Kinetics of the gas-phase reactions of NO3 radicals with a series of alcohols, glycol ethers, ethers and chloroalkenes. Chew, A., A., Atkinson, R., & Aschmann, S., M. Journal of the Chemical Society-Faraday Transactions, 94(8):1083-1089, 1998.
abstract   bibtex   
Using a relative rate method, rate constants have been measured for the gas-phase reactions of the NO3 radical with methacrolein, a series of ethers, glycol ethers, alcohols and chloroalkenes at 298 +/- 2 K and atmospheric pressure of air. The rate constants determined tin units of 10(-16) cm(3) molecule(-1) s(-1)) were: methacrolein, 33 +/- 10; diethyl ether, 31 +/- 10; di-n-propyl ether, 49 +/- 16; diisopropyl ether, 40 +/- 13; ethyl tert-butyl ether, 45 +/- 14; 1- methoxypropan-2-ol, less than or equal to 15 +/- 5; 2- butoxyethanol, less than or equal to 31 +/- 11; propan-1-ol, less than or equal to 21 +/- 8; propan-2-ol, less than or equal to 17 +/- 6; butan-1-ol, less than or equal to 27 +/- 10; butan-2-ol, less than or equal to 25 +/- 8; heptan-4-ol, less than or equal to 60 +/- 20; cis-1,2-dichloroethene, 1.3 +/- 1.3; 1,1-dichloroethene, 18(-6)(+9); trichloroethene, 3.6(- 1.5)(+2.0); tetrachloroethene, <1.8; and 3-chloropropene, 5.8(- 2.0)(+3.0). Carbonyl products of the alcohol reactions arising after H-atom abstraction at the carbon atom to which the -OH group is attached were observed, and rate constants for this reaction pathway obtained. Significant discrepancies with the literature concern propan-2-ol, ethyl tert-butyl ether and 3- chloropropene, with our relative rate constants for these compounds being factors of ca. 2, ca. 2, and ca. 8 lower, respectively, than previously reported absolute rate constant determinations.
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 title = {Kinetics of the gas-phase reactions of NO3 radicals with a series of alcohols, glycol ethers, ethers and chloroalkenes},
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 year = {1998},
 pages = {1083-1089},
 volume = {94},
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 abstract = {Using a relative rate method, rate constants have been measured for the gas-phase reactions of the NO3 radical with methacrolein, a series of ethers, glycol ethers, alcohols and chloroalkenes at 298 +/- 2 K and atmospheric pressure of air. The rate constants determined tin units of 10(-16) cm(3) molecule(-1) s(-1)) were: methacrolein, 33 +/- 10; diethyl ether, 31 +/- 10; di-n-propyl ether, 49 +/- 16; diisopropyl ether, 40 +/- 13; ethyl tert-butyl ether, 45 +/- 14; 1- methoxypropan-2-ol, less than or equal to 15 +/- 5; 2- butoxyethanol, less than or equal to 31 +/- 11; propan-1-ol, less than or equal to 21 +/- 8; propan-2-ol, less than or equal to 17 +/- 6; butan-1-ol, less than or equal to 27 +/- 10; butan-2-ol, less than or equal to 25 +/- 8; heptan-4-ol, less than or equal to 60 +/- 20; cis-1,2-dichloroethene, 1.3 +/- 1.3; 1,1-dichloroethene, 18(-6)(+9); trichloroethene, 3.6(- 1.5)(+2.0); tetrachloroethene, <1.8; and 3-chloropropene, 5.8(- 2.0)(+3.0). Carbonyl products of the alcohol reactions arising after H-atom abstraction at the carbon atom to which the -OH group is attached were observed, and rate constants for this reaction pathway obtained. Significant discrepancies with the literature concern propan-2-ol, ethyl tert-butyl ether and 3- chloropropene, with our relative rate constants for these compounds being factors of ca. 2, ca. 2, and ca. 8 lower, respectively, than previously reported absolute rate constant determinations.},
 bibtype = {article},
 author = {Chew, A A and Atkinson, R and Aschmann, S M},
 journal = {Journal of the Chemical Society-Faraday Transactions},
 number = {8}
}
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