Issue 24, 2016

Reduction of a diamidocarbene-supported borenium cation: isolation of a neutral boryl-substituted radical and a carbene-stabilized aminoborylene

Abstract

We have synthesized the first diamidocarbene (DAC)-supported borenium salt, [3][OTf], which was found to readily undergo two sequential 1-electron reductions. The first reduction forms a thermally robust, crystalline boryl-substituted DAC-centred radical () which has been fully characterized by XRD, EPR spectroscopy, and DFT analyses. The 1-electron reduction of resulted in the formation of a DAC-supported aminoborylene, 4, which has been characterized computationally and by multinuclear NMR spectroscopy.

Graphical abstract: Reduction of a diamidocarbene-supported borenium cation: isolation of a neutral boryl-substituted radical and a carbene-stabilized aminoborylene

Supplementary files

Article information

Article type
Paper
Submitted
21 Janv. 2016
Accepted
01 Febr. 2016
First published
01 Febr. 2016

Dalton Trans., 2016,45, 9820-9826

Reduction of a diamidocarbene-supported borenium cation: isolation of a neutral boryl-substituted radical and a carbene-stabilized aminoborylene

A. D. Ledet and T. W. Hudnall, Dalton Trans., 2016, 45, 9820 DOI: 10.1039/C6DT00300A

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