Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene

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Standard

Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene. / Sokolov, O.; Hurley, M. D.; Wellington, T. J.; Kaiser, E. W.; Platz, J.; Nielsen, O. J.; Berho, F.; Rayez, M. T.; Lesclaux, R.

I: Journal of Physical Chemistry A, Bind 102, Nr. 52, 24.12.1998, s. 10671-10681.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Sokolov, O, Hurley, MD, Wellington, TJ, Kaiser, EW, Platz, J, Nielsen, OJ, Berho, F, Rayez, MT & Lesclaux, R 1998, 'Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene', Journal of Physical Chemistry A, bind 102, nr. 52, s. 10671-10681. https://doi.org/10.1021/jp9828080

APA

Sokolov, O., Hurley, M. D., Wellington, T. J., Kaiser, E. W., Platz, J., Nielsen, O. J., Berho, F., Rayez, M. T., & Lesclaux, R. (1998). Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene. Journal of Physical Chemistry A, 102(52), 10671-10681. https://doi.org/10.1021/jp9828080

Vancouver

Sokolov O, Hurley MD, Wellington TJ, Kaiser EW, Platz J, Nielsen OJ o.a. Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene. Journal of Physical Chemistry A. 1998 dec. 24;102(52):10671-10681. https://doi.org/10.1021/jp9828080

Author

Sokolov, O. ; Hurley, M. D. ; Wellington, T. J. ; Kaiser, E. W. ; Platz, J. ; Nielsen, O. J. ; Berho, F. ; Rayez, M. T. ; Lesclaux, R. / Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene. I: Journal of Physical Chemistry A. 1998 ; Bind 102, Nr. 52. s. 10671-10681.

Bibtex

@article{60a66875c443428d9044fb38b03dc89e,
title = "Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene",
abstract = "The gas-phase reaction of Cl atoms with benzene has been studied using both experimental and computational methods. The bulk of the kinetic data were obtained using steady-state photolysis of mixtures containing Cl2, C6H6, and a reference compound in 120-700 Torr of N2 diluent at 296 K. Reaction of Cl atoms with C6H6 proceeds via two pathways; (a) H-atom abstraction and (b) adduct formation. At 296 K the rate constant for the abstraction channel is k1a = (1.3 ± 1.0) × 10-16 cm3 molecule-1 s-1. Phenyl radicals produced via H-atom abstraction from C6H6 react with Cl2 to give chlorobenzene. The main fate of the C6H6-Cl adduct is decomposition to reform C6H6 and Cl atoms. A small fraction of the C6H6-Cl adduct undergoes reaction with Cl atoms via a mechanism which does not lead to the production of C6H5Cl, or the reformation of C6H6. As the steady-state Cl atom concentration is increased, the fraction of the C6H6-Cl adduct undergoing reaction with Cl atoms increases causing an increase in the effective rate constant for benzene removal and a decrease in the chlorobenzene yield. Thermodynamic calculations show that a rapid equilibrium is established between Cl atoms, C6H6, and the C6H6-Cl adduct, and it is estimated that at 296 K the equilibrium constant is Kc,1b = [C6H6-Cl]/[C6H6][Cl] and lies in the range (1-2) × 10-18 cm3 molecule.1 Flash photolysis experiments conducted using C6H6/Cl2 mixtures in 760 Torr of either N2 or O2 diluent at 296 K did not reveal any significant transient UV absorption; this is entirely consistent with results from the steady-state experiments and the thermodynamic calculations. The C6H6-Cl adduct reacts slowly (if at all) with O2 and an upper limit of k(C6H6-Cl + O2) < 8 × 10-17 cm3 molecule-1 s-1 was established. As part of this work a value of k(Cl + CF2ClH) = (1.7 ± 0.1) × 10-15 cm3 molecule-1 s-1 was measured. These results are discussed with respect to the available literature concerning the reaction of Cl atoms with benzene.",
author = "O. Sokolov and Hurley, {M. D.} and Wellington, {T. J.} and Kaiser, {E. W.} and J. Platz and Nielsen, {O. J.} and F. Berho and Rayez, {M. T.} and R. Lesclaux",
year = "1998",
month = dec,
day = "24",
doi = "10.1021/jp9828080",
language = "English",
volume = "102",
pages = "10671--10681",
journal = "Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory",
issn = "1089-5639",
publisher = "American Chemical Society",
number = "52",

}

RIS

TY - JOUR

T1 - Kinetics and mechanism of the gas-phase reaction of Cl atoms with benzene

AU - Sokolov, O.

AU - Hurley, M. D.

AU - Wellington, T. J.

AU - Kaiser, E. W.

AU - Platz, J.

AU - Nielsen, O. J.

AU - Berho, F.

AU - Rayez, M. T.

AU - Lesclaux, R.

PY - 1998/12/24

Y1 - 1998/12/24

N2 - The gas-phase reaction of Cl atoms with benzene has been studied using both experimental and computational methods. The bulk of the kinetic data were obtained using steady-state photolysis of mixtures containing Cl2, C6H6, and a reference compound in 120-700 Torr of N2 diluent at 296 K. Reaction of Cl atoms with C6H6 proceeds via two pathways; (a) H-atom abstraction and (b) adduct formation. At 296 K the rate constant for the abstraction channel is k1a = (1.3 ± 1.0) × 10-16 cm3 molecule-1 s-1. Phenyl radicals produced via H-atom abstraction from C6H6 react with Cl2 to give chlorobenzene. The main fate of the C6H6-Cl adduct is decomposition to reform C6H6 and Cl atoms. A small fraction of the C6H6-Cl adduct undergoes reaction with Cl atoms via a mechanism which does not lead to the production of C6H5Cl, or the reformation of C6H6. As the steady-state Cl atom concentration is increased, the fraction of the C6H6-Cl adduct undergoing reaction with Cl atoms increases causing an increase in the effective rate constant for benzene removal and a decrease in the chlorobenzene yield. Thermodynamic calculations show that a rapid equilibrium is established between Cl atoms, C6H6, and the C6H6-Cl adduct, and it is estimated that at 296 K the equilibrium constant is Kc,1b = [C6H6-Cl]/[C6H6][Cl] and lies in the range (1-2) × 10-18 cm3 molecule.1 Flash photolysis experiments conducted using C6H6/Cl2 mixtures in 760 Torr of either N2 or O2 diluent at 296 K did not reveal any significant transient UV absorption; this is entirely consistent with results from the steady-state experiments and the thermodynamic calculations. The C6H6-Cl adduct reacts slowly (if at all) with O2 and an upper limit of k(C6H6-Cl + O2) < 8 × 10-17 cm3 molecule-1 s-1 was established. As part of this work a value of k(Cl + CF2ClH) = (1.7 ± 0.1) × 10-15 cm3 molecule-1 s-1 was measured. These results are discussed with respect to the available literature concerning the reaction of Cl atoms with benzene.

AB - The gas-phase reaction of Cl atoms with benzene has been studied using both experimental and computational methods. The bulk of the kinetic data were obtained using steady-state photolysis of mixtures containing Cl2, C6H6, and a reference compound in 120-700 Torr of N2 diluent at 296 K. Reaction of Cl atoms with C6H6 proceeds via two pathways; (a) H-atom abstraction and (b) adduct formation. At 296 K the rate constant for the abstraction channel is k1a = (1.3 ± 1.0) × 10-16 cm3 molecule-1 s-1. Phenyl radicals produced via H-atom abstraction from C6H6 react with Cl2 to give chlorobenzene. The main fate of the C6H6-Cl adduct is decomposition to reform C6H6 and Cl atoms. A small fraction of the C6H6-Cl adduct undergoes reaction with Cl atoms via a mechanism which does not lead to the production of C6H5Cl, or the reformation of C6H6. As the steady-state Cl atom concentration is increased, the fraction of the C6H6-Cl adduct undergoing reaction with Cl atoms increases causing an increase in the effective rate constant for benzene removal and a decrease in the chlorobenzene yield. Thermodynamic calculations show that a rapid equilibrium is established between Cl atoms, C6H6, and the C6H6-Cl adduct, and it is estimated that at 296 K the equilibrium constant is Kc,1b = [C6H6-Cl]/[C6H6][Cl] and lies in the range (1-2) × 10-18 cm3 molecule.1 Flash photolysis experiments conducted using C6H6/Cl2 mixtures in 760 Torr of either N2 or O2 diluent at 296 K did not reveal any significant transient UV absorption; this is entirely consistent with results from the steady-state experiments and the thermodynamic calculations. The C6H6-Cl adduct reacts slowly (if at all) with O2 and an upper limit of k(C6H6-Cl + O2) < 8 × 10-17 cm3 molecule-1 s-1 was established. As part of this work a value of k(Cl + CF2ClH) = (1.7 ± 0.1) × 10-15 cm3 molecule-1 s-1 was measured. These results are discussed with respect to the available literature concerning the reaction of Cl atoms with benzene.

UR - http://www.scopus.com/inward/record.url?scp=0001168528&partnerID=8YFLogxK

U2 - 10.1021/jp9828080

DO - 10.1021/jp9828080

M3 - Journal article

AN - SCOPUS:0001168528

VL - 102

SP - 10671

EP - 10681

JO - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory

JF - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory

SN - 1089-5639

IS - 52

ER -

ID: 225754002