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Complexation and proton transfer by hydroxamic acids in model inhibited metallohydrolases: formation of metal hydroxamate trimers

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UNSPECIFIED. (2004) Complexation and proton transfer by hydroxamic acids in model inhibited metallohydrolases: formation of metal hydroxamate trimers. INORGANIC CHEMISTRY COMMUNICATIONS, 7 (4). pp. 495-498. ISSN 1387-7003

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/j.inoche.2003.12.038

Abstract

Reaction between the dimeric metal complexes, [M-2(mu-OAcF)(2) (OAcF)(2) (mu-H2O)(tmen)(2)], M = Co(II), Ni(II), and aceto- and benzohydroxamic acids (AHA, BHA) gives the novel trimeric complexes, [M-3(mu-OAcF)(4)(mu-RA)(2)(tmen)(2)], M=Co(II), Ni(II); RA = AA, BA, in which each hydroxamate bridges two metal centres via its deprotonated hydroxyl and the carbonyl oxygen bonds one metal centre only together with the doubly protonated salt [(tmen).2H][OAcF](2). In contrast, self-assembly from M(OAcF)(2).4H(2)O, tmen and RHA gives the dibridged hydroxamate dimers [M-2(mu-OAcF)(mu-RA)(2)(tmen)(2)] [OAcF]. (C) 2004 Elsevier B.V. All rights reserved.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: INORGANIC CHEMISTRY COMMUNICATIONS
Publisher: ELSEVIER SCIENCE BV
ISSN: 1387-7003
Date: April 2004
Volume: 7
Number: 4
Number of Pages: 4
Page Range: pp. 495-498
Identification Number: 10.1016/j.inoche.2003.12.038
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/8577

Data sourced from Thomson Reuters' Web of Knowledge

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