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Formation Of Dimethylketene And Methacrolein By Reaction Of The Ch Radical With Acetone, Fabien Goulay, Adeeb Derakhshan, Eamonn Maher, Adam J. Trevitt, John D. Savee, Adam M. Scheer, David L. Osborn, Craig A. Taatjes
Formation Of Dimethylketene And Methacrolein By Reaction Of The Ch Radical With Acetone, Fabien Goulay, Adeeb Derakhshan, Eamonn Maher, Adam J. Trevitt, John D. Savee, Adam M. Scheer, David L. Osborn, Craig A. Taatjes
Adam Trevitt
The reaction of the methylidyne radical (CH) with acetone ((CH3)2CO) is studied at room temperature and at a pressure of 4 Torr (533.3 Pa) using a multiplexed photoionization mass spectrometer coupled to the tunable vacuum ultraviolet synchrotron radiation of the Advanced Light Source at Lawrence Berkeley National Laboratory. The CH radicals are generated by 248 nm multiphoton photolysis of bromoform and react with acetone in an excess of helium and nitrogen gas flow. The main observed reaction exit channel is elimination of a hydrogen atom to form C4H6O isomers. Analysis of photoionization spectra identifies dimethylketene and methacrolein as the only …