A GUIDED-ION BEAM STUDY OF THE HYDROGEN-ATOM TRANSFER-REACTION OF STATE-SELECTED N-2(+) WITH H-2 AT COLLISION ENERGIES RANGING FROM SUBTHERMAL TO 2-EV (CM)

被引:14
作者
KNOTT, WJ [1 ]
PROCH, D [1 ]
KOMPA, KL [1 ]
ROSEPETRUCK, C [1 ]
机构
[1] UNIV CALIF SAN DIEGO,DEPT CHEM,LA JOLLA,CA 92093
关键词
D O I
10.1063/1.469394
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This article presents detailed internal and kinetic energy dependent cross sections and reaction rates for the hydrogen atom transfer processes N 2+(X 2Σg+, v + = 0-4, J+ = 2)+H2→N2H + + H, which were obtained under single-collision conditions in a guided-ion beam/scattering gas experiment. Preparation of ions in specific states relied on single-color excitation within a resonantly enhanced (2+1) multiphoton ionization scheme. The translational energy of the ions, E lab, was varied from 0.1 eV to approximately 30 eV. A small activation barrier impedes the reaction. Vibronic state preparation of the nitrogen ion is influential on the nature of the energy surface - N 2++H2 or H2++N 2 - along which the H atom transfer proceeds. Calculations of model potential energy surfaces suggest that the reaction pathway must involve several exoergic and endoergic channels which open successively as the collision energy increases. A purely collision determined cross section-as would be evidenced by the E-1/2 dependence formulated in the Langevin-Gioumousis-Stevenson model - is observed only within a narrow window of kinetic energies. © 1995 American Institute of Physics.
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页码:214 / 225
页数:12
相关论文
共 76 条
[41]   STATE SELECTED ION-MOLECULE REACTIONS BY A TESICO TECHNIQUE .9. VIBRATIONAL-STATE DEPENDENCE OF THE CROSS-SECTIONS IN THE REACTION C2H2+ (NU-2) + D2(H2) [J].
HONMA, K ;
KATO, T ;
TANAKA, K ;
KOYANO, I .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (12) :5666-5671
[42]   VIBRATIONAL EFFECTS IN PROTON AND CHARGE-TRANSFER IN THE H2++AR SYSTEM [J].
HOULE, FA ;
ANDERSON, SL ;
GERLICH, D ;
TURNER, T ;
LEE, YT .
CHEMICAL PHYSICS LETTERS, 1981, 82 (03) :392-395
[43]   A RECONSIDERATION OF THE THEORY OF CAPTURE CROSS-SECTIONS FOR ION-MOLECULE REACTIONS AND A TOTAL ENERGY AND ANGULAR-MOMENTUM CONSERVED AVERAGE CHARGE-DIPOLE INTERACTION THEORY (TEAMS) [J].
HSIEH, ETY ;
CASTLEMAN, AW .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1981, 40 (03) :295-329
[44]  
Huber K. P., 1979, CONSTANTS DIATOMIC M, DOI DOI 10.1007/978-1-4757-0961-2_2
[45]   STATE-SELECTED ION-MOLECULE REACTIONS BY A THRESHOLD ELECTRON-SECONDARY ION COINCIDENCE (TESICO) TECHNIQUE .1. APPARATUS AND THE REACTION H-2+ + H-2-]H-3+ +H [J].
KOYANO, I ;
TANAKA, K .
JOURNAL OF CHEMICAL PHYSICS, 1980, 72 (09) :4858-4868
[46]   STATE-SELECTED CHARGE-TRANSFER AND REARRANGEMENT REACTIONS IN 4-ATOM ION-MOLECULE SYSTEMS [J].
KOYANO, I ;
TANAKA, K ;
KATO, T ;
SUZUKI, S .
FARADAY DISCUSSIONS, 1987, 84 :265-279
[47]   SPECTRUM OF MOLECULAR NITROGEN [J].
LOFTHUS, A ;
KRUPENIE, PH .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1977, 6 (01) :113-307
[48]   VIBRATIONALLY STATE-SELECTED REACTIONS OF AMMONIA IONS .1. NH3+(V)+D2 [J].
MORRISON, RJS ;
CONAWAY, WE ;
EBATA, T ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1986, 84 (10) :5527-5535
[49]   EFFECT OF INTERNAL AND TRANSLATIONAL ENERGY ON THE NH3+(UPSILON)+D-2 ION MOLECULE REACTION [J].
MORRISON, RJS ;
CONAWAY, WE ;
ZARE, RN .
CHEMICAL PHYSICS LETTERS, 1985, 113 (05) :435-440
[50]   RESONANT MULTIPHOTON IONIZATION DYNAMICS OF N2 VIA THE A 1-PI-G(V=10-14) STATES - PREPARATION OF STATE-SELECTED N2+ X2-SIGMA-G+(V+=0-4) IONS [J].
ONDREY, GS ;
ROSE, C ;
PROCH, D ;
KOMPA, KL .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (11) :7823-7827