Summary
Crystalline copper(I) complexes of the general formula [LCuCl] and [L2CuCl] were prepared for imidazolidine-2-thiones and 1,3-diazinane-2-thiones by the reduction of copper(II) halides with an excess of the ligands. The13C n.m.r. and i.r. spectra of these complexes are consistent with thione sulphur (ligand) donation in all cases. The magnitude of the high-field shift in the13C resonance of the thioureide carbon in the complexes as compared with that of the free ligands is interpreted in terms of coordination geometry around the metal atoms. A comparison of the chemical shifts for gold(I), silver(I) and copper(I) revealed a displacement ofca. 6–8 ppm for the mono- and 2–4 ppm for the bis-complexes, respectively.
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Isab, A.A., Hussain, M.S. Carbon-13 N.m.r. and I.r. Studies of copper(I) complexes of the — NHCS group in five- and six-membered heterocyclic rings. Transition Met Chem 11, 298–301 (1986). https://doi.org/10.1007/BF00620651
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DOI: https://doi.org/10.1007/BF00620651