Quantum mechanical study of the insertion reaction between cyclopropenylidene with r-h (r=f, oh, nh2, ch3)

• YING JING ^[1] ; HUI LIU ^[3] ; HAILONG WANG ^[2] ; YANG YU ^[3] ; XIAOJUN TAN ^[2] ; YUNGANG CHEN ^[2] ; YONGLING ZHANG ^[2] ; JINSONG GU ^[2]
  1. [1] General Hospital of Jinan Military Command

     General Hospital of Jinan Military Command

     China

     
  2. [2] University of Jinan

     University of Jinan

     China

     
  3. [3] Shandong Academy of Medical Sciences

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• Localización: Journal of the Chilean Chemical Society (Boletín de la Sociedad Chilena de Química), ISSN-e 0717-6309, ISSN 0366-1644, Vol. 58, Nº. 4, 2013, págs. 2219-2221
• Idioma: inglés
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  • To further reveal the reactivity of cyclopropenylidene with R-H compounds, mechanisms of four reactions between cyclopropenylidene and R-H (R=F, OH, NH2, CH3) have been systematically investigated employing the second-order Møller-Plesset perturbation theory (MP2) method. Geometry optimization, vibrational analysis, and energy property for the involved stationary points on the potential energy surface have been calculated. All the mechanisms of four reactions are identical to each other. Based on the calculated results, there are three steps (step a, b, and c) along the reaction between cyclopropenylidene and R-H. For the first step, cyclopropenylidene is inserted into R-H to form an three-membered ring intermediate. For the second step, the three-membered ring is opened to form a carbene intermediate. With regard to the third step, it is H-transfered processes, the ultimate product is alkyne.