Issue 24, 2003

A facile route to hetero-bimetallic Ti(iv)-alkali metal calix[4]arene complexes

Abstract

Deprotonation of calix[4]arenes by alkali metal in methanol using simple benchtop procedures is effective in the formation of novel monomeric and dimeric titanium(IV) complexes. For the larger alkali metal cations, K+ and Cs+, favourable complexation within the π-basic calix[4]arene cavity facilitates the formation of monomeric titanium(IV) complexes when oligomer formation is inhibited by an acetylacetonate ligand. In contrast, the smaller Li+ and Na+ ions preferentially form dimeric complexes with exo-bridging alkali and titanium(IV) metal centres. A dimeric complex is also obtained for potassium in the absence of acetylacetonate. The solid state structures of the K–Ti and Na–Ti calix[4]arene dimer complexes show different structural characteristics depending on the nature of the alkali metal.

Graphical abstract: A facile route to hetero-bimetallic Ti(iv)-alkali metal calix[4]arene complexes

Supplementary files

Article information

Article type
Paper
Submitted
02 Sep 2003
Accepted
22 Oct 2003
First published
05 Nov 2003

Dalton Trans., 2003, 4590-4597

A facile route to hetero-bimetallic Ti(IV)-alkali metal calix[4]arene complexes

A. J. Petrella, D. C. Craig, R. N. Lamb, C. L. Raston and N. K. Roberts, Dalton Trans., 2003, 4590 DOI: 10.1039/B310635G

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