二茂铁基n -杂环锡炔[Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn]的合成、结构和反应性

N. Weyer, C. Bruhn, U. Siemeling
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引用次数: 0

摘要

摘要以SnCl2和锂酰胺[Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Li2]为原料合成了n -杂环锡炔[Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn](1)。化合物1在环境条件下对H2、CO、CO2和MeI都是惰性的。用H2O和NH3分别观察到立即水解和氨解。虽然1与硫原(O2, S8, Se8)的氧化反应只能得到难处理的物质,但与Ph2Se2的氧化反应得到了[Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn(SePh)2](2)。化合物1和2已通过单晶x射线衍射进行了结构表征。化合物2表现出与弱氢键相容的分子内CH⋯Se接触。
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Synthesis, structure, and reactivity of the ferrocene-based N-heterocyclic stannylene [Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn]
Abstract The N-heterocyclic stannylene [Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn] (1) has been synthesised from SnCl2 and the lithium amide [Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Li2]. Compound 1 is inert towards H2, CO, CO2, and MeI under ambient conditions. Immediate hydrolysis and ammonolysis was observed with H2O and NH3, respectively. While oxidation reactions of 1 with chalcogens (O2, S8, Se8) afforded only intractable material, the reaction with Ph2Se2 cleanly furnished [Fe{(η5-C5H4)NC6H3-2,6-iPr2}2Sn(SePh)2] (2). Compounds 1 and 2 have been structurally characterised by single-crystal X-ray diffraction. Compound 2 exhibits an intramolecular CH⋯Se contact compatible with a weak hydrogen bond.
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