Abstract
The Army uses nitrated compounds as explosives and propellants. The ability to selectively nitrate materials is a much-needed process. Laser-induced chemistry possesses the potential to drive some reactions in an efficient and selective manner. Laser-induced chemistry may be useful in driving nitration reactions toward specific products. Reported herein are the results of several successful attempts to laser-induce the reaction of nitrogen dioxide with hydrocarbons of 3,4, and 5 carbons. Specifically, the tunable continuous wave (cw) infrared laser was used to drive the reaction between nitrogen dioxide, NO<sub>2</sub>, and propane, <i>n</i>-butane, isobutane, and <i>n</i>-pentane. The major products of the reactions were secondary (tertiary in the isobutane reaction) nitrohydrocarbons, of the same chain length as the reacting hydrocarbon. Some short-chain nitrated compounds were also identified. The yield of 2-nitrobutane observed in the nitration of butane is ~20% on the basis of the depletion of NO<sub>2</sub>. The propane reacted with NO<sub>2</sub> to produce mostly 2-nitropropane with a smaller yield of 5-9%. The analogous reaction of pentane produced ~9% of the major product, which is believed to be 2-nitropentane. The isobutane nitration resulted in approximately a 10% yield of 2-methyl-2-nitropropane. The results of these laser-induced reactions are contrasted to the corresponding thermal reactions. The reaction mechanism is also discussed for these two processes.
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