Volume 129, Issue 40 pp. 12436-12440
Zuschrift

Group 6 Transition-Metal/Boron Frustrated Lewis Pair Templates Activate N2 and Allow its Facile Borylation and Silylation

Dr. Antoine Simonneau

Corresponding Author

Dr. Antoine Simonneau

CNRS, LCC (Laboratoire de Chimie de Coordination), 205, route de Narbonne, BP44099, 31077 Toulouse Cedex 4, France

Université de Toulouse, UPS, INPT; LCC, 31077 Toulouse Cedex 4, France

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Raphaël Turrel

Raphaël Turrel

CNRS, LCC (Laboratoire de Chimie de Coordination), 205, route de Narbonne, BP44099, 31077 Toulouse Cedex 4, France

Université de Toulouse, UPS, INPT; LCC, 31077 Toulouse Cedex 4, France

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Dr. Laure Vendier

Dr. Laure Vendier

CNRS, LCC (Laboratoire de Chimie de Coordination), 205, route de Narbonne, BP44099, 31077 Toulouse Cedex 4, France

Université de Toulouse, UPS, INPT; LCC, 31077 Toulouse Cedex 4, France

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Prof. Dr. Michel Etienne

Prof. Dr. Michel Etienne

CNRS, LCC (Laboratoire de Chimie de Coordination), 205, route de Narbonne, BP44099, 31077 Toulouse Cedex 4, France

Université de Toulouse, UPS, INPT; LCC, 31077 Toulouse Cedex 4, France

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First published: 02 August 2017
Citations: 42

Abstract

The reaction of trans-[M(N2)2(dppe)2] (M=Mo, 1Mo, M=W, 1W) with B(C6F5)3 (2) provides the adducts [(dppe)2M=N=N-B(C6F5)3] (3) which can be regarded as M/B transition-metal frustrated Lewis pair (TMFLP) templates activating dinitrogen. Easy borylation and silylation of the activated dinitrogen ligands in complexes 3 with a hydroborane and hydrosilane occur by splitting of the B−H and Si−H bonds between the N2 moiety and the perfluoroaryl borane. This reactivity of 3 is reminiscent of conventional frustrated Lewis pair chemistry and constitutes an unprecedented approach for the functionalization of dinitrogen.

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