Issue 42, 2007

Dinuclear zinc(ii) complexes of symmetric Schiff-base ligands with extended quinoline sidearms

Abstract

The synthesis of two 2-formylquinolines is reported via the Skraup method followed by SeO2 oxidation. Each aldehyde is condensed with (1R,2R)-diaminocyclohexane and (R)-BINAM, yielding four enantiomerically-pure bis(imine–quinoline) ligands. The neutral ligands are reacted with ZnCl2 to give complexes with bis(bidentate) coordination of ZnCl2 units. X-Ray structural characterization of three complexes shows them to have a single-stranded helical motif, with M helicity, except in one case where a 1 : 1 mixture of M and P helices is seen. The ligands and complexes are further characterized spectroscopically by solution 1H and 13C NMR, UV-vis and ECD.

Graphical abstract: Dinuclear zinc(ii) complexes of symmetric Schiff-base ligands with extended quinoline sidearms

Supplementary files

Article information

Article type
Paper
Submitted
21 Jun 2007
Accepted
27 Jul 2007
First published
29 Aug 2007

Dalton Trans., 2007, 4788-4796

Dinuclear zinc(II) complexes of symmetric Schiff-base ligands with extended quinoline sidearms

D. Prema, A. V. Wiznycia, B. M. T. Scott, J. Hilborn, J. Desper and C. J. Levy, Dalton Trans., 2007, 4788 DOI: 10.1039/B709454J

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