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ENERGIES OF ISOMERIZATION IN NITROMETHYL DERIVATIVES OF TERAZOL

机译:Terazol硝基甲基衍生物中异构化的能量

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摘要

Energies of combustion are measured and enthalpies of formation in the standard condition derivatives of 1,5 and 2,5 isomers of tetrazol (1-methyl-5-nitromethyltetrazol and 2-methyl-5-nitromethyltetrazol, 1-nitromethyl-5-methyltetrazol and 2-nitromethyl-5-methyltetrazol) are received. On the basis of the data received and available in the literature the thermochemical analysis of influence of the chemical nature and a place of connection of functional groups on values energy of isomerization in isomers of tetrazol is carried out. Energies of isomerization are estimated as the differences in enthalpies of formation of the same name derivatives of 1,5 and 2,5 isomers of tetrazol. It is established, that depending on a chemical nature and place of connection of functional groups the values of energy isomerization lays in limits from -29 up to + 35 kJ·mol~(-1).
机译:测量燃烧的能量,并在四唑(1-甲基-5-硝基甲基四唑和2-甲基-5-硝基甲基四唑,1-硝基甲基-5-甲基四唑和1-硝基甲基-5-甲基四唑和中)的标准条件衍生物中测量和形成的焓。收到2-硝基甲基-5-甲基四甲基四甲基四甲基四甲基四甲基四甲基四甲基四甲基四甲基苯并唑。在文献中收到的数据和可用的数据的基础上,进行了化学性质的影响和官能团的连接的能量的热化学分析,对四唑异构化的异构化值的能量。异构化的能量估计是形成硫唑的1,5和2,5异构体的相同名称衍生物的形成焓的差异。建立,取决于官能团的化学性质和官能团连接地点,能量异构化的值从-29到+ 35kJ·mol〜(-1)限制。

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