Issue 17, 2019

Synthesis of a hydrogen-bridged tetraborane(6): a substituent effect of a diaminoboryl group toward the B–B multiple bond character

Abstract

A hydrogen-bridging tetraborane(6) was synthesized from boryllithium, a boron nucleophile, in three steps. The structural and spectroscopic analyses of the tetraborane(6) revealed σ-donor and π-acceptor effects of diaminoboryl substituents toward the central B–B moiety having a multiple bond character. DFT calculations also supported the experimentally observed substituent effect of the boryl group.

Graphical abstract: Synthesis of a hydrogen-bridged tetraborane(6): a substituent effect of a diaminoboryl group toward the B–B multiple bond character

Supplementary files

Article information

Article type
Communication
Submitted
14 Meur. 2019
Accepted
18 Meur. 2019
First published
20 Meur. 2019

Dalton Trans., 2019,48, 5496-5499

Synthesis of a hydrogen-bridged tetraborane(6): a substituent effect of a diaminoboryl group toward the B–B multiple bond character

A. Yagi, H. Kisu and M. Yamashita, Dalton Trans., 2019, 48, 5496 DOI: 10.1039/C9DT01117J

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