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Syntheses and crystal structure determination of hexacoordinated silicon-complexes with dimethylpyridines [German]

机译:含二甲基吡啶的六配位硅配合物的合成和晶体结构测定[德国]

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摘要

Trichlorosilane, HSiCl3, forms with 3,4-dimethylpyridine in aprotic solvents a crystalline 1:2-compound which is stable at room temperature and readily soluble in CHCl3. Colourless crystals of the dicationic complex, [H2Si(3,4-dimethylpyridine)(4)](2+)2Cl(-) . 6 CHCl3 (verified by X-ray structure analysis) are obtained by dismutation of HSiCl3(3,4-dimethylpyridine)(2) in CHCl3 within one week at room temperature. Si-29 NMR indicates that SiCl4 is generated as a second product. H2SiCl2 with 2,4-dimethylpyridine as well as MeHSiBr2 with 3,5-dimethylpyridine in aprotic solvents form 1:2-compounds stable at room temperature. X-ray structure analyses in both cases establish neutral-complexes with a hexa-coordinated silicon atom. [References: 21]
机译:三氯硅烷HSiCl3与3,4-二甲基吡啶在非质子传递溶剂中形成结晶的1:2化合物,该化合物在室温下稳定并易溶于CHCl3。双金属配合物[H2Si(3,4-二甲基吡啶)(4)](2+)2Cl(-)的无色晶体。通过在室温下一周内将HSiCl3(3,4-二甲基吡啶)(2)在CHCl3中进行歧化得到6 CHCl3(通过X射线结构分析验证)。 Si-29 NMR表明产生了SiCl4作为第二产物。在质子惰性溶剂中,带有2,4-二甲基吡啶的H2SiCl2和带有3,5-二甲基吡啶的MeHSiBr2形成在室温下稳定的1:2化合物。两种情况下的X射线结构分析均建立了具有六配位硅原子的中性络合物。 [参考:21]

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