Journal of Chemical Physics, Vol.120, No.6, 2662-2666, 2004
Laser-induced fluorescence spectroscopy of NC3S
In a discharged supersonic jet of acetonitrile and carbon disulfide, we have for the first time observed an electronic transition of the NC3S radical using laser-induced fluorescence (LIF) spectroscopy. A progression originating from the C-S stretching mode of the upper electronic state appears in the excitation spectrum. Each band of the progression has a polyad structure due to anharmonic resonances with even overtones of bending modes. Rotationally resolved spectra have been observed by high-resolution laser scans, and the electronic transition is assigned to (A) over tilde (2)Pi(i)-(X) over tilde (2)Pi(i). For the vibronic origin band, the position and the effective rotational constant of the upper level have been determined to be 21 553.874(1) and 0.046 689(4) cm(-1), respectively. The dispersed fluorescence spectrum from the zero vibrational level of (A) over tilde (2)Pi(3/2) has also been observed; its vibrational structure is similar to that of the LIF excitation spectrum, showing a prominent C-S stretching progression with polyad structures. The vibrational frequencies of the C-S stretching mode in the ground and excited electronic states are determined to be 550 and 520 cm(-1), respectively. Fluorescence decay profiles have been measured for several vibronic levels of the A state. (C) 2004 American Institute of Physics.