15min:
THE OPTICAL STARK SPECTRUM OF THE A3 Phi4-X3 Phi4 BAND SYSTEM OF IRIDIUM MONOFLUORIDE, IrF.

XIUJUAN ZHUANG AND TIMOTHY C. STEIMLE, Department of Chemistry and Biochemistry, Arizona State University, Tempe,AZ 85287; COLAN LINTON, Center for Lasers, Atomic and Molecular Sciences and Physics Department, University of New Brunswick, Fredericton, NB Canada E3B 5A3.

Recently the New Brunswick group reported on the field-free detection and analysis of the A3 Phi4-X3 Phi4 band system of IrF. Here we report on the analysis Q(4)(15922 cm-1) branch feature of the (1,0) band of the 191IrF isotopologue of that system recorded at field strengths of up to 3000 V/cm. The spectra are surprisingly complex at the achieved resolution of 40 MHz due to the presence of both the 191Ir(I=3/2) and 19F(I=1/2) magnetic hyperfine splitting. The determined permanent electric dipole moment, µel, for the X3 Phi4 state is compared with that recently determined for the X3 Phi4 state of isovalent CoF. The trend in µel amongst the ground states of IrF, IrC and IrN will be discussed. Finally, a simple molecular orbital correlation diagram will be used to rationalize the change in µel upon excitation from the X3 Phi4 to A3 Phi4 state.