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• W2020046645 abstract "The kinetics of the reaction of the CH3CHBr, CHBr2 or CDBr2 radicals, R, with HBr have been investigated in a temperature-controlled tubular reactor coupled to a photoionization mass spectrometer. The CH3CHBr (or CHBr2 or CDBr2) radical was produced homogeneously in the reactor by a pulsed 248 nm exciplex laser photolysis of CH3CHBr2 (or CHBr3 or CDBr3). The decay of R was monitored as a function of HBr concentration under pseudo-first-order conditions to determine the rate constants as a function of temperature. The reactions were studied separately from 253 to 344 K (CH3CHBr + HBr) and from 288 to 477 K (CHBr2 + HBr) and in these temperature ranges the rate constants determined were fitted to an Arrhenius expression (error limits stated are 1σ + Student’s t values, units in cm3 molecule−1 s−1, no error limits for the third reaction): k(CH3CHBr + HBr) = (1.7 ± 1.2) × 10−13 exp[+ (5.1 ± 1.9) kJ mol−1/RT], k(CHBr2 + HBr) = (2.5 ± 1.2) × 10−13 exp[−(4.04 ± 1.14) kJ mol−1/RT] and k(CDBr2 + HBr) = 1.6 × 10−13 exp(−2.1 kJ mol−1/RT). The energy barriers of the reverse reactions were taken from the literature. The enthalpy of formation values of the CH3CHBr and CHBr2 radicals and an experimental entropy value at 298 K for the CH3CHBr radical were obtained using a second-law method. The result for the entropy value for the CH3CHBr radical is 305 ± 9 J K−1 mol−1. The results for the enthalpy of formation values at 298 K are (in kJ mol−1): 133.4 ± 3.4 (CH3CHBr) and 199.1 ± 2.7 (CHBr2), and for α-C–H bond dissociation energies of analogous compounds are (in kJ mol−1): 415.0 ± 2.7 (CH3CH2Br) and 412.6 ± 2.7 (CH2Br2), respectively." @default.
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• W2020046645 date "2008-07-01" @default.
• W2020046645 modified "2023-09-24" @default.
• W2020046645 title "Kinetics of the R+HBr⇄RH+Br (CH3CHBr, CHBr2 or CDBr2) equilibrium. Thermochemistry of the CH3CHBr and CHBr2 radicals" @default.
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• W2020046645 doi "https://doi.org/10.1016/j.chemphys.2008.04.008" @default.
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