Crystals (Apr 2016)

Synthesis, Structures and Properties of Cobalt Thiocyanate Coordination Compounds with 4-(hydroxymethyl)pyridine as Co-ligand

  • Stefan Suckert,
  • Luzia S. Germann,
  • Robert E. Dinnebier,
  • Julia Werner,
  • Christian Näther

DOI
https://doi.org/10.3390/cryst6040038
Journal volume & issue
Vol. 6, no. 4
p. 38

Abstract

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Reaction of Co(NCS)2 with 4-(hydroxymethyl)pyridine (hmpy) leads to the formation of six new coordination compounds with the composition [Co(NCS)2(hmpy))4] (1), [Co(NCS)2(hmpy)4] × H2O (1-H2O), [Co(NCS)2(hmpy)2(EtOH)2] (2), [Co(NCS)2(hmpy)2(H2O)2] (3), [Co(NCS)2(hmpy)2]n∙4 H2O (4) and [Co(NCS)2(hmpy)2]n (5). They were characterized by single crystal and powder X-ray diffraction experiments, thermal and elemental analysis, IR and magnetic measurements. Compound 1 and 1-H2O form discrete complexes, in which the Co(II) cations are octahedrally coordinated by two terminal thiocyanato anions and four 4-(hydroxymethyl)pyridine ligands. Discrete complexes were also observed for compounds 2 and 3 where two of the hmpy ligands were substituted by solvent, either water (3) or ethanol (2). In contrast, in compounds 4 and 5, the Co(II) cations are linked into chains by bridging 4-(hydroxymethyl)pyridine ligands. The phase purity was checked with X-ray powder diffraction. Thermogravimetric measurements showed that compound 3 transforms into 5 upon heating, whereas the back transformation occurs upon resolvation. Magnetic measurements did not show any magnetic exchange via the hmpy ligand for compound 5.

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