Jin Bing, Sheridan Phillip M, Clouthier Dennis J
Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.
Department of Chemistry and Biochemistry, Canisius College, Buffalo, New York 14208, USA.
J Chem Phys. 2015 Mar 28;142(12):124301. doi: 10.1063/1.4915126.
In this and previous work [D. J. Clouthier, J. Chem. Phys. 141, 244309 (2014)], the spectroscopic signatures of the X2BY (X = H, halogen, Y = O, S) free radicals have been predicted using high level ab initio theory. The theoretical results have been used to calculate the electronic absorption and single vibronic level (SVL) emission spectra of the radicals under typical jet-cooled conditions. Using these diagnostic predictions, the previously unknown F2BS and Cl2BS free radicals have been identified and characterized. The radicals were prepared in a free jet expansion by subjecting precursor mixtures of BF3 or BCl3 and CS2 vapor to an electric discharge at the exit of a pulsed molecular beam valve. The B̃(2)A1-X̃(2)B2 laser-induced fluorescence spectra were found within 150 cm(-1) of their theoretically predicted positions with vibronic structure consistent with our Franck-Condon simulations. The B̃(2)A1 state emits down to the ground state and to the low-lying Ã(2)B1 excited state and the correspondence between the observed and theoretically derived SVL emission Franck-Condon profiles was used to positively identify the radicals and make assignments. Excited state Coriolis coupling effects complicate the emission spectra of both radicals. In addition, a forbidden component of the electronically allowed B̃-X̃ band system of Cl2BS is evident, as signaled by the activity in the b2 modes in the spectrum. Symmetry arguments indicate that this component gains intensity due to a vibronic interaction of the B̃(2)A1 state with a nearby electronic state of (2)B2 symmetry.
