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Optically induced valence tautomeric interconversion in cobalt dioxolene complexes

Journal

JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
Volume 17, Issue 8, Pages 1522-1533

Publisher

SOC BRASILEIRA QUIMICA
DOI: 10.1590/S0103-50532006000800007

Keywords

valence tautomerism; redox isomerism; photochromism; photoinduction; photomagnetism; semiquinone; radical ligand

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The discovery that a number of cobalt-dioxolene complexes undergo photoswitchable behavior was reported in the recent past. This phenomenon is always associated with valence tautomeric interconversion processes involving low-spin cobalt(III) and high-spin cobalt(II) species. Herein is stressed the strong formal correlation existing between these processes and the LIESST (Light-Induced Excited Spin State Trapping) effect shown by several iron( II) complexes undergoing spin crossover interconversion. The dynamics of the relaxation of the photoinduced metastable species to the ground state is discussed in terms of non-adiabatic processes within the Jortner theory of radiationless multiphonon relaxation.

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