Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 345713
Title Electronic structure of transition metal-isocorrole complexes: a first quantum chemical study
Author(s) Oort, B.F. van; Tangen, E.; Ghosh, A.
Source European Journal of Inorganic Chemistry 2004 (2004)12. - ISSN 1434-1948 - p. 2442 - 2445.
Department(s) Biophysics
Publication type Refereed Article in a scientific journal
Publication year 2004
Keyword(s) peroxidase compound-i - pi-cation radicals - noninnocent ligands - porphyrins - corroles - centers - iron(iv) - electrochemistry - absorption - insights
Abstract DFT calculations indicate that the broad electronic-structural features of metalloisocorroles are rather similar to those of analogous metallocorroles. Thus, like their corrole analogues, many metalloisocorroles feature substantially non-innocent ligands. Another key point is that both corroles and isocorroles can exhibit at least two kinds of radical character, a2 and b1. However, corrole and isocorrole derivatives also differ significantly in a few ways: for example, the S = 1/2 CoPh complexes of corrole and isocorrole exhibit ground states of different symmetries (2A and 2A, respectively, in Cs notation), reflecting different interplays of metal(d)-ligand(p) interactions in corrole versus isocorrole derivatives. The ligand non-innocence phenomena encountered in this study are broadly reminiscent of similar phenomena in peroxidase compound I intermediates and their synthetic models. It seems reasonable, therefore, to adopt the view that this study, along with related studies on corrole derivatives, provides a broader chemical context for appreciating the electronic structures of high-valent heme protein intermediates.
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