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次甲基硅SiH与HF反应的热力学及动力学性质研究
引用本文:司维江,居冠之.次甲基硅SiH与HF反应的热力学及动力学性质研究[J].无机化学学报,2002,18(8):782-786.
作者姓名:司维江  居冠之
作者单位:1. 山东理工大学化学工程学院,淄博,255091
2. 南京大学化学化工学院,配位化学国家重点实验室,介观材料科学实验室,南京,210093
基金项目:国家自然科学基金资助项目(No.20173027)
摘    要:在量子化学对SiH与HF反应计算的基础上,运用统计热力学和Wigner校正的Eyring过渡态理论计算了该反应在200~2000K温度范围内的热力学函数、平衡常数、频率因子A和速率常数随温度的变化。计算结果表明该反应在低温下具有热力学优势,而在高温下具有动力学优势。该反应在研究的温度范围内是一放热、熵减少的反应,反应的速率常数随温度的升高而增大,且服从Arrhenius定律。

关 键 词:次甲基硅插入反应  热力学及动力学性质

Thermodynamic and Kinetic Studies on the Reaction of Silylidyne Insertion Into HF
SI Wei-Jiang and JU Guan-Zhi.Thermodynamic and Kinetic Studies on the Reaction of Silylidyne Insertion Into HF[J].Chinese Journal of Inorganic Chemistry,2002,18(8):782-786.
Authors:SI Wei-Jiang and JU Guan-Zhi
Institution:College of Chemical Engineering, Shandong University of Technology, Zibo 255091 and School of Chemistry and Chemical Engineering, State Key Laboratory of Coordination Chemistry, Laboratory of Mesoscopic Material Science, Nanjing University, Nanjing 210093
Abstract:On the basis of quantum chemical study of the reaction of silylidyne insertion into HF, the statistical ther- modynamics and Eyring transition state theory with Wigner correction are used to estimate the thermodynamic functions, the equilibrium constants, A factors and the rate constants of this reaction in temperature range from 200 to 200OK. The results of calculation show that the reaction of SiH insertion into HF is thermodynamically dominant at low temperature and kinetically favored at high temperature. The statistical thermodynamic calculation shows that this reaction is exothermic and of entropy decrease at 200 ~ 2000K. The kinetic calculation results indicate that this reaction obeys the Arrhenius rate law, and the rate constant of this reaction increases with increasing temperature.
Keywords:silylidyne insertion reaction  thermodynamic and kinetic studies
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