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Structure and Reactivity Studies on Dinuclear Copper Complexes of the Ligand α,α′-Bis{bis[1-(1′-methyl-2′-benzimidazolyl)methyl]amino}-m-xylene
European journal of inorganic chemistry, 2003-03, Vol.2003 (6), p.1197-1205
Battaini, Giuseppe
Casella, Luigi
Gullotti, Michele
Monzani, Enrico
Nardin, Giorgio
Perotti, Angelo
Randaccio, Lucio
Santagostini, Laura
Heinemann, Frank W.
Schindler, Siegfried
2003
Details
Autor(en) / Beteiligte
Battaini, Giuseppe
Casella, Luigi
Gullotti, Michele
Monzani, Enrico
Nardin, Giorgio
Perotti, Angelo
Randaccio, Lucio
Santagostini, Laura
Heinemann, Frank W.
Schindler, Siegfried
Titel
Structure and Reactivity Studies on Dinuclear Copper Complexes of the Ligand α,α′-Bis{bis[1-(1′-methyl-2′-benzimidazolyl)methyl]amino}-m-xylene
Ist Teil von
European journal of inorganic chemistry, 2003-03, Vol.2003 (6), p.1197-1205
Ort / Verlag
Weinheim: WILEY-VCH Verlag
Erscheinungsjahr
2003
Link zum Volltext
Quelle
Wiley Online Library - AutoHoldings Journals
Beschreibungen/Notizen
The ligand α,α′‐bis{bis[1‐(1′‐methyl‐2′‐benzimidazolyl)methyl]amino}‐m‐xylene (L‐55) forms the complexes [CuI2(L‐55)(MeCN)2](PF6)2 (1) and [CuII2(L‐55)(OMe)2][ClO4]2 (2), in which an extremely weak axial amine interaction is imposed by the small five‐membered benzimidazole chelating ring units. This structural feature has been characterized by X‐ray crystal structure determination. In 1, the CuI centers are three‐coordinate with ligation from two benzimidazolyl and one acetonitrile N‐donors, in a slightly distorted trigonal arrangement. In 2, each CuII center has a distorted square‐planar geometry and coordinates to the benzimidazolyl N atoms and the bridging methoxy groups in the basal positions, with a much weaker interaction with the tertiary amine N in an apical position. These structural features affect the reactivities of the copper(I)− and copper(II)−L‐55 complexes toward dioxygen and hydrogen peroxide, respectively. [CuI2(L‐55)(MeCN)2]2+ does not produce a stable peroxo complex, but undergoes an irreversible oxidation to copper(II) species, while [CuII2(L‐55)(H2O)2]4+ reacts slowly with hydrogen peroxide to undergo regiospecific hydroxylation of the ligand at one benzylic carbon atom, which causes decomposition of the complex. [Cu2(L‐55)(H2O)2]4+ is easily converted into its bis(μ‐hydroxo) adduct [Cu2(L‐55)(OH)2]2+. This pH‐driven equilibrium was monitored by paramagnetic 1H NMR spectroscopy, and the solution magnetic properties of the complexes were determined by the Evans susceptibility method. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
Sprache
Englisch
Identifikatoren
ISSN: 1434-1948
eISSN: 1099-0682
DOI: 10.1002/ejic.200390155
Titel-ID: cdi_crossref_primary_10_1002_ejic_200390155
Format
–
Schlagworte
Bioinorganic chemistry
,
Copper
,
Dioxygen activation
,
Enzyme models
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