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电子激发态CCl2自由基被H2O猝灭的研究

Ab INITIO CALCULATIONS ON THE REACTION MECHANISM FOR THE CCl2 WITH H2O AND QUENCHING OF CCl2(A1B1 AND a3B1) BY H2O

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【作者】 高义德刘云珍陈晹陈从香

【Author】 GAO Yi de, LIU Yun zhen, CHEN Yang, CHEN Cong xiang (Open Laboratory of Bond Selective Chemistry, Department of Chemical Physics, University of Science and Technology of China, Hefei, Anhui, 230026,China )

【机构】 中国科学院选键化学开放实验室!中国科学技术大学化学物理系安徽合肥230026中国科学院选键化学开放实验室!中国科学技术?

【摘要】 对CCl4 /Ar混合气体直流脉冲放电产生CCl2 自由基 ,再用 541.52nm激光将电子基态CCl2激励到激发态A1B1( 0 ,4 ,0 )振动态的K =0能级上 ,通过检测激发态CCl2 时间分辨荧光信号 ,测得室温下CCl2 (A1B1和a3B1)被H2 O分子猝灭的实验结果 ,用三能级模型分析处理实验数据 ,获得态分辨速率常数KA 和Ka 值 .利用UMP2 (Full) / 6- 31G(d ,p)方法计算了该反应的势能面 ,揭示了反应的插入和加成 -消除机理

【Abstract】 CCl 2 free radicals were produced by dc discharge of CCl 4(in Ar). Ground electronic state CCl 2 radical was electronically excited to A 1B 1 (0,4,0) state K=0 level with Nd:YAG laser pumped dye laser at 541.52 nm. Experimental quenching data of CCl 2 (A 1B 1 and a 3B 1) by H 2O were obtained by observing time resolved fluorescence from the excited CCl 2 radicals transition, which showed a superposition of two exponential decay components. The state-resolved rate constants K A and Ka were acquired by analyzing and dealing with these data by using three-level-model, which was put forward by us. The extensive potential energy surface (PES) for CCl 2 with H 2O has been studied using the UMP 2(full)/6-31G(d, P). The addition-elimination reaction mechanism is revealed.

【基金】 国家自然科学基金重点项目!(10 0 32 0 5 0 );国家自然科学基金项目!(2 99730 38);中国科学院重大项目!(HH0 30 30 1);国家重点基
  • 【文献出处】 安徽师范大学学报(自然科学版) ,Journal of Anhui Normal University(Natural Science) , 编辑部邮箱 ,2001年02期
  • 【分类号】O621
  • 【下载频次】23
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