Acta Chimica Sinica ›› 2006, Vol. 64 ›› Issue (9): 868-872. Previous Articles     Next Articles

Original Articles

单嘧磺隆除草剂水解机理的理论研究

廖显威*,1,邓嘉莉1,李来才1,苏宇2,范志金3   

  1. (1四川师范大学化学学院 成都 610066)
    (2川北医学院化学教研室 四川 南充 637007)
    (3南开大学元素有机化学国家重点实验室 天津 300071)
  • 投稿日期:2005-01-14 修回日期:2006-01-14 发布日期:2006-05-15
  • 通讯作者: 廖显威

Theoretical Study on the Hydrolysis Mechanism of Monosulfuron Herbicide

LIAO Xian-Wei*,1, DENG Jia-Li1, LI Lai-Cai1, SU Yu2, FAN Zhi-Jin3   

  1. (1 College of Chemistry, Sichuan Normal University, Chengdu 610066)
    (2 Teaching and Research Group of Chemistry, Sichuan North Medical College, Nanchong 637007)
    (3 State Key Laboratory of Elemental Organic Chemistry, Nankai University, Tianjin 300071)
  • Received:2005-01-14 Revised:2006-01-14 Published:2006-05-15
  • Contact: LIAO Xian-Wei

In this paper, the hydrolysis mechanism of monosulfuron herbicide was studied by B3LYP method at the level of 6-31G*. The geometric configurations of reactants, products, intermediates, and transition states in the reaction have been optimized and vibrational analysis has been performed. The results of calculation show that in the basicity, the reaction channel has one five-membered ring transition state TS1, with the activation energy of the controlling step during the reaction of 25.7 kJ/mol, while in the neutrality, the reaction channel has one three-membered and two four-membered ring transition states, and the controlling step is M3'+H2O→TS2' during the reaction with the activation energy of 236.5 kJ/mol. That is to say, the hydrolysis reaction of monosulfuron herbicide proceeded more easily in the basicity than neutrality, which is essentially consistent with the experimental result. Besides, the influence of the solvation effect was also discussed.

Key words: monosulfuron, hydrolysis mechanism, basicity, neutrality