., 2018), Cd (COBTUL and COBVIB; Jochim et al., 2019). The Cu compound forms discrete complexes with a square-planar coordination, while the Co compounds consist of isomers forming discrete tetrahedral complexes as well as a chain compound with an octahedral coordination, which is also the case for the Co and Cd compounds.
There are also discrete complexes with selenocyanate anions and pyridine derivatives as coligands reported in the literature that are comparable to the title compound. These include, for example, Fe(NCSe)2[4-2(phenylvinyl)pyridine-N]4 (Refcodes XUKNUN, XUKNUN01, XUKPEZ and XUKPEZ01; Boillot et al., 2009) and Co(NCSe)2 [Refcodes ITISOU (Boeckmann & Näther, 2011) and TIXDOW, TIXDOW01 and TIXFAK (Neumann et al., 2019)].
6. Synthesis and crystallization
CoCl2·6H2O and KSeCN were purchased from Aldrich and 4-methoxypyridine was purchased from Alfa Aesar.
Synthesis:
Larger amounts of a microcrystalline powder were obtained by the reaction of 0.15 mmol (35.7 mg) of CoCl2·6H2O with 0.30 mmol (43.3 mg) of KSeCN and 0.60 mmol (60.8 µL) of 4-methoxypyridine in 1 ml of demineralized water. The mixture was stirred for 2 d at room temperature, the light-pink-colored precipitate was filtered off and washed with a very small amount of water. Single crystals were obtained by slow evaporation of the solvent from the filtrate. It is noted that the same compound is obtained if CoCl2·6H2O and 4-methoxypyridine are used in a 1:1 ratio.
Experimental details:
The XRPD measurements were performed with a Stoe Transmission Powder Diffraction System (STADI P) equipped with a MYTHEN 1K detector and a Johansson-type Ge(111) monochromator using Cu Kα1 radiation (λ = 1.540598 Å). The IR spectra were measured using an ATI Mattson Genesis Series FTIR Spectrometer, control software: WINFIRST, from ATI Mattson. Thermogravimetry and differential thermoanalysis (TG–DTA) measurements were performed in a dynamic nitrogen atmosphere in Al2O3 crucibles using a STA-PT 1000 thermobalance from Linseis. The instrument was calibrated using standard reference materials.
7. Refinement
Crystal data, data collection and structure . Hydrogen atoms were positioned with idealized geometry (C—H = 0.95–0.98 Å, methyl H atoms allowed to rotate but not to tip) and were refined with Uiso(H) = 1.2Ueq(C) (1.5 for methyl H atoms) using a riding model.
details are summarized in Table 3
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Supporting information
CCDC reference: 2242297
https://doi.org/10.1107/S2056989023001391/pk2678sup1.cif
contains datablock I. DOI:Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989023001391/pk2678Isup2.hkl
Fig. S1. IR spectrum of the title compound. Given is the value of the CN stretching vibration of the selenocyanate anions. DOI: https://doi.org/10.1107/S2056989023001391/pk2678sup3.jpg
Fig. S2. Thermogravimetric curves of the title compound at 1, 4 and 8 C/min. DOI: https://doi.org/10.1107/S2056989023001391/pk2678sup4.jpg
Fig. S3. Experimental PXRD pattern of the residue obtained from a TG-DTA measurement of the title compound with 8 C/min at about 240 C. DOI: https://doi.org/10.1107/S2056989023001391/pk2678sup5.jpg
Data collection: X-AREA (Stoe, 2008); cell
X-AREA (Stoe, 2008); data reduction: X-AREA (Stoe, 2008); program(s) used to solve structure: SHELXT2014/5 (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2016/6 (Sheldrick, 2015b); molecular graphics: DIAMOND (Brandenburg & Putz, 1999); software used to prepare material for publication: publCIF (Westrip, 2010).[Co(NCSe)2(C6H7NO)4] | Dx = 1.566 Mg m−3 |
Mr = 705.39 | Mo Kα radiation, λ = 0.71073 Å |
Orthorhombic, Pbca | Cell parameters from 56525 reflections |
a = 10.0531 (2) Å | θ = 1.2–26.0° |
b = 17.3479 (4) Å | µ = 3.05 mm−1 |
c = 34.3141 (5) Å | T = 200 K |
V = 5984.4 (2) Å3 | Block, light pink |
Z = 8 | 0.23 × 0.19 × 0.17 mm |
F(000) = 2824 |
Stoe IPDS-2 diffractometer | 5130 reflections with I > 2σ(I) |
ω scans | Rint = 0.035 |
Absorption correction: numerical (X-Red and X-Shape; Stoe, 2008) | θmax = 26.0°, θmin = 1.2° |
Tmin = 0.457, Tmax = 0.738 | h = −12→9 |
56525 measured reflections | k = −21→21 |
5862 independent reflections | l = −42→42 |
Refinement on F2 | 0 restraints |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.038 | H-atom parameters constrained |
wR(F2) = 0.087 | w = 1/[σ2(Fo2) + (0.0382P)2 + 4.2748P] where P = (Fo2 + 2Fc2)/3 |
S = 1.07 | (Δ/σ)max = 0.003 |
5862 reflections | Δρmax = 0.34 e Å−3 |
356 parameters | Δρmin = −0.47 e Å−3 |
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. |
x | y | z | Uiso*/Ueq | ||
Co1 | 0.42296 (4) | 0.38984 (2) | 0.62207 (2) | 0.04280 (10) | |
N1 | 0.4898 (3) | 0.50081 (14) | 0.60651 (7) | 0.0509 (5) | |
C1 | 0.5320 (3) | 0.56297 (17) | 0.60594 (8) | 0.0479 (6) | |
Se1 | 0.59634 (4) | 0.65844 (2) | 0.60535 (2) | 0.07361 (13) | |
N2 | 0.3601 (2) | 0.27886 (13) | 0.63726 (7) | 0.0504 (5) | |
C2 | 0.3463 (3) | 0.22263 (16) | 0.65509 (8) | 0.0453 (6) | |
Se2 | 0.32769 (4) | 0.13723 (2) | 0.68306 (2) | 0.06769 (12) | |
N11 | 0.3567 (2) | 0.43341 (13) | 0.67705 (6) | 0.0426 (5) | |
C11 | 0.4297 (3) | 0.48409 (16) | 0.69698 (8) | 0.0449 (6) | |
H11 | 0.508929 | 0.502719 | 0.685193 | 0.054* | |
C12 | 0.3978 (3) | 0.51110 (16) | 0.73342 (7) | 0.0435 (6) | |
H12 | 0.454554 | 0.546307 | 0.746578 | 0.052* | |
C13 | 0.2809 (3) | 0.48581 (15) | 0.75052 (8) | 0.0443 (6) | |
C14 | 0.2031 (3) | 0.43319 (16) | 0.72997 (8) | 0.0482 (6) | |
H14 | 0.122509 | 0.414453 | 0.740865 | 0.058* | |
C15 | 0.2436 (3) | 0.40891 (15) | 0.69422 (8) | 0.0449 (6) | |
H15 | 0.189538 | 0.372893 | 0.680651 | 0.054* | |
O11 | 0.2361 (2) | 0.50833 (14) | 0.78569 (6) | 0.0613 (5) | |
C16 | 0.3177 (4) | 0.5600 (2) | 0.80767 (10) | 0.0743 (10) | |
H16A | 0.402605 | 0.534966 | 0.813740 | 0.111* | |
H16B | 0.272280 | 0.573788 | 0.831961 | 0.111* | |
H16C | 0.334262 | 0.606763 | 0.792371 | 0.111* | |
N21 | 0.5040 (2) | 0.34562 (13) | 0.56789 (6) | 0.0469 (5) | |
C21 | 0.5856 (3) | 0.28430 (16) | 0.56790 (8) | 0.0496 (6) | |
H21 | 0.587114 | 0.252310 | 0.590368 | 0.059* | |
C22 | 0.6666 (3) | 0.26539 (16) | 0.53735 (8) | 0.0512 (7) | |
H22 | 0.722378 | 0.221281 | 0.538708 | 0.061* | |
C23 | 0.6661 (3) | 0.31148 (15) | 0.50441 (8) | 0.0475 (6) | |
C24 | 0.5771 (3) | 0.37243 (16) | 0.50266 (8) | 0.0523 (7) | |
H24 | 0.569119 | 0.403015 | 0.479818 | 0.063* | |
C25 | 0.5007 (3) | 0.38721 (17) | 0.53511 (8) | 0.0510 (7) | |
H25 | 0.441604 | 0.429897 | 0.534145 | 0.061* | |
O21 | 0.7538 (2) | 0.29286 (12) | 0.47615 (6) | 0.0593 (5) | |
C26 | 0.7672 (4) | 0.3449 (2) | 0.44407 (10) | 0.0761 (11) | |
H26A | 0.683599 | 0.346536 | 0.429403 | 0.114* | |
H26B | 0.839033 | 0.327220 | 0.426951 | 0.114* | |
H26C | 0.788117 | 0.396546 | 0.453862 | 0.114* | |
N31 | 0.6165 (2) | 0.36451 (13) | 0.64936 (6) | 0.0441 (5) | |
C31 | 0.7328 (3) | 0.38797 (17) | 0.63423 (8) | 0.0513 (7) | |
H31 | 0.730644 | 0.422024 | 0.612555 | 0.062* | |
C32 | 0.8543 (3) | 0.36555 (18) | 0.64827 (9) | 0.0552 (7) | |
H32 | 0.933751 | 0.384252 | 0.636632 | 0.066* | |
C33 | 0.8602 (3) | 0.31539 (17) | 0.67957 (8) | 0.0468 (6) | |
C34 | 0.7418 (3) | 0.29132 (16) | 0.69587 (8) | 0.0478 (6) | |
H34 | 0.741410 | 0.257422 | 0.717608 | 0.057* | |
C35 | 0.6246 (3) | 0.31725 (17) | 0.68008 (7) | 0.0463 (6) | |
H35 | 0.543881 | 0.300535 | 0.691747 | 0.056* | |
O31 | 0.9822 (2) | 0.29425 (13) | 0.69180 (6) | 0.0613 (5) | |
C36 | 0.9907 (4) | 0.2312 (2) | 0.71856 (11) | 0.0772 (10) | |
H36A | 0.949864 | 0.245955 | 0.743396 | 0.116* | |
H36B | 1.084362 | 0.217962 | 0.722851 | 0.116* | |
H36C | 0.943834 | 0.186517 | 0.707773 | 0.116* | |
N41 | 0.2300 (2) | 0.41270 (13) | 0.59591 (6) | 0.0471 (5) | |
C41 | 0.1720 (3) | 0.36068 (17) | 0.57240 (9) | 0.0562 (7) | |
H41 | 0.214155 | 0.312096 | 0.569187 | 0.067* | |
C42 | 0.0557 (3) | 0.37370 (19) | 0.55288 (9) | 0.0592 (8) | |
H42 | 0.019107 | 0.335190 | 0.536376 | 0.071* | |
C43 | −0.0080 (3) | 0.44397 (18) | 0.55750 (8) | 0.0512 (6) | |
C44 | 0.0467 (3) | 0.49680 (16) | 0.58295 (8) | 0.0505 (7) | |
H44 | 0.003580 | 0.544520 | 0.587894 | 0.061* | |
C45 | 0.1652 (3) | 0.47896 (15) | 0.60105 (8) | 0.0476 (6) | |
H45 | 0.202896 | 0.516039 | 0.618178 | 0.057* | |
O41 | −0.1208 (2) | 0.45430 (15) | 0.53667 (7) | 0.0696 (6) | |
C46 | −0.1853 (4) | 0.5276 (2) | 0.53937 (13) | 0.0798 (11) | |
H46A | −0.212437 | 0.536910 | 0.566395 | 0.120* | |
H46B | −0.263923 | 0.528030 | 0.522492 | 0.120* | |
H46C | −0.123661 | 0.568224 | 0.531068 | 0.120* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Co1 | 0.04374 (19) | 0.04212 (19) | 0.04252 (19) | −0.00171 (15) | 0.00192 (15) | 0.00372 (14) |
N1 | 0.0553 (14) | 0.0453 (13) | 0.0522 (13) | −0.0025 (11) | 0.0056 (11) | 0.0050 (10) |
C1 | 0.0508 (16) | 0.0524 (16) | 0.0405 (13) | 0.0026 (13) | 0.0043 (12) | 0.0047 (11) |
Se1 | 0.0947 (3) | 0.05033 (18) | 0.0758 (2) | −0.02052 (18) | 0.00388 (19) | 0.00265 (15) |
N2 | 0.0518 (14) | 0.0460 (13) | 0.0532 (13) | −0.0049 (11) | −0.0007 (11) | 0.0044 (11) |
C2 | 0.0431 (14) | 0.0463 (15) | 0.0465 (14) | −0.0031 (12) | −0.0012 (11) | −0.0067 (12) |
Se2 | 0.0820 (3) | 0.04693 (18) | 0.0741 (2) | −0.00859 (16) | −0.00418 (18) | 0.01474 (15) |
N11 | 0.0373 (11) | 0.0470 (12) | 0.0435 (11) | −0.0019 (9) | 0.0011 (9) | 0.0020 (9) |
C11 | 0.0371 (13) | 0.0513 (15) | 0.0463 (14) | −0.0056 (11) | 0.0006 (11) | 0.0047 (11) |
C12 | 0.0393 (14) | 0.0477 (14) | 0.0436 (13) | −0.0030 (11) | −0.0023 (11) | 0.0031 (11) |
C13 | 0.0431 (14) | 0.0473 (14) | 0.0426 (13) | 0.0031 (12) | 0.0030 (11) | 0.0028 (11) |
C14 | 0.0386 (14) | 0.0539 (16) | 0.0523 (15) | −0.0053 (12) | 0.0053 (12) | 0.0034 (12) |
C15 | 0.0377 (13) | 0.0459 (14) | 0.0511 (14) | −0.0042 (11) | 0.0014 (11) | 0.0028 (11) |
O11 | 0.0571 (12) | 0.0760 (14) | 0.0509 (11) | −0.0092 (11) | 0.0127 (10) | −0.0123 (10) |
C16 | 0.082 (2) | 0.082 (2) | 0.0585 (19) | −0.018 (2) | 0.0122 (17) | −0.0227 (17) |
N21 | 0.0525 (14) | 0.0458 (12) | 0.0424 (11) | 0.0030 (10) | 0.0003 (10) | 0.0025 (9) |
C21 | 0.0608 (17) | 0.0426 (14) | 0.0452 (14) | 0.0043 (13) | 0.0002 (12) | 0.0034 (11) |
C22 | 0.0617 (18) | 0.0419 (14) | 0.0499 (15) | 0.0077 (13) | −0.0003 (13) | −0.0001 (12) |
C23 | 0.0534 (16) | 0.0433 (14) | 0.0457 (14) | −0.0035 (12) | 0.0041 (12) | −0.0052 (11) |
C24 | 0.0649 (18) | 0.0483 (15) | 0.0436 (14) | 0.0069 (13) | −0.0003 (13) | 0.0044 (12) |
C25 | 0.0568 (17) | 0.0528 (16) | 0.0434 (14) | 0.0098 (13) | −0.0011 (13) | 0.0033 (12) |
O21 | 0.0743 (14) | 0.0504 (11) | 0.0532 (11) | 0.0053 (10) | 0.0172 (10) | −0.0017 (9) |
C26 | 0.101 (3) | 0.0597 (19) | 0.067 (2) | 0.0058 (19) | 0.035 (2) | 0.0068 (16) |
N31 | 0.0420 (12) | 0.0459 (12) | 0.0445 (11) | −0.0011 (10) | 0.0022 (9) | 0.0036 (9) |
C31 | 0.0481 (16) | 0.0540 (16) | 0.0520 (15) | −0.0062 (13) | 0.0044 (12) | 0.0114 (13) |
C32 | 0.0437 (15) | 0.0617 (18) | 0.0601 (17) | −0.0075 (14) | 0.0074 (13) | 0.0104 (14) |
C33 | 0.0404 (14) | 0.0499 (15) | 0.0501 (14) | −0.0031 (12) | −0.0030 (12) | −0.0017 (12) |
C34 | 0.0472 (15) | 0.0512 (15) | 0.0450 (14) | −0.0061 (12) | −0.0002 (12) | 0.0063 (12) |
C35 | 0.0415 (14) | 0.0542 (15) | 0.0432 (13) | −0.0051 (12) | 0.0035 (11) | 0.0063 (12) |
O31 | 0.0428 (11) | 0.0712 (14) | 0.0700 (13) | −0.0044 (10) | −0.0064 (10) | 0.0116 (11) |
C36 | 0.058 (2) | 0.090 (3) | 0.084 (2) | 0.0044 (19) | −0.0175 (18) | 0.027 (2) |
N41 | 0.0496 (13) | 0.0450 (12) | 0.0466 (12) | 0.0013 (10) | −0.0008 (10) | 0.0004 (9) |
C41 | 0.0558 (18) | 0.0505 (16) | 0.0623 (17) | 0.0076 (14) | −0.0092 (14) | −0.0121 (13) |
C42 | 0.0569 (18) | 0.0586 (18) | 0.0620 (18) | 0.0030 (14) | −0.0083 (14) | −0.0128 (14) |
C43 | 0.0437 (15) | 0.0586 (17) | 0.0513 (15) | 0.0013 (13) | 0.0005 (12) | 0.0066 (13) |
C44 | 0.0502 (16) | 0.0450 (14) | 0.0563 (16) | 0.0032 (12) | 0.0064 (13) | 0.0053 (12) |
C45 | 0.0524 (16) | 0.0408 (13) | 0.0494 (15) | −0.0002 (12) | 0.0019 (12) | 0.0016 (11) |
O41 | 0.0531 (13) | 0.0749 (15) | 0.0807 (15) | 0.0082 (12) | −0.0151 (11) | 0.0034 (12) |
C46 | 0.061 (2) | 0.076 (2) | 0.102 (3) | 0.0171 (18) | −0.013 (2) | 0.017 (2) |
Co1—N2 | 2.092 (2) | C25—H25 | 0.9500 |
Co1—N1 | 2.108 (2) | O21—C26 | 1.430 (4) |
Co1—N11 | 2.139 (2) | C26—H26A | 0.9800 |
Co1—N21 | 2.170 (2) | C26—H26B | 0.9800 |
Co1—N41 | 2.174 (2) | C26—H26C | 0.9800 |
Co1—N31 | 2.203 (2) | N31—C35 | 1.338 (3) |
N1—C1 | 1.159 (4) | N31—C31 | 1.342 (4) |
C1—Se1 | 1.778 (3) | C31—C32 | 1.370 (4) |
N2—C2 | 1.160 (3) | C31—H31 | 0.9500 |
C2—Se2 | 1.775 (3) | C32—C33 | 1.384 (4) |
N11—C11 | 1.334 (3) | C32—H32 | 0.9500 |
N11—C15 | 1.349 (3) | C33—O31 | 1.347 (3) |
C11—C12 | 1.373 (4) | C33—C34 | 1.379 (4) |
C11—H11 | 0.9500 | C34—C35 | 1.373 (4) |
C12—C13 | 1.384 (4) | C34—H34 | 0.9500 |
C12—H12 | 0.9500 | C35—H35 | 0.9500 |
C13—O11 | 1.346 (3) | O31—C36 | 1.431 (4) |
C13—C14 | 1.393 (4) | C36—H36A | 0.9800 |
C14—C15 | 1.359 (4) | C36—H36B | 0.9800 |
C14—H14 | 0.9500 | C36—H36C | 0.9800 |
C15—H15 | 0.9500 | N41—C45 | 1.333 (3) |
O11—C16 | 1.431 (4) | N41—C41 | 1.344 (4) |
C16—H16A | 0.9800 | C41—C42 | 1.366 (4) |
C16—H16B | 0.9800 | C41—H41 | 0.9500 |
C16—H16C | 0.9800 | C42—C43 | 1.386 (4) |
N21—C25 | 1.337 (3) | C42—H42 | 0.9500 |
N21—C21 | 1.343 (3) | C43—O41 | 1.353 (3) |
C21—C22 | 1.367 (4) | C43—C44 | 1.380 (4) |
C21—H21 | 0.9500 | C44—C45 | 1.379 (4) |
C22—C23 | 1.384 (4) | C44—H44 | 0.9500 |
C22—H22 | 0.9500 | C45—H45 | 0.9500 |
C23—O21 | 1.350 (3) | O41—C46 | 1.431 (4) |
C23—C24 | 1.386 (4) | C46—H46A | 0.9800 |
C24—C25 | 1.377 (4) | C46—H46B | 0.9800 |
C24—H24 | 0.9500 | C46—H46C | 0.9800 |
N2—Co1—N1 | 178.93 (10) | N21—C25—H25 | 117.8 |
N2—Co1—N11 | 90.65 (9) | C24—C25—H25 | 117.8 |
N1—Co1—N11 | 90.00 (9) | C23—O21—C26 | 117.6 (2) |
N2—Co1—N21 | 90.08 (9) | O21—C26—H26A | 109.5 |
N1—Co1—N21 | 89.20 (9) | O21—C26—H26B | 109.5 |
N11—Co1—N21 | 176.06 (9) | H26A—C26—H26B | 109.5 |
N2—Co1—N41 | 90.07 (9) | O21—C26—H26C | 109.5 |
N1—Co1—N41 | 90.76 (9) | H26A—C26—H26C | 109.5 |
N11—Co1—N41 | 91.26 (8) | H26B—C26—H26C | 109.5 |
N21—Co1—N41 | 92.61 (9) | C35—N31—C31 | 115.9 (2) |
N2—Co1—N31 | 88.71 (9) | C35—N31—Co1 | 120.72 (18) |
N1—Co1—N31 | 90.47 (9) | C31—N31—Co1 | 122.96 (18) |
N11—Co1—N31 | 88.32 (8) | N31—C31—C32 | 123.7 (3) |
N21—Co1—N31 | 87.83 (9) | N31—C31—H31 | 118.2 |
N41—Co1—N31 | 178.70 (9) | C32—C31—H31 | 118.2 |
C1—N1—Co1 | 166.1 (2) | C31—C32—C33 | 119.3 (3) |
N1—C1—Se1 | 179.7 (3) | C31—C32—H32 | 120.3 |
C2—N2—Co1 | 160.3 (2) | C33—C32—H32 | 120.3 |
N2—C2—Se2 | 178.8 (3) | O31—C33—C34 | 125.2 (3) |
C11—N11—C15 | 116.6 (2) | O31—C33—C32 | 116.9 (3) |
C11—N11—Co1 | 120.90 (17) | C34—C33—C32 | 117.9 (3) |
C15—N11—Co1 | 122.44 (18) | C35—C34—C33 | 118.8 (2) |
N11—C11—C12 | 124.3 (2) | C35—C34—H34 | 120.6 |
N11—C11—H11 | 117.9 | C33—C34—H34 | 120.6 |
C12—C11—H11 | 117.9 | N31—C35—C34 | 124.3 (3) |
C11—C12—C13 | 118.4 (2) | N31—C35—H35 | 117.8 |
C11—C12—H12 | 120.8 | C34—C35—H35 | 117.8 |
C13—C12—H12 | 120.8 | C33—O31—C36 | 117.6 (2) |
O11—C13—C12 | 124.9 (3) | O31—C36—H36A | 109.5 |
O11—C13—C14 | 117.1 (2) | O31—C36—H36B | 109.5 |
C12—C13—C14 | 118.0 (2) | H36A—C36—H36B | 109.5 |
C15—C14—C13 | 119.4 (2) | O31—C36—H36C | 109.5 |
C15—C14—H14 | 120.3 | H36A—C36—H36C | 109.5 |
C13—C14—H14 | 120.3 | H36B—C36—H36C | 109.5 |
N11—C15—C14 | 123.3 (3) | C45—N41—C41 | 116.5 (2) |
N11—C15—H15 | 118.4 | C45—N41—Co1 | 122.59 (19) |
C14—C15—H15 | 118.4 | C41—N41—Co1 | 120.87 (19) |
C13—O11—C16 | 117.5 (2) | N41—C41—C42 | 123.7 (3) |
O11—C16—H16A | 109.5 | N41—C41—H41 | 118.1 |
O11—C16—H16B | 109.5 | C42—C41—H41 | 118.1 |
H16A—C16—H16B | 109.5 | C41—C42—C43 | 119.0 (3) |
O11—C16—H16C | 109.5 | C41—C42—H42 | 120.5 |
H16A—C16—H16C | 109.5 | C43—C42—H42 | 120.5 |
H16B—C16—H16C | 109.5 | O41—C43—C44 | 125.5 (3) |
C25—N21—C21 | 116.3 (2) | O41—C43—C42 | 116.3 (3) |
C25—N21—Co1 | 121.38 (19) | C44—C43—C42 | 118.2 (3) |
C21—N21—Co1 | 120.60 (18) | C45—C44—C43 | 118.7 (3) |
N21—C21—C22 | 123.6 (3) | C45—C44—H44 | 120.6 |
N21—C21—H21 | 118.2 | C43—C44—H44 | 120.6 |
C22—C21—H21 | 118.2 | N41—C45—C44 | 123.8 (3) |
C21—C22—C23 | 119.0 (3) | N41—C45—H45 | 118.1 |
C21—C22—H22 | 120.5 | C44—C45—H45 | 118.1 |
C23—C22—H22 | 120.5 | C43—O41—C46 | 117.6 (3) |
O21—C23—C22 | 116.5 (3) | O41—C46—H46A | 109.5 |
O21—C23—C24 | 125.0 (3) | O41—C46—H46B | 109.5 |
C22—C23—C24 | 118.6 (3) | H46A—C46—H46B | 109.5 |
C25—C24—C23 | 117.8 (3) | O41—C46—H46C | 109.5 |
C25—C24—H24 | 121.1 | H46A—C46—H46C | 109.5 |
C23—C24—H24 | 121.1 | H46B—C46—H46C | 109.5 |
N21—C25—C24 | 124.5 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
C11—H11···O11i | 0.95 | 2.49 | 3.165 (3) | 128 |
C15—H15···O31ii | 0.95 | 2.52 | 3.297 (3) | 139 |
C16—H16B···Se1iii | 0.98 | 3.15 | 4.096 (3) | 163 |
C22—H22···Se1iv | 0.95 | 3.12 | 3.817 (3) | 132 |
C26—H26A···Se1v | 0.98 | 3.06 | 4.029 (5) | 171 |
C36—H36B···Se2vi | 0.98 | 3.13 | 3.952 (4) | 142 |
C41—H41···O21vii | 0.95 | 2.43 | 3.248 (4) | 144 |
C45—H45···Se2viii | 0.95 | 3.08 | 3.932 (3) | 151 |
C46—H46A···Se1ii | 0.98 | 3.15 | 3.885 (4) | 133 |
Symmetry codes: (i) x+1/2, y, −z+3/2; (ii) x−1, y, z; (iii) x−1/2, y, −z+3/2; (iv) −x+3/2, y−1/2, z; (v) −x+1, −y+1, −z+1; (vi) x+1, y, z; (vii) x−1/2, −y+1/2, −z+1; (viii) −x+1/2, y+1/2, z. |
Acknowledgements
This work was supported by the State of Schleswig-Holstein.
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