The binding energy of VXe+

被引:10
作者
Bellert, D [1 ]
Buthelezi, T [1 ]
Dezfulian, K [1 ]
Hayes, T [1 ]
Brucat, PJ [1 ]
机构
[1] UNIV FLORIDA,CTR CHEM PHYS,GAINESVILLE,FL 32611
关键词
D O I
10.1016/0009-2614(96)00848-2
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
The resonant photodissociation spectrum of gas-phase VXe+ is presented. A single prominent electronic transition with a long upper state vibrational progression is observed in the visible. Analysis of the (VXe+)-V-51-Xe-129 data gives T-00, omega(e)', and omega(e)x(e)' as 15613, 107.9 and 0.95 cm(-1), respectively. The diabatic dissociation energy of the upper state, D-0', corresponding to a 3d(3)4s configuration on the metal ion, is found to be 3220+/-50 cm(-1). This is significantly less than the adiabatic dissociation energy of the ground state, D-0 '', corresponding to a 3d(4) configuration of the metal, at 5240+/-50 cm(-1). These observations are compared with other vanadium-ligand ion complexes.
引用
收藏
页码:458 / 464
页数:7
相关论文
共 15 条
[1]   COLLISION-INDUCED DISSOCIATION OF VANADIUM MONOXIDE ION [J].
ARISTOV, N ;
ARMENTROUT, PB .
JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (21) :5135-5140
[2]   SPIN-FORBIDDEN TRANSITIONS IN NIAR+ [J].
ASHER, RL ;
BELLERT, D ;
BUTHELEZI, T ;
BRUCAT, PJ .
CHEMICAL PHYSICS LETTERS, 1994, 228 (06) :599-604
[3]   THE GROUND-STATE OF COAR(+) [J].
ASHER, RL ;
BELLERT, D ;
BUTHELEZI, T ;
BRUCAT, PJ .
CHEMICAL PHYSICS LETTERS, 1994, 227 (03) :277-282
[4]  
Birge RT, 1926, PHYS REV, V28, P0259, DOI 10.1103/PhysRev.28.259
[5]  
Bottcher C. J. F., 1978, THEORY ELECT POLARIZ, VII
[6]  
FISCHBECK HJ, 1987, FORMULAS FACTS CONST
[7]  
HAYES TJ, UNPUB
[8]   DISSOCIATION ENERGIES AND LONG-RANGE POTENTIALS OF DIATOMIC MOLECULES FROM VIBRATIONAL SPACINGS - HALOGENS [J].
LEROY, RJ ;
BERNSTIE.RB .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1971, 37 (01) :109-&
[10]   CHARACTERIZATION OF TRANSITION METAL-RARE-GAS CATIONS - VAR+ AND VKR+ [J].
LESSEN, D ;
BRUCAT, PJ .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (08) :4522-4530