Chemistry Letters · 1987 · 79 citations · 8 references
Materials ScienceInorganic ChemistryOrganic Material ChemistrySi=si BondEngineeringAir-stable DisileneBulky SubstituentsOrganic ChemistryOrganometallic PolymerChemistryAir-stable TetrakisSynthetic ChemistryInorganic Synthesis
Abstract The most air-stable disilene, tetrakis(2,4,6-triisopropylphenyl) disilene was obtained by the direct treatment of dichloromonosilane, bis(2,4,6-triisopropylphenyl)dichlorosilane, with lithium naphthalenide. The Si=Si bond, the distance being 2.144 Å via X-ray structure analysis, was found to be sterically covered with the four bulky substituents.
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X-ray crystal structures for two disilenes
Mark J. Fink, Michael J. Michalczyk, Kenneth J. Haller et al. · Organometallics · 1984 · 149 citations
Molecular structure of tetrakis(2,6-diethylphenyl)disilene
Satoru Masamune, Shu Murakami, James T. Snow et al. · Organometallics · 1984 · 75 citations