Issue 14, 2022

Metalation-induced denitrogenative reductive coupling of isocyanides on a silylene-bridged nickel cluster

Abstract

The denitrogenative reductive coupling of two molecules of CNtBu to afford a disilylketenimine with an aza-disilacyclobutane skeleton was achieved on a multinuclear silylene-bridged Ni cluster framework in the absence of any strong reducing reagents. During this reaction, sequential cleavage of a C[triple bond, length as m-dash]N bond and formation of a C[triple bond, length as m-dash]C bond involving two molecules of CNtBu were achieved on a nickel cluster surrounded by four silylene moieties. First, the cleavage of the C[triple bond, length as m-dash]N bond of one molecule of CNtBu provided a silylene-supported carbide and an NtBu moiety on the dinuclear nickel skeleton. Further metalation induced coupling between the carbide moiety and an additional molecule of CNtBu on the pentanuclear nickel-cluster framework to form a Image ID:d1sc06935g-t1.gif moiety via formation of a C[triple bond, length as m-dash]C bond. Thermolysis of this pentanuclear cluster produced a disilylketenimine with an aza-disilacyclobutane skeleton in 58% yield.

Graphical abstract: Metalation-induced denitrogenative reductive coupling of isocyanides on a silylene-bridged nickel cluster

Supplementary files

Article information

Article type
Edge Article
Submitted
11 Dec 2021
Accepted
11 Mar 2022
First published
15 Mar 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2022,13, 4115-4121

Metalation-induced denitrogenative reductive coupling of isocyanides on a silylene-bridged nickel cluster

K. Shimamoto and Y. Sunada, Chem. Sci., 2022, 13, 4115 DOI: 10.1039/D1SC06935G

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