Cover Feature: On the Metal Cooperativity in a Dinuclear Copper–Guanidine Complex for Aliphatic C−H Bond Cleavage by Dioxygen (Chem. Eur. J. 48/2019)
Metal cooperativity in a binuclear copper–guanidine complex enables aliphatic hydroxylation as known from the enzyme α‐hydroxylating monooxygenase (PHM). In the model complex reported, one copper atom is responsible for dioxygen activation, whereas the role of the second copper atom is to stabilize...
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Published in | Chemistry : a European journal Vol. 25; no. 48; p. 11173 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
27.08.2019
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Subjects | |
Online Access | Get full text |
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Summary: | Metal cooperativity in a binuclear copper–guanidine complex enables aliphatic hydroxylation as known from the enzyme α‐hydroxylating monooxygenase (PHM). In the model complex reported, one copper atom is responsible for dioxygen activation, whereas the role of the second copper atom is to stabilize the product after C−H bond cleavage. Related mononuclear copper complexes, which do not profit from this cooperative effect, display no hydroxylation activity. More information can be found in the Full Paper by H.‐J. Himmel et al. on page 11257. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201902620 |