Relaxation dynamics of NH stretching vibrations of 2-aminopyridine and its dimer in a supersonic beam

Yamada Yuji

Mikami Naohiko

Ebata Takayuki

Proceedings of the National Academy of Sciences of the United States of America

Picosecond time-resolved IR-UV pump-probe spectroscopy has been carried out in order to elucidate vibrational energy relaxation (VER) of the NH stretching vibrations of 2-aminopyridine monomer (2AP) and dimer ((2AP)2) in supersonic beams. In bare 2AP, intramolecular vibrational energy redistribution (IVR) of the NH vibrations is described by the two bath mode model, where the initial vibrational energy flows to the doorway states rapidly (6.5 ps) and then dissipates into the dense bath states with a time constant of ~20 ps. No clear difference was observed in the IVR lifetime between the symmetric and asymmetric NH2 stretch modes. In (2AP)2, IVR and vibrational predissociation (VP) were involved in VER. It was found that the rate constants of both IVR and VP of the hydrogen-bonded NH stretching vibration are larger than those of the free NH.

Chemistry [ 430 ]

eng

National Academy of Sciences

Copyright (c) 2008 by The National Academy of Sciences of the USA

[ISSN] 0027-8424

[DOI] 10.1073/pnas.0800354105

[NCID] AA10808769

[DOI] http://dx.doi.org/10.1073/pnas.0800354105