Issue 45, 2024

Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene

Abstract

The salt metathesis of a boryl-ethynyl lithium salt {[(HCDipN)2]B-CC-Li} with a monochlorosilylene [LSi(:)Cl; L = PhC(NtBu)2] produced an isolable boryl-ethynyl silylene {1; [(HCDipN)2]B–C[triple bond, length as m-dash]C–Si(L)}. The Si(II) center in 1 possesses a nonbonding lone pair and forms a covalent bond with the ethynyl group. The characterization of 1 was carried out by multinuclear NMR spectroscopy, single-crystal X-ray structure analysis and DFT calculations. Additionally, a reactivity study of 1 was conducted towards oxygen-containing and aryl C–F substrates.

Graphical abstract: Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene

Supplementary files

Article information

Article type
Communication
Submitted
28 Feb 2024
Accepted
07 May 2024
First published
08 May 2024

Chem. Commun., 2024,60, 5828-5831

Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene

W. Chen, H. Hu, J. Feng, L. Zhu and D. Wu, Chem. Commun., 2024, 60, 5828 DOI: 10.1039/D4CC00922C

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