首页 | 本学科首页   官方微博 | 高级检索  
     检索      

丁酸甲酯单分子解离的非谐振效应
引用本文:丁杨,宋立国,余忆玄,姚丽,林圣贤.丁酸甲酯单分子解离的非谐振效应[J].物理化学学报,2016,32(11):2685-2692.
作者姓名:丁杨  宋立国  余忆玄  姚丽  林圣贤
作者单位:1 大连海事大学轮机工程学院,辽宁大连1160262 台湾交通大学应用化学系,台湾新竹10764
基金项目:the Major Research Plan of the National Natural Science Foundation of China(91441132);Fundamental Research Funds for the Central Universities, China(3132016127);Fundamental Research Funds for the Central Universities, China(3132016326)
摘    要:使用MP2/6-311++G(2d,2p)方法和基组,计算了丁酸甲酯单分子解离反应体系详细的势能面。应用RRKM理论,计算了在1000-5000 K的温度范围内的正则系综的速率常数。与此同时,在微正则系综下,我们计算了温度为1000-5000 K对应的能量从451.92到1519.52 kJ·mol-1的速率常数。计算结果表明反应通道2、4和5的非谐振效应比较明显。因此对于丁酸甲酯单分子解离反应体系来说其非谐振效应是不能忽视的。

关 键 词:非谐振效应  单分子解离反应  RRKM理论  速率常数  
收稿时间:2016-03-16

Anharmonic Effect of the Decomposition Reaction of Methyl Butanoate
Yang DING,Li-Guo SONG,Yi-Xuan YU,Li YAO,Sheng-Hsien LIN.Anharmonic Effect of the Decomposition Reaction of Methyl Butanoate[J].Acta Physico-Chimica Sinica,2016,32(11):2685-2692.
Authors:Yang DING  Li-Guo SONG  Yi-Xuan YU  Li YAO  Sheng-Hsien LIN
Institution:1. Marine Engineering College, Dalian Maritime University, Dalian 116026, P. R. China;2. Department of Applied Chemistry, National Chiao-Tung University, Hsin-chu 10764, Taiwan, P. R. China
Abstract:In this paper, we have used the MP2/6-311++G(2d, 2p) method to conduct a detailed investigation of the potential energy surface for the unimolecular dissociation reaction of methyl butanoate (MB). We have also used the Rice-Ramsperger-Kassel-Marcus (RRKM) theory to calculate the rate constants of the canonical and microcanonical systems at temperatures and total energies ranging from 1000 to 5000 K and 451.92 to 1519.52 kJ·mol-1, respectively. The results indicated that there was an obvious anharmonic effect for the TS2, TS4 and TS5 pathways, and that this effect was too pronounced to be neglected for the unimolecular dissociation reactions of MB.
Keywords:Anharmonic effect  Unimolecular decomposition reaction  RRKM theory  Rate constant  
点击此处可从《物理化学学报》浏览原始摘要信息
点击此处可从《物理化学学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号