THE SPIN-FORBIDDEN A (4)PI(NU=13-15) AND B(4)SIGMA(-)(NU=3)[-X(2)PI(NU=0) BANDS OF NITRIC-OXIDE - A NEW SCHEME FOR QUANTUM STATE-SPECIFIC HIGH-RESOLUTION KINETIC-ENERGY MEASUREMENTS
M. Drabbels et al., THE SPIN-FORBIDDEN A (4)PI(NU=13-15) AND B(4)SIGMA(-)(NU=3)[-X(2)PI(NU=0) BANDS OF NITRIC-OXIDE - A NEW SCHEME FOR QUANTUM STATE-SPECIFIC HIGH-RESOLUTION KINETIC-ENERGY MEASUREMENTS, The Journal of chemical physics, 103(18), 1995, pp. 7700-7707
A new scheme for performing high-resolution kinetic energy measurement
s on single quantum states of NO is described. Laser excitation of the
a (4) Pi(nu=13-15) and b 4 Sigma(-)(nu= 3)<--X (2) Pi(v=0) spin-forbi
dden bands has been used to produce NO a (4) Pi, either by direct exci
tation or after excitation to NO b (4) Sigma(-) followed by b-->a emis
sion. The sensitivity is compared to previous experiments on CO, emplo
ying the forbidden Cameron system. In the course of these experiments,
three previously unknown vibronic levels of the a (4) Pi state were o
bserved for which high precision molecular constants have been obtaine
d. The derived molecular constants have been used to construct a chemi
cally accurate RKR potential for the a (4) Pi state to within 0.2 eV o
f the dissociation limit. In addition, the electric dipole moments for
the a (4) Pi(nu=13-14) levels have been determined. By comparing the
experimental results with two ab initio calculations, the polarity of
the dipole moment of the a (4) Pi State at equilibrium separation coul
d be determined. A set of supplementary molecular beam laser-induced f
luorescence studies on the b (4) Sigma(-)(v=3)<--X (2) Pi(nu=0) band w
ere also carried out. These allowed the fluorescence lifetime of b (4)
Sigma(-)(nu=3) state to be obtained under collision-free conditions a
nd the electronic origin of the quartet manifold to be determined with
in 0.03 cm(-1). (C) 1995 American Institute of Physics.