The gas phase reactions of hydroxyl radicals with a series of nitroalkanes over the temperature range 240-400 K
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The gas phase reactions of hydroxyl radicals with a series of nitroalkanes over the temperature range 240-400 K. / Liu, Renzhang; Huie, Robert E.; Kurylo, Michael J.; Nielsen, Ole J.
In: Chemical Physics Letters, Vol. 167, No. 6, 13.04.1990, p. 519-523.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - The gas phase reactions of hydroxyl radicals with a series of nitroalkanes over the temperature range 240-400 K
AU - Liu, Renzhang
AU - Huie, Robert E.
AU - Kurylo, Michael J.
AU - Nielsen, Ole J.
PY - 1990/4/13
Y1 - 1990/4/13
N2 - Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of nitroalkanes by the flash photolysis-resonance fluorescence technique. Experiments were performed at total pressures from 25 to 50 Torr using Ar as a diluent gas. Experiments with nitromethane and nitromethane-d3 at 296 K yielded rate constants of (1.58±0.09) × 10-14 and (0.9±0.04) × 10-14 cm3 molecule-1 s-1, respectively. Data from experiments over the temperature range 240-400 K for nitroethane, 1-nitropropane, 2-nitropropane, 1-nitrobutane, and 1-nitropentane were used to evaluate their Arrhenius parameters. The results are discussed in terms of the reaction mechanism, and are compared to previous literature data.
AB - Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of nitroalkanes by the flash photolysis-resonance fluorescence technique. Experiments were performed at total pressures from 25 to 50 Torr using Ar as a diluent gas. Experiments with nitromethane and nitromethane-d3 at 296 K yielded rate constants of (1.58±0.09) × 10-14 and (0.9±0.04) × 10-14 cm3 molecule-1 s-1, respectively. Data from experiments over the temperature range 240-400 K for nitroethane, 1-nitropropane, 2-nitropropane, 1-nitrobutane, and 1-nitropentane were used to evaluate their Arrhenius parameters. The results are discussed in terms of the reaction mechanism, and are compared to previous literature data.
UR - http://www.scopus.com/inward/record.url?scp=33646916037&partnerID=8YFLogxK
U2 - 10.1016/0009-2614(90)85462-L
DO - 10.1016/0009-2614(90)85462-L
M3 - Journal article
AN - SCOPUS:33646916037
VL - 167
SP - 519
EP - 523
JO - Chemical Physics Letters
JF - Chemical Physics Letters
SN - 0009-2614
IS - 6
ER -
ID: 228197883