In:
Angewandte Chemie International Edition, Wiley, Vol. 60, No. 42 ( 2021-10-11), p. 23018-23024
Abstract:
Cu I /TEMPO (TEMPO=2,2,6,6‐tetramethylpiperidinyloxyl) catalyst systems are versatile catalysts for aerobic alcohol oxidation reactions to selectively yield aldehydes. However, several aspects of the mechanism are yet unresolved, mainly because of the lack of identification of any reactive intermediates. Herein, we report the synthesis and characterization of a dinuclear [ L1 2 Cu 2 ] 2+ complex 1 , which in presence of TEMPO can couple the catalytic 4 H + /4 e − reduction of O 2 to water to the oxidation of benzylic and aliphatic alcohols. The mechanisms of the O 2 ‐reduction and alcohol oxidation reactions have been clarified by the spectroscopic detection of the reactive intermediates in the gas and condensed phases, as well as by kinetic studies on each step in the catalytic cycles. Bis(μ‐oxo)dicopper(III) ( 2 ) and bis(μ‐hydroxo)dicopper(II) species 3 are shown as viable reactants in oxidation catalysis. The present study provides deep mechanistic insight into the aerobic oxidation of alcohols that should serve as a valuable foundation for ongoing efforts dedicated towards the understanding of transition‐metal catalysts involving redox‐active organic cocatalysts.
Type of Medium:
Online Resource
ISSN:
1433-7851
,
1521-3773
DOI:
10.1002/anie.202108442
Language:
English
Publisher:
Wiley
Publication Date:
2021
detail.hit.zdb_id:
2011836-3
detail.hit.zdb_id:
123227-7