Molecular CuII-O-CuII Complexes: Still Waters Run Deep

被引:81
|
作者
Haack, Peter [1 ]
Limberg, Christian [1 ]
机构
[1] Humboldt Univ, Inst Chem, D-12489 Berlin, Germany
关键词
biomimetic reactions; copper; dinuclear complexes; oxidation; oxo compounds; PARTICULATE METHANE MONOOXYGENASE; TETRANUCLEAR COPPER(II) COMPLEX; CRYSTAL-STRUCTURE; STRUCTURAL-CHARACTERIZATION; ACTIVE-SITE; PHYSICAL-PROPERTIES; DICOPPER COMPLEXES; SPECTROSCOPIC PROPERTIES; DIOXYGEN REACTIVITY; ARENE HYDROXYLATION;
D O I
10.1002/anie.201309505
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on O-2 activation at ligated Cu-I is fueled by its biological relevance and the quest for efficient oxidation catalysts. A rarely observed reaction is the formation of a Cu-II-O-Cu-II species, which is more special than it appears at first sight: a single oxo ligand between two Cu-II centers experiences considerable electron density, and this makes the corresponding complexes reactive and difficult to access. Hence, only a small number of these compounds have been synthesized and characterized unequivocally to date, and as biological relevance was not apparent, they remained unappreciated. However, recently they moved into the spotlight, when Cu-II-O-Cu-II cores were proposed as the active species in the challenging oxidation of methane to methanol at the surface of a Cu-grafted zeolite and in the active center of the copper enzyme particulate methane monooxygenase. This Minireview provides an overview of these systems with a special focus on their reactivity and spectroscopic features.
引用
收藏
页码:4282 / 4293
页数:12
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