INFRAFRED OPTICAL DOUBLE RESONANCE SPECTROSCOPY OF THE $NH-2$ RADICAL

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1980

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Ohio State University

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Vibration-rotation transition of NH2 in the A~2A1 state were observed with sub-Doppler resolution by using a dye laser and a CO2/N2O laser combined with the laser magnetic resonance technique. The cw dye laser output (Rh 6G, 70 mW) was introduced into a fluorescence cell placed in the CO2/N2O laser cavity through a ZnSe partial reflector. The infrared laser was modulated by an intracavity chopper, and the double resonance signal was observed as a change in fluorescence intensity by using a phase-sensitive detector. When the dye laser pumped the A~2A1(090)22 0X~2B1(000)11 0 transition 29MJ components of (0100)211−(090)22 0 in {\AA} were observed by sweeping the magnetic field. An analysis of the observed spectra revealed a large change in the orbital magnetic g-factor along the a-axis, gaa, between the v2=9 and 10 vibrational state: -0.1246 (39) and -0. 0506(55) in (090) and (0 10 0), respectively. Three additional lines which corresponded to changes in fluorescence intensity opposite in sign to those for the 29 M components mentioned above, were also observed and tentatively assigned to transition from A~2A1 (090) to a highly excited vibrational state of X~.

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