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Titolo: Rate constants for the reactions of chlorine atoms with deuterated methanes: Experiment and theory
Autore: Boone, GD; Agyin, F; Robichaud, DJ; Tao, FM; Hewitt, SA;
 Indirizzi:
 Calif State Univ Fullerton, Dept Chem & Biochem, Fullerton, CA 92834 USA Calif State Univ Fullerton Fullerton CA USA 92834 Fullerton, CA 92834 USA
 Titolo Testata:
 JOURNAL OF PHYSICAL CHEMISTRY A
fascicolo: 9,
volume: 105,
anno: 2001,
pagine: 1456  1464
 SICI:
 10895639(20010308)105:9<1456:RCFTRO>2.0.ZU;2I
 Fonte:
 ISI
 Lingua:
 ENG
 Soggetto:
 POTENTIALENERGY SURFACE; LOWER ANTARCTIC STRATOSPHERE; LARGE (CO)C13 DEFICIT; OZONE HOLE CHEMISTRY; ATMOSPHERIC CH4; RATE COEFFICIENTS; ABINITIO; ISOTOPE; CL; CH3D;
 Tipo documento:
 Article
 Natura:
 Periodico
 Settore Disciplinare:
 Physical, Chemical & Earth Sciences
 Citazioni:
 48
 Recensione:
 Indirizzi per estratti:
 Indirizzo: Hewitt, SA Calif State Univ Fullerton, Dept Chem & Biochem, Fullerton, CA 92834 USA Calif State Univ Fullerton Fullerton CA USA 92834 CA 92834 USA



 Citazione:
 G.D. Boone et al., "Rate constants for the reactions of chlorine atoms with deuterated methanes: Experiment and theory", J PHYS CH A, 105(9), 2001, pp. 14561464
Abstract
Longpath FTIR spectroscopy and ab initio calculations combined with conventional transition state theory were used to study the kinetics of the reactions of Cl atoms with deuterated methanes. The following experimental relative rate constants for the reaction of Cl atoms at 298 +/ 5 K and 760 +/5 Torr were determined: CH3D, (6.5 +/ 0.5) x 10(14); CH2D2, (4.2 +/ 0.5) x 10(14); CHD3, (1.9 +/ 0.3) x 10(14); CD4, (5.4 +/ 0.4) x 10(15). All experimental and theoretical rate constants are in units of cm(3) molecule(1) s(1) and are relative to the 1.0 x 10(13) cm(3) molecule(1) s(1)rate constant for the reaction of Cl with CH4. All experimental uncertainty limits are 2 sigma. The geometries, energies, and frequencies of the reactants, products, and transition states were calculated at the level of the secondorder MollerPlesset approximation using a 6311++G(2d,2p) basis set. The following theoretical relative rate constants were calculated at 298K using conventional transition state theory combined with an Eckart onedimensional tunneling correction: CH3D, 6.8 x 10(14); CH2D2, 4.2 x 10(14);CHD3, 2.1 x 10(14); CD4, 4.4 x 10(15). The theoretical rate constants agree well with the experimental results. The curvature in both the experimental and theoretical rate constants as a function of deuteration is due to asecondary kinetic isotope effect, involving mainly the rate constant preexponential factors. The large decrease in Cl atom rate constant in going from CH4 to CH3D (i.e., the increase in curvature at CH3D) is due to the reduced symmetry in the transition state and a massdependent effect. The implications for previous studies, atmospheric chemistry, and chemical reactivityare discussed.
ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/20 alle ore 17:02:54