Title of article :
Theoretical study on the reaction mechanism of  + SCX (X = O, S)
Author/Authors :
Zhou، نويسنده , , Guo-Jing and Geng، نويسنده , , Zhiyuan and Liu، نويسنده , , Jia-cheng and Wang، نويسنده , , Yongcheng and Wang، نويسنده , , Xiu-hong and Wu، نويسنده , , Jian-hua and Liu، نويسنده , , Hong-qiang، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
10
From page :
221
To page :
230
Abstract :
Ab initio calculations of the two title reactions have been made to compare reactivities of OCS and CS2 toward a nucleophile, NH 2 - . MP2/6-311++G(d, p) geometry optimizations on the singlet potential energy surface have demonstrated that respective channels start from key intermediates and have revealed that multistep paths give the most favorable products: (1) NH 2 - + OCS → H2NS− + CO; (2) NH 2 - + OCS → HS− + HNCO; (3) NH 2 - + OCS → NCS− + H2O; (4) NH 2 - + OCS → NCO− + H2S; (5) NH 2 - + CS2 → NCS− + H2S; (6) NH 2 - + CS2 → HS− + HNCS. Furthermore, to get more reliable energetic data, single-point calculations are carried out at CCSD/6-311++G(d, p) level. The calculated result is consistent with the measured large rate constant in experiment. A comparison of reaction mechanisms is offered between NH 2 - + OCS and NH 2 - + CS2.
Keywords :
CS2 , Reaction Mechanism , OCS , NH 2 -
Journal title :
Computational and Theoretical Chemistry
Serial Year :
2011
Journal title :
Computational and Theoretical Chemistry
Record number :
2284820
Link To Document :
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