{"title":"单分子反应动力学中的模式特异性问题","authors":"W. Miller","doi":"10.1155/LC.2.243","DOIUrl":null,"url":null,"abstract":"Unimolecular decomposition following state-specific laser excitation is considered. If \nthe transition state for the unimolecular reaction possesses any geometrical symmetry, \nthen it is shown that this can lead to mode-specificity in the decay rates (i.e., different \nstates with essentially the same total energy and angular momentum react at significantly \ndifferent rates). This is illustrated for a model problem of two coupled oscillators (the \nHenon–Heiles potential) and also for the unimolecular dissociation of formaldehyde, \nH2CO→H2","PeriodicalId":296295,"journal":{"name":"Laser Chemistry","volume":"10 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Question of mode-specificity in unimolecular reaction dynamics\",\"authors\":\"W. Miller\",\"doi\":\"10.1155/LC.2.243\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Unimolecular decomposition following state-specific laser excitation is considered. If \\nthe transition state for the unimolecular reaction possesses any geometrical symmetry, \\nthen it is shown that this can lead to mode-specificity in the decay rates (i.e., different \\nstates with essentially the same total energy and angular momentum react at significantly \\ndifferent rates). This is illustrated for a model problem of two coupled oscillators (the \\nHenon–Heiles potential) and also for the unimolecular dissociation of formaldehyde, \\nH2CO→H2\",\"PeriodicalId\":296295,\"journal\":{\"name\":\"Laser Chemistry\",\"volume\":\"10 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laser Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/LC.2.243\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laser Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/LC.2.243","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Question of mode-specificity in unimolecular reaction dynamics
Unimolecular decomposition following state-specific laser excitation is considered. If
the transition state for the unimolecular reaction possesses any geometrical symmetry,
then it is shown that this can lead to mode-specificity in the decay rates (i.e., different
states with essentially the same total energy and angular momentum react at significantly
different rates). This is illustrated for a model problem of two coupled oscillators (the
Henon–Heiles potential) and also for the unimolecular dissociation of formaldehyde,
H2CO→H2