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A search for thermal isomerization of olefins to carbenes. Thermal generations of the silicon-nitrogen double bond

机译:寻找将烯烃热异构化为卡宾。硅氮双键的热生成

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摘要

Thermal isomerization of an olefin to a carbene is observed only in a few strained olefins. Attempts to observe a 1,2-silyl migration to form a carbene from a simple olefin were not successful. The olefins studied are stable at lower temperature and decomposed to smaller molecules at higher temperature probably via a radical process. The gas-phase thermal behavior of a series of organic and organosilicon compounds was studied by stirred-flow reactor (SFR) pyrolysis. Kinetic parameters were determined in the gas phase for various hydrocarbons and organosilicon compounds. The activation energies and log As of the compounds studied are in the normal range of olefinic cis-trans isomerization proceeding by a singlet biradical mechanism;The substituent effect on the thermal isomerization of olefins was discussed. The substitution of phenyl, t-butyl, and trimethylsilyl groups on the double bond lowers the olefinic cis-trans isomerization Oil, Gas, and Energy;A new reaction, gas-phase thermal isomerization of a silacyclobutene to silylallene, was discovered. The mechanism of the isomerization was studied by deuterium-labeling experiments;Intermediates containing silicon-nitrogen double bonds were generated in the gas phase by [beta]-elimination of trimethylmethoxysilane and retroene elimination of propene. The 1,2-silyl migration of silanimine to aminosilylene was observed. This is the first observation of a silanimine-to-aminosilylene isomerization. The aminosilylene formed was trapped by 1,3-butadiene and the structure of the trapping product was proven by comparison of its spectroscopic data with that of an authentic sample synthesized by an independent route. The isomerization of silanimine to aminosilylene by 2,3-allyl migration was not observed. Dimers of silanimine are formed in the absence of trapping reagents;Different approaches to silicon-nitrogen double bond were also explored. Attempts to obtain evidence for silapyridine, an unknown compound, both theoretically and experimentally, were not successful.
机译:仅在少数应变烯烃中观察到烯烃热异构化为卡宾。尝试观察到1,2-甲硅烷基迁移以从简单烯烃形成卡宾的尝试并不成功。所研究的烯烃在较低温度下稳定,并可能通过自由基过程在较高温度下分解为较小的分子。通过搅拌流反应器(SFR)热解研究了一系列有机和有机硅化合物的气相热行为。在气相中确定了各种烃和有机硅化合物的动力学参数。所研究化合物的活化能和log As均在单链双自由基机理下进行的顺式-顺式异构化的正常范围内;讨论了取代基对烯烃热异构化的影响。双键上的苯基,叔丁基和三甲基甲硅烷基的取代降低了烯烃的顺式-反式异构化的油,气和能量;发现了一种新的反应,即硅环丁烯气相热异构化为甲硅烷基丙二烯。通过氘标记实验研究了异构化的机理;通过β-消除三甲基甲氧基硅烷和丙烯的复古烯消除,在气相中产生了含有硅-氮双键的中间体。观察到甲硅烷基胺向氨基甲硅烷基的1,2-甲硅烷基迁移。这是甲硅烷基胺向氨基甲硅烷基异构化的首次观察。形成的氨基亚甲硅烷基被1,3-丁二烯捕获,并且通过将其光谱数据与通过独立途径合成的真实样品的光谱数据进行比较,证明了捕获产物的结构。没有观察到通过2,3-烯丙基迁移将硅苯胺转化为氨基亚甲硅烷基。在没有捕集剂的情况下会形成硅烷胺的二聚体;还探索了不同的硅氮双键方法。尝试从理论上和实验上获得关于未知化合物西拉吡啶的证据均未成功。

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  • 作者

    Zhang, Xianping;

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  • 年度 1990
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  • 原文格式 PDF
  • 正文语种 en
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