Synthesis and isolation of the stable diaryldibromodisilene, Bbt(Br)SiSi(Br)Bbt, has been accomplished for the first time. The dibromodisilene underwent substitution reactions with organometallic reagents on the low-coordinated silicon atom to afford the corresponding substituted disilenes. Furthermore, the reaction of 1 with t-BuLi afforded the corresponding 1,2-diaryldisilyne, BbtSi[triple bond]SiBbt, the characters of which were revealed by spectroscopic and crystallographic analyses.
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http://dx.doi.org/10.1021/ja8061002 | DOI Listing |
J Am Chem Soc
September 2024
Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Osaka 577-8502, Japan.
Chemistry
October 2023
Department of Nanoscience, Joint School of Nanoscience and Nanoengineering, University of North Carolina at Greensboro, Greensboro, NC 27401, USA.
There have been remarkable advances in the syntheses and applications of groups 13 and 14 homonuclear ethene analogues. However, successes are largely limited to aryl- and/or silyl-substituted species. Analogues bearing two or more heteroatoms are still scarce.
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February 2022
Westfälische-Willhelms-Universität Münster, Institut für Anorganische und Analytische Chemie, Corrensstraße 28-30, 48149 Münster, Germany.
The reductive debromination of {N(SiMe)Ph}SiBr1 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 NHC and DMAP, respectively.
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March 2021
Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aramakiazaaoba, Aoba-ku, Sendai 980-8578, Japan.
π-Electron systems of silicon have attracted attention because of their narrow HOMO-LUMO gap and high reactivity, but the structural diversity remains limited. Herein, new dialkylboryl-substituted disilenes were synthesized by the selective desilylation-borylation of the corresponding trimethylsilyl-substituted disilenes. The dialkylboryl-substituted disilenes were fully characterized by a combination of NMR spectroscopy, MS spectrometry, single-crystal X-ray diffraction analysis, and theoretical calculations.
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October 2020
Krupp-Chair of General and Inorganic Chemistry, Saarland University, 66123 Saarbrücken, Germany.
Recent studies of low-valent main group species underscore their resemblance to transition metal complexes with regards to the ability to activate small molecules. Here, we report synthesis and full characterisation of the persistent (hypersilyl)(pentamethylcyclopentadienyl)silylene Cp*[(Me3Si)3Si]Si: as well as its unique reactivity. Silylene Cp*[(Me3Si)3Si]Si: activates dihydrogen to give the corresponding dihydrosilane Cp*[(Me3Si)3Si]SiH2 at particularly mild conditions as well as ethylene to afford the three-membered cyclic silirane c-Cp*[(Me3Si)3Si]Si(H2CCH2).
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