4.5 Article

Reaction of disilagermirenes with phenylacetylene: from a germasilene -Ge=Si- to a metalladiene of the type -Si=Ge-C=C-

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JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 636, 期 1-2, 页码 41-48

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ELSEVIER SCIENCE SA
DOI: 10.1016/S0022-328X(01)00807-5

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conjugation; cycloaddition; germasilene; metalladiene; phenylacetylene; silole

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The reaction of tetrakis[di-tert-butyl(methyl)silyl]-2-disilagermirene (1b) with phenylacetylene at room temperature produced highly air- and moisture-sensitive bright orange crystals of 1, 1,2,3-tetrakis[di-tert-butyl(methyl)silyl]-4-phenyl-1,2-disila-3-germacyclopenta-2,4-diene (2b), which represents a previously unknown metalladiene with one Si=Ge and one C=C double bond. The crystal structure of 2b was determined by X-ray crystallography, which showed a trans-bent configuration around the Si=Ge double bond with a bond length of 2.250(1) Angstrom. The reaction mechanism to form 2b, the question of conjugation of the two double bonds in a cyclopentadiene ring of 2b, as well as its reactivity are discussed. The reaction of tetrakis[di-tert-butyl(methyl)silyl]-1-disilagermirene (1a), which is an isomer of 1b, with phenylacetylene is also examined. (C) 2001 Elsevier Science B.V. All rights reserved.

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