Issue 99, 2022

Markovnikov-selective double hydrosilylation of challenging terminal aryl alkynes under cobalt and iron catalysis

Abstract

Geminal bis(silanes) are unique compounds with interesting properties. The most straightforward way to access them is double hydrosilylation of alkynes, which was established only recently. Previous articles about transition metal-catalysed double hydrosilylation show that terminal aryl alkynes are a challenge. We report on cobalt(II) and iron(III) complexes with the easy-to-synthesise N,N,N-tridentate hydrazone ligand being active precatalysts in Markovnikov-selective double hydrosilylation of terminal aryl alkynes. The influence of the hydrazone ligand structure and the potential role of the sodium triethylborohydride activator were studied. Sets of geminal bis(silanes) with two identical or different silyl groups were synthesised, showing the applicability of the reported method.

Graphical abstract: Markovnikov-selective double hydrosilylation of challenging terminal aryl alkynes under cobalt and iron catalysis

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2022
Accepted
12 Oct 2022
First published
24 Nov 2022
This article is Open Access
Creative Commons BY license

Chem. Commun., 2022,58, 13763-13766

Markovnikov-selective double hydrosilylation of challenging terminal aryl alkynes under cobalt and iron catalysis

Ł. Banach, D. Brykczyńska, A. Gorczyński, B. Wyrzykiewicz, M. Skrodzki and P. Pawluć, Chem. Commun., 2022, 58, 13763 DOI: 10.1039/D2CC04015H

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