Issue 8, 2022

A strongly twisted Si[double bond, length as m-dash]Si bond with resemblance to a buckled dimer in an unexpected isomer of hexasilabenzene

Abstract

The reductive debromination of {N(SiMe3)Ph}SiBr31 with Rieke magnesium yields the six-vertex amido-substituted silicon cluster 2 with zwitterionic character that represents an unprecedented isomer of hexasilabenzene. The topology of Si1 and Si2 in 2 has bonding features of a highly twisted disilene and resembles that of a buckled dimer of Si(100)2 × 1 reconstructed surfaces. Cluster 2 forms the adducts 3 and 4 with NHCMe4 and DMAP, respectively. The NHC adduct 4 additionally coordinates to BH3 which affords the saturated cluster BH3NHCMe4Si6{N(SiMe3)Ph}6 (5). Furthermore, 2 undergoes addition with MeI and iodine to form the halogenated silicon clusters 6 and 7, respectively.

Graphical abstract: A strongly twisted Si [[double bond, length as m-dash]] Si bond with resemblance to a buckled dimer in an unexpected isomer of hexasilabenzene

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2022
Accepted
28 Jan 2022
First published
01 Feb 2022

Dalton Trans., 2022,51, 3254-3262

A strongly twisted Si[double bond, length as m-dash]Si bond with resemblance to a buckled dimer in an unexpected isomer of hexasilabenzene

J. Helmer, A. Hepp and F. Lips, Dalton Trans., 2022, 51, 3254 DOI: 10.1039/D2DT00259K

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