Article ID Journal Published Year Pages File Type
1307600 Inorganica Chimica Acta 2008 5 Pages PDF
Abstract

A fast two-step synthetic approach for 4,4′-thioacetyl-functionalised 2,2′-bipyridine is described. Ethylcarbamoyl groups are used as spacers between the sulfur atoms and the pyridyl rings. Both reactions proceed in a highly selective manner. The coordinating properties of the ligand have been assessed.

Graphical abstractA rapid synthetic procedure has been devised for the preparation of a doubly thioacetyl-functionalised bipyridine-based ligand which involves the transformation of 4,4′-dimethyl-2,2′-bipyridine into an activated diester whose electrophilicity shows high amine over thiol preference. Subsequent reaction with appropriate transition metal precursors afforded both homo- and heteroleptic tris(bipyridine)-type octahedral complexes.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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