Vibrations of porphycene in the S and S1 electronic states: Single vibronic level dispersed fluorescence study in a supersonic jet

• Published in: The Journal of chemical physics 2013-05, Vol.138 (17)
• Main Authors: Mengesha, Ephriem T., Sepioł, Jerzy, Borowicz, Paweł, Waluk, Jacek
• Format: Article
• Language: English
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.4802769

Supersonic jet-isolated porphycene has been studied using the techniques of laser-induced fluorescence excitation, single vibronic level fluorescence, and spectral hole burning, combined with quantum mechanical calculations of geometry and vibrational structure of the ground and lowest electronically excited singlet states. Porphycene is a model for coherent double hydrogen tunneling in a symmetrical double well potential, as evidenced by tunneling splittings observed in electronic absorption and emission. The results led to reliable assignment of low frequency modes in S0 and S1 electronic states. The values of tunneling splitting were determined for ground state vibrational levels. In the case of tautomerization-promoting 2Ag mode, tunneling splitting values significantly increase with the vibrational quantum number. Mode coupling was demonstrated by different values of tunneling splitting obtained for coexcitation of two or more vibrations. Finally, alternation of relative intensity patterns for the components of 2Ag tunneling doublet observed for excitation and emission into different vibrational levels suggests that the energy order of levels corresponding to (+) and (−) combinations of nuclear wave functions is different for even and odd vibrational quantum numbers.