Issue 9, 1996

Face versus vertex co-ordination of tridentate crown thioethers to trinuclear cobalt clusters

Abstract

The co-ordination of the six-membered crown thioethers 1,3,5-trithiane, 2-methyl-, 2,4-dimethyl-, 2,4,6-trimethyl-, 2-benzyl- and 2,4,6-tribenzyl-1,3,5-trithiane and the nine-membered crown thioether 1,4,7-trithiacyclononane to the cobalt skeleton of various Co3C clusters was studied. With trithiane and its derivatives complexes of the type [Co3(CO)63-SCHR1SCHR2SCHR3)](R = Cl, Me or Ph; R1– R3= H, Me or CH2Ph) were obtained, whereas the nine-membered crown thioether gave compounds of the type [Co3(CO)5(µ-CO)(µ3-CR){(SCH2CH2)3}]. The molecular and crystal structures of several representatives have been investigated by single-crystal X-ray diffraction. It has been shown that the trithiane ligand invariably occupies the axial co-ordination sites on the three cobalt atoms, while the trithiacyclononane chelates on one cobalt atom. The intermolecular networks of hydrogen-bonding interactions of the C–H ⋯ O type between the thioether hydrogens and the CO ligands have been investigated and compared with those present in other crystalline clusters carrying thioether ligands.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1996, 1875-1883

Face versus vertex co-ordination of tridentate crown thioethers to trinuclear cobalt clusters

C. Renouard, G. Rheinwald, H. Stoeckli-Evans, G. Süss-Fink, D. Braga and F. Grepioni, J. Chem. Soc., Dalton Trans., 1996, 1875 DOI: 10.1039/DT9960001875

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