The gas-phase reaction of the CF3 radical with thiophene

2003 ◽  
Vol 81 (12) ◽  
pp. 1477-1481 ◽  
Author(s):  
Olga S Herrera ◽  
Jorge D Nieto ◽  
Silvia I Lane ◽  
Elena V Oexler

The reaction of CF3 radicals, generated by photolysis of CF3I or hexafluoroacetone with thiophene, was studied in the gas phase at 25 °C. At conversion of thiophene less than 20%, monosubstituted CF3-thiophenes were found as the main reaction products, in addition to CF3H, C2F6, and monosubstituted dihydro-CF3-thiophene, the latter in very low proportion. An isomeric mixture of 2- and 3-CF3-thiophene was obtained in a ratio of about 16, independent of the radical source used (CF3I or hexafluoroacetone) to produce the CF3 radicals. A plausible mechanism that accounts for the observed products is proposed, and the reactivity of thiophene toward the CF3 radical at 25 °C was determined as kadd/kc1/2 = 106 ± 4 cm3/2 mol–1/2 s–1/2.Key words: thiophene, trifluoromethyl radical, reaction mechanism, reactivity.

2015 ◽  
Vol 122 ◽  
pp. 513-520 ◽  
Author(s):  
Jason E. Ham ◽  
Stephen R. Jackson ◽  
Joel C. Harrison ◽  
J.R. Wells

2007 ◽  
Vol 23 (02) ◽  
pp. 217-222
Author(s):  
LIU Le-Yan ◽  
◽  
◽  
GENG Zhi-Yuan ◽  
ZHAO Cun-Yuan ◽  
...  

2019 ◽  
Vol 21 (36) ◽  
pp. 20296-20307 ◽  
Author(s):  
Narcisse T. Tsona ◽  
Shanshan Tang ◽  
Lin Du

The role of water in preventing the barrierless hydrogen abstraction in the BrO + HO2 reaction is highlighted.


2004 ◽  
Vol 676 (1-3) ◽  
pp. 97-103 ◽  
Author(s):  
Annia Galano ◽  
J.Raúl Alvarez-Idaboy ◽  
Esther Agacino-Valdés ◽  
Ma.Esther Ruiz-Santoyo

1993 ◽  
Vol 48 (12) ◽  
pp. 1234-1238 ◽  
Author(s):  
J. Nolte ◽  
J. Grußdorf ◽  
F. Temps ◽  
H. Gg. Wagner

Using the discharge flow method, the kinetics of the gas phase reactionHOCO + O2 products (1)was investigated at room temperature and pressures around p ≈ 2.0 mbar with Far Infrared LaserMagnetic Resonance (FIR-LMR) detection of HOCO, HO2 , and OH. From the measured concentration-versus-time decay profiles of HOCO in the absence and presence of a large excess of O2 , theoverall rate constant of the reaction was found to bek1 (296 K) = (9.9 ±1.5) • 1011 cm3/mol • s.The main reaction channel, which leads to production of HO2 + CO2 , could be established.


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