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 4-X3 4 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 4 state is compared with that recently determined for the X3 4 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 4 to A3 4 state.