Title of article :
Experimental and theoretical studies of the CCl + O2 reaction
Author/Authors :
Xiang، نويسنده , , Tiancheng and Liu، نويسنده , , Kunhui and Shi، نويسنده , , Congyun and Su، نويسنده , , Hongmei and Kong، نويسنده , , Fanao، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
6
From page :
8
To page :
13
Abstract :
Elementary reaction of CCl radical with oxygen molecule has been investigated by time-resolved Fourier transform infrared emission spectroscopy. Product of CO was observed. The rate constant of this reaction is measured to be 2.6(±0.4) × 10−12 cm3 molecule−1 s−1. It is found that the nascent product of CO is highly vibrationally excited with an average vibrational energy of 17–18 kcal mol−1. DFT calculations at the B3LYP/6-311G(d) level reveal the reaction mechanism to be mainly a barrierless addition of O2 to CCl leading to a peroxide intermediate IM1 (ClCOO). The chain-like IM1 breaks its O–O bond and Cl–C bond sequentially, forming the product of CO.
Journal title :
Chemical Physics Letters
Serial Year :
2007
Journal title :
Chemical Physics Letters
Record number :
1921442
Link To Document :
بازگشت