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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Double N-H bond activation of N,N′-bis-substituted hydrazines with stable N-heterocyclic silylene
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Double N-H bond activation of N,N′-bis-substituted hydrazines with stable N-heterocyclic silylene

机译:N,N'-双取代肼与稳定的N-杂环亚甲硅烷基的双N-H键活化

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摘要

The reaction of N-heterocyclic silylene (NHSi) L [L = CH{(CCH _2)(CMe)(2,6-iPr _2C _6H _3N) _2}Si] with benzoylhydrazine, 1,2-dicarbethoxyhydrazine, 1,2-diacetylhydrazine and 1,2-bis(tert-butoxycarbonyl)hydrazine in 1:1 molar ratio resulted in compounds 1-4 with an almost quantitative yield and five coordinate silicon atoms. Compounds 1-4 were formed by double N-H bond activation by deliberate selection of N,N′-bis-substituted hydrazine compounds bearing the -C(O)NHNH- unit. Compounds 1-4 were characterized by NMR spectroscopy, EI-MS and elemental analysis. The molecular structures of compounds 1-3 were unambiguously established by single crystal X-ray structural analysis.
机译:N-杂环甲硅烷基(NHSi)L [L = CH {(CCH _2)(CMe)(2,6-iPr _2C _6H _3N)_2} Si]与苯甲酰肼,1,2-二碳乙氧基肼,1,2-摩尔比为1:1的二乙酰肼和1,2-双(叔丁氧羰基)肼生成的化合物1-4的收率基本定量,并带有五个配位硅原子。化合物1-4是通过有选择地选择带有-C(O)NHNH-单元的N,N'-双取代肼化合物通过双N-H键活化而形成的。通过NMR光谱,EI-MS和元素分析表征化合物1-4。通过单晶X射线结构分析清楚地确定了化合物1-3的分子结构。

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