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- Title
Synthesis, crystal structure and properties of Cd(NCS)<sub>2</sub> coordination compounds with two different Cd coordination modes.
- Authors
Jochim, Aleksej; Gallo, Gianpiero; Dinnebier, Robert; Näther, Christian
- Abstract
Reaction of Cd(NCS)2 with 4-methoxypyridine leads to the formation of four new compounds, of which one crystallizes in two different polymorphs. In Cd(NCS)2(4-methoxypyridine)4·(4-methoxypyridine)2 (1) and Cd(NCS)2(4-methoxypyridine)4 (2-I and 2-II) discrete complexes are found, in which the Cd cations are octahedrally coordinated by four 4-methoxypyridine co-ligands and two terminally N-bonded thiocyanate anions. For the polymorphs 2-I and 2-II no single crystals are available and therefore, the corresponding Mn(II) compound (2-I-Mn) was prepared, which is isotypic to 2-I, as proven by a Rietveld refinement. The crystal structure of 2-II was solved and refined from XRPD data. In [Cd(NCS)2(4-methoxypyridine)2]n (3), the Cd cations are also octahedrally coordinated but linked into linear chains by pairs of thiocyanate anions with all ligands in trans-position. {[Cd(NCS)2]3(4-methoxypyridine)5}n (4) also consists of chains but two different Cd coordination modes are observed. Two of the three crystallographically independent Cd cations show an octahedral coordination with a trans- or cis-arrangement of the N and S atoms of the anionic ligands, whereas the third one is in a distorted square-pyramidal coordination, with cis-coordination of the thiocyanate N and S atoms. Measurements using simultaneous thermogravimetry and differential scanning calorimetry of 2-I and 2-II show different heating rate dependent mass steps, in which the co-ligands are removed. In some of the residues obtained after the respective TG steps compound 3 was detected but no phase pure samples could be obtained.
- Subjects
X-ray diffraction; CRYSTAL structure; THERMOGRAVIMETRY; GRAVIMETRIC analysis; INORGANIC compounds
- Publication
Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2019, Vol 74, Issue 1, p49
- ISSN
0932-0776
- Publication type
Article
- DOI
10.1515/znb-2018-0169