Reactivity difference between protolytic forms of some macrocyclic chromium(III) complexes in ligand substitution and electron transfer processes

A. Katafias, J. Chatlas, O. Impert, P. Kita, E. Madej, A. Topolski, G. Wrzeszcz, J. Eriksen, O. Monsted, A. Mills

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

The review provides insight into the mechanism of ligand substitution and electron transfer (from chromium(III) to iron(III)) by comparison of the reactivity of some tetraazamacrocyclic chromium(III) complexes in the conjugate acid-base forms. Use of two geometrical isomers made possible to estimate the influence of geometry and protolytic reactions in trans and cis position towards the leaving group on the rate enhancement. Studies on the reaction rates in different media demonstrated the role played by outer sphere interactions in a monodentate ligand substitution. (C) 2009 Published by Elsevier B.V.
Original languageEnglish
Pages (from-to)2346-2356, Impact Factor: 2.0
Number of pages11
JournalInorganica Chimica Acta
Volume363
DOIs
Publication statusPublished - 2010

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Physical and Theoretical Chemistry
  • Materials Chemistry

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