Time-resolved observations have been made of the formation of vibrationally excited NO X Π (') following collisional quenching of NO A Σ ( = 0) by NO X Π ( = 0). Two time scales are observed, namely a fast production rate consistent with direct formation from the quenching of the electronically excited NO A state, together with a slow component, the magnitude and rate of formation of which depend upon NO pressure. A reservoir state formed by quenching of NO A Σ ( = 0) is invoked to explain the observations, and the available evidence points to this state being the first electronically excited state of NO, a Π. The rate constant for quenching of the a Π state to levels ' = 11-16 by NO is measured as (8.80 ± 1.1) × 10 cm molecule s at 298 K where the error quoted is two standard deviations, and from measurements of the increased formation of high vibrational levels of NO(X) by the slow process we estimate a lower limit for the fraction of self-quenching collisions of NO A Σ ( = 0) which lead to NO a Π as 19%.
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J Fluoresc
January 2025
Department of Chemistry, The University of Burdwan, Golapbag, Burdwan, 713104, India.
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Department of Psychology, Chinese University of Hong Kong, Hong Kong SAR, China
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January 2025
Department of Molecular and Cell Biology and School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA. Electronic address:
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