TRANSITION-STATE SPECTROSCOPY VIA NEGATIVE-ION PHOTODETACHMENT

被引:191
作者
NEUMARK, DM [1 ]
机构
[1] LAWRENCE BERKELEY LAB, DIV CHEM SCI, BERKELEY, CA 94720 USA
关键词
D O I
10.1021/ar00026a001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this Account, we have briefly described three examples in which negative ion photodetachment is used to probe the transition-state region of a bimolecular reaction. The examples illustrate that photoelectron spectroscopy and threshold photodetachment spectroscopy can yield vibrational structure and dissociation dynamics associated with the transition state. The three examples also show the importance of anion geometry, as this determines which region of the neutral potential energy surface is accessible via photodetachment. This last point is, in fact, one of the most important limitations of these experiments. One way to mitigate this problem is to perform photoelectron spectroscopy studies on vibrationally excited anions. Photodetachment of these anions will probe different vibrational levels and geometries of the neutral transition state. Such studies are planned for the near future. © 1993, American Chemical Society. All rights reserved.
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收藏
页码:33 / 39
页数:7
相关论文
共 53 条
[21]   CHEMICAL-DYNAMICS STUDIED BY EMISSION-SPECTROSCOPY OF DISSOCIATING MOLECULES [J].
IMRE, D ;
KINSEY, JL ;
SINHA, A ;
KRENOS, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (18) :3956-3964
[22]   SPECTROSCOPIC CHARACTERIZATION OF REPULSIVE POTENTIAL-ENERGY SURFACES - FLUORESCENCE-SPECTRUM OF OZONE [J].
IMRE, DG ;
KINSEY, JL ;
FIELD, RW ;
KATAYAMA, DH .
JOURNAL OF PHYSICAL CHEMISTRY, 1982, 86 (14) :2564-2566
[23]   HIGH-RESOLUTION THRESHOLD PHOTODETACHMENT SPECTROSCOPY OF NEGATIVE-IONS [J].
KITSOPOULOS, TN ;
WALLER, IM ;
LOESER, JG ;
NEUMARK, DM .
CHEMICAL PHYSICS LETTERS, 1989, 159 (04) :300-306
[24]   REACTIVE COLLISION DYNAMICS BY FAR WING LASER SCATTERING - MG + H2 [J].
KLEIBER, PD ;
LYYRA, AM ;
SANDO, KM ;
ZAFIROPULOS, V ;
STWALLEY, WC .
JOURNAL OF CHEMICAL PHYSICS, 1986, 85 (10) :5493-5504
[25]   A FOURIER METHOD SOLUTION FOR THE TIME-DEPENDENT SCHRODINGER-EQUATION AS A TOOL IN MOLECULAR-DYNAMICS [J].
KOSLOFF, D ;
KOSLOFF, R .
JOURNAL OF COMPUTATIONAL PHYSICS, 1983, 52 (01) :35-53
[26]   ASSIGNMENT OF PEAKS IN PHOTODETACHMENT SPECTRA USING PREDICTED DENSITIES OF REACTIVE STATES - APPLICATION TO H2F AND DF2 [J].
KRESS, JD ;
HAYES, EF .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (07) :4881-4889
[27]   RESONANCES IN REACTIVE COLLISIONS - COMPUTATIONAL STUDY OF H+H2 COLLISION [J].
LEVINE, RD ;
WU, SF .
CHEMICAL PHYSICS LETTERS, 1971, 11 (05) :557-+
[28]  
LEVINE RD, 1987, MOL REACTION DYNAMIC, P397
[29]   USE OF SCALED EXTERNAL CORRELATION, A DOUBLE MANY-BODY EXPANSION, AND VARIATIONAL TRANSITION-STATE THEORY TO CALIBRATE A POTENTIAL-ENERGY SURFACE FOR FH2 [J].
LYNCH, GC ;
STECKLER, R ;
SCHWENKE, DW ;
VARANDAS, AJC ;
TRUHLAR, DG ;
GARRETT, BC .
JOURNAL OF CHEMICAL PHYSICS, 1991, 94 (11) :7136-7149
[30]   ON THE COLLINEAR I+HI AND I+MUI REACTIONS [J].
MANZ, J ;
ROMELT, J .
CHEMICAL PHYSICS LETTERS, 1981, 81 (02) :179-184