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• W2000699497 abstract "A broad and relatively unstructured electronic excitation spectrum has been observed for the OH–CO reactant complex in the OH A–X (1,0) region by laser-induced fluorescence and fluorescence depletion methods. The electronic spectrum spans from 33 500 to 36050cm−1 and peaks near 34600cm−1. Fluorescence depletion methods have been employed to demonstrate that the broad electronic spectrum originates from the same linear, hydrogen-bonded OH–CO complex that gives rise to a rotationally resolved infrared spectrum. The electronic spectrum is consistent with a Franck–Condon mapping of the ground state radial distribution on a strongly attractive excited state potential that undergoes rapid decay dynamics." @default.
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• W2000699497 date "2002-03-01" @default.
• W2000699497 modified "2023-10-18" @default.
• W2000699497 title "Electronic spectroscopy of the OH–CO reactant complex" @default.
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• W2000699497 doi "https://doi.org/10.1016/s0009-2614(02)00061-1" @default.
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