Excited state non-adiabatic dynamics of N-methylpyrrole: A time-resolved photoelectron spectroscopy and quantum dynamics study

Guorong Wu, Simon P Neville, Oliver Schalk, Taro Sekikawa, Michael N R Ashfold, Graham A Worth, Albert Stolow

Research output: Contribution to journalArticle (Academic Journal)peer-review

18 Citations (Scopus)
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Abstract

The dynamics of N-methylpyrrole following excitation at wavelengths in the range 241.5-217.0 nm were studied using a combination of time-resolved photoelectron spectroscopy (TRPES), ab initio quantum dynamics calculations using the multi-layer multi-configurational time-dependent Hartree method, as well as high-level photoionization cross section calculations. Excitation at 241.5 and 236.2 nm results in population of the A2(πσ(∗)) state, in agreement with previous studies. Excitation at 217.0 nm prepares the previously neglected B1(π3py) Rydberg state, followed by prompt internal conversion to the A2(πσ(∗)) state. In contrast with the photoinduced dynamics of pyrrole, the lifetime of the wavepacket in the A2(πσ(∗)) state was found to vary with excitation wavelength, decreasing by one order of magnitude upon tuning from 241.5 nm to 236.2 nm and by more than three orders of magnitude when excited at 217.0 nm. The order of magnitude difference in lifetimes measured at the longer excitation wavelengths is attributed to vibrational excitation in the A2(πσ(∗)) state, facilitating wavepacket motion around the potential barrier in the N-CH3 dissociation coordinate.

Original languageEnglish
Article number014309
Number of pages12
JournalJournal of Chemical Physics
Volume144
Issue number1
Early online date7 Jan 2016
DOIs
Publication statusPublished - Jan 2016

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