Dimetallic Dioxygen Activation Leading to a Doubly Oxygen-Bridged Dirhodium Complex
Ready cleavage of dioxygen and its selective insertion into Rh–alkene bonds occurs in the presence of [{Rh(PhN3Ph)(C8H12)}n] (n=1 and 2). The structure of the resulting dirhodadioxetane complex (see picture) and kinetic measurements support a dimetallic mechanism for this process that occurs with 10...
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Veröffentlicht in: | Angewandte Chemie International Edition 2005-05, Vol.44 (21), p.3267-3271 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Ready cleavage of dioxygen and its selective insertion into Rh–alkene bonds occurs in the presence of [{Rh(PhN3Ph)(C8H12)}n] (n=1 and 2). The structure of the resulting dirhodadioxetane complex (see picture) and kinetic measurements support a dimetallic mechanism for this process that occurs with 100 % atom economy. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.200463073 |