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Copper N2S2 Schiff base macrocycles: the effect of structure on redox potential

Taylor, M.K. and Trotter, Katherine D. and Reglinski, J. and Berlouis, L. and Kennedy, A.R. and Spickett, C.M. and Sowden, Rebecca J. (2008) Copper N2S2 Schiff base macrocycles: the effect of structure on redox potential. Inorganica Chimica Acta, 361 (9-10). pp. 2851-2862. ISSN 0020-1693

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Abstract

A series of bis-salicylidene based N2S2 copper macrocycles were prepared, structurally characterised and subjected to electrochemical analysis. The aim was to investigate the effects of length of polymethylene chains between either the imine donors or the sulfur donors on redox state and potential of the metal. The complexes structurally characterised had either distorted square planar or tetrahedral geometries depending on their oxidation state (Cu2+ or Cu+, respectively), and the N-(CH2)n-N bridge was found to be most critical moiety in determining the redox potential and oxidation state of the copper macrocycles, with relatively little change in these properties caused by lengthening the S-(CH2)n-S bridge from two to three carbons. In fact, a weakness was observed in the complexes at the sulfur donor, as further lengthening of the S-(CH2)n-S methylene bridge to four carbons caused fission of the carbon-sulfur bond to give dimeric rings and supramolecular assemblies. Cu+ complexes could be oxidised to Cu2+ by tert-butylhydroperoxide, with a corresponding change in the spectrophotometric properties, and likewise Cu2+ complexes could be reduced to Cu+ by treatment with β-mercaptoethylamine. However, repeated redox cycles appeared to compromise the stability of the macrocycles, most probably by a competing oxidation of the ligand. Thus the copper N2S2 macrocycles show potential as redox sensors, but further development is required to improve their performance in a biochemical environment.

Item type: Article
ID code: 15987
Keywords: macrocycle, copper, redox potential, geometry, donor groups, Therapeutics. Pharmacology, Pharmacy and materia medica, Microbiology, Materials Chemistry, Physical and Theoretical Chemistry, Inorganic Chemistry
Subjects: Medicine > Therapeutics. Pharmacology
Medicine > Pharmacy and materia medica
Science > Microbiology
Department: Faculty of Science > Pure and Applied Chemistry
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Related URLs:
    Depositing user: Ms Ann Barker-Myles
    Date Deposited: 16 Feb 2010 15:07
    Last modified: 04 Sep 2014 22:49
    URI: http://strathprints.strath.ac.uk/id/eprint/15987

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