Issue 10, 2015

Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies

Abstract

Diboron (B2pin2) has been identified as an efficient and environmentally benign reducing reagent for reductive coupling reactions for the first time, which enables the nickel-catalyzed reductive tetramerization of alkynes to be performed with high efficiency. Mechanistic and kinetic studies indicate that the facile reductive elimination to form the B–B bond from the dinuclear Ni–Ni complexes is responsible for the high efficiency. The activation enthalpy (ΔH = 56.5 kJ mol−1), entropy (ΔS = −128 J mol−1 K−1) and the substituent effect (ρ = 1.43) on this reaction were obtained.

Graphical abstract: Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2014
Accepted
10 Dec 2014
First published
11 Dec 2014

Chem. Commun., 2015,51, 1850-1853

Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies

G. Zhang, Y. Xie, Z. Wang, Y. Liu and H. Huang, Chem. Commun., 2015, 51, 1850 DOI: 10.1039/C4CC08703H

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