75-35-4 Laser-induced Decomposition of 1,1,2-Trichloroethane

https://www.lookchem.com/CASDataBase_75-35-4.htm

 CH2ClCHCl2 was photolyzed with a focusing geometry using the P(24) line of the 10.6 μm CO2 band (940.6 cm-1).The final products of neat photolysis were cis- and trans-CHCl=CHCl, CH2=CCl2, CH2=CHCl, CH<*>CCl, CH<*>CH, and C4H2.The relative yield of CH2=CCl2 in particular was strongly dependent on CH2ClCHCl2 pressure and sensitive to the addition of H atom containing molecules.A series of diagnostic experiments shows that the dichloroethene isomers are formed by three different processes, i.e., infrared multiphoton decomposition, collision-induced decomposition, and radical chain reaction.Infrared multiphoton decomposition and collision-induced decomposition give rise to cis- and trans-CHCl=CHCl predominantly, while the radical chain reaction generates the dichloroethane isomers in comparable amounts at high reactant pressures, the most probable initiation step being the C-Cl bond-scission reaction of the parent molecule.Formation mechanisms for other minor products are also discussed. 

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