OH Roaming as a Key Pathway in the Anti-CH3CHOO + H2O Reaction Yielding CH3COOH and H2O

被引:0
作者
Liu, Lijie [1 ,2 ]
Wu, Hao [2 ]
Fu, Yanlin [2 ]
Lu, Xiaoxiao [2 ,5 ]
Wang, Xingan [1 ,3 ]
Zhang, Dong H. [2 ,3 ,4 ]
Fu, Bina [2 ,3 ,4 ]
机构
[1] Univ Sci & Technol China, Dept Chem Phys, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Chem React Dynam, Dalian 116023, Peoples R China
[3] Hefei Natl Lab, Hefei 230088, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Liaoning Normal Univ, Interdisciplinary Res Ctr Biol & Chem, Dalian 116029, Peoples R China
基金
中国国家自然科学基金;
关键词
CONFORMER-DEPENDENT REACTIVITY; SUBSTITUTED CARBONYL OXIDES; POTENTIAL-ENERGY SURFACES; CRIEGEE INTERMEDIATE; AB-INITIO; ATMOSPHERIC CHEMISTRY; DISSOCIATION DYNAMICS; ISOPRENE OZONOLYSIS; ALKENE OZONOLYSIS; MECHANISM;
D O I
10.1021/acs.jpca.5c00449
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reaction of anti-CH3CHOO with H2O is a crucial atmospheric process, resulting in the end products CH3COOH + H2O through the dissociation of the intermediate hydroxyethyl hydroperoxide (CH3CH(HO)OOH, HEHP). Based on an accurate full-dimensional PES, we have obtained detailed dynamics information for this reaction through quasi-classical trajectory simulations. We report two reaction mechanisms for the CH3COOH + H2O product channel: one involving a direct mechanism through the transition state and the other an intriguing OH roaming mechanism. The roaming pathway proceeds via the dissociation of HEHP into OH and the hydroxyethoxy radical (CH3CH(HO)O, HEO), where the OH radical roams near HEO and abstracts a hydrogen atom, subsequently forming H2O and CH3COOH. The presence of this roaming pathway significantly increases the yield of CH3COOH + H2O. This work provides new dynamical support for the study of the anti-CH3CHOO + H2O reaction and enriches our understanding of atmospheric chemistry.
引用
收藏
页码:4364 / 4373
页数:10
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