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Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand†
Chui-Shan Tsang,Ho-Lun Yeung,Wing-Tak Wong,Hoi-Lun Kwong
Chemical Communications Pub Date : 02/25/2009 00:00:00 , DOI:10.1039/B900264B
Abstract

Reaction of a pinene-based pyridylthioamide with 1,4-dibromo-2,3-butanedione in refluxing methanol yielded a new chiral pyridylthiazole ligand L which forms a dinuclear double-stranded helicate with Cu(I) ions; this helicate has opposite helical chirality when compared with its quaterpyridine analogue.

Graphical abstract: Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand
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