Journal of Physical Chemistry p. 10815 - 10823 (1995)
Update date:2022-08-11
Topics:
Boyd, A.A.
Noziere, B.
Lesclaux, R.
The equilibrium kinetics of the reversible additions of NO to the benzyl (C6H5CH2) and allyl (CH2CHCH2) radicals have been studied at atmospheric pressure and over the temperature range 400 < T < 520 K.Experiments were performed using a flash photopysis/UV absorption technique with kinetic data being derived from numerical simulation of real-time decays of benzyl and allyl radicals, recorded both with and without the addition of excess nitric oxide.The equilibrium constants were therefore deduced as the ration of the rate coefficients (k1/k-1 and k3/k-3) for the forward and reverse processes: C6H5CH2 + NO + N2 <-> C6H5CH2NO + N2 (reactions 1, -1) and CH2CHCH2 + NO +N2 <=> CH2CHCH2NO + N2 (reactions 3, -3).Thermodynamic treatment of the data by both second law and third law methods of analysis yielded values for the enthalpy and entropy of reaction 1 and 3 which were self consistent and hence the following average values: reaction 1, ΔH0298 = -123 +/- 5 kJ mol-1 (thus ΔH00 = -117 +/- 6 kJ mol-1 and ΔH0f298(C6H5CH2-NO) = 176 +/- 7 kJ mol-1, ΔS0298 = -159 +/- 9 J K-1 mol-1); reaction 3, ΔH0298 = -110 +/- 5 kJ mol-1 (thus ΔH00 = -105 +/- 4 kJ mol-1 and ΔH0f298(CH2CHCH2NO) = 148 +/- 8 kJ mol-1 ΔS0298 = -154 +/- 9 kJ mol-1).The bond dissociation energies for these adducts (= -ΔH0298) are compared and discussed in relation to those for other alkyl nitrosos.Also as part of the study, some measurements of the rate coefficients for the benzyl and ally association reactions with NO (reactions 1 and 3) and their radical self-recombinations (reaction 4, C6H5CH2 + C6H5CH2, and reaction 5, CH2CHCH2 + CH2CHCH2) were made under similar experimental conditions, yielding (in units 1E-11 cm3 molecule-1 s-1): k1(415, 443, 466 K) = 0.91 +/- 0.08, 0.81 +/- 0.05, and 0.62 +/- 0.09, k3(403 K) = 0.71 +/- 0.04, k4(435-519 K) = 2.9 +/- 0.3, k5(403-540 K) = 2.6 +/- 0.2.
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