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Tuning Inner-Sphere Electron Transfer in a Series of Copper/Nitrosoarene Adducts.

Author(s): Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X

Inorg Chem. 2020 Feb 19;: Authors: Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X

Article GUID: 32073833

A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols.

Author(s): Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP

Chem Sci. 2016 Jan 01;7(1):358-369 Authors: Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP

Article GUID: 29861988

Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.

Author(s): Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A

J Org Chem. 2016 07 01;81(13):5401-16 Authors: Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A

Article GUID: 27231755

Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate.

Author(s): Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X

Dalton Trans. 2016 Jul 05;45(27):11109-19 Authors: Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X

Article GUID: 27328176


Title:Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate.
Authors:Chaloner LKhomutovskaya AThomas FOttenwaelder X
Link:https://www.ncbi.nlm.nih.gov/pubmed/27328176?dopt=Abstract
Category:Dalton Trans
PMID:27328176
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montreal, H4B 1R6, Canada. dr.x@concordia.ca.
2 Équipe de Chimie Inorganique Redox, Département de Chimie Moléculaire, Université Joseph Fourier, 38041 Grenoble, Cedex 9, France.

Description:

Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate.

Dalton Trans. 2016 Jul 05;45(27):11109-19

Authors: Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X

Abstract

We report a detailed investigation of the formation and self-decomposition of Cu(ii)-hydroperoxo intermediates under the influence of second-coordination-sphere features provided by a cryptand. In solution, an equilibrium between two copper complexes with square-planar and square-pyramidal geometries was identified. Upon addition of H2O2/Et3N, two copper(ii)-hydroperoxo intermediates formed at different rates. Their decomposition via self-oxidation was probed by deuterating select positions on the cryptand. This led to a small kinetic isotope effect of 1.5. Mass spectrometry analysis of the demetallated organic products is consistent with a direct oxygen-atom transfer to a tertiary amine on the cryptand, forming an N-oxide, unlike other models of copper mononuclear monooxygenase enzymes.

PMID: 27328176 [PubMed - indexed for MEDLINE]