Abstract
The H atom tunneling dissociation dynamics of the S1 state of meta- or para-cresol has been investigated by using the picosecond time-resolved pump-probe spectroscopy in a state-specific manner. The S1 state lifetime (mainly due to the H atom tunneling reaction) is found to be mode-dependent whereas it quickly converges and remains constant as the rapid intramolecular vibrational energy redistribution (IVR) starts to participate in the S1 state relaxation with the increase of the S1 internal energy (Eint). The IVR rate and its change with increasing Eint have been reflected in the parent ion transients taken by tuning the total energy (hνpump + hνprobe) just above the adiabatic ionization threshold (so that the dissipation of the initial mode-character could be monitored as a function of the reaction time), indicating that the mode randomization rate into the S1 isoenergetic manifolds exceeds the tunneling rate quite early in terms of Eint for m-cresol (≤∼1200cm-1) or p-cresol (≤∼800cm-1) compared to the case of phenol (≤∼1800cm-1). Though the H atom tunneling dynamics of phenol (S1) seems to be little influenced by the methyl substitution on the either m- or p-position, the IVR rate has been found to be strongly accelerated due to the sharply-increasing (S1) density of states with increasing Eint due to the pivotal role of the low-frequency CH3 torsional mode.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
