Abstract

Heterocyclic thioamides react with Os 3(CO) 10(MeCN) 2 to yield complexes HOs 3(CO) 10L of the deprotonated thioamide coordinated in the thiolate form via the exocyclic sulphur atom. Decarbonylation yields HOS 3(CO) 9L with L coordinated via both sulphur and nitrogen: these can be desulphurised to yield sulphur-capped cluster species.

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