期刊
MOLECULES
卷 27, 期 19, 页码 -出版社
MDPI
DOI: 10.3390/molecules27196245
关键词
methylpyrazine; photoelectron imaging; intersystem crossing; pump-probe; time-resolved spectroscopy
资金
- Xinjiang Autonomous Region Outstanding Youth Fund Project [2022D01E12]
- National Natural Science Foundation of China [21763027]
- Innovation Team for Monitoring of Emerging Contaminants and Biomarkers [2021D14017]
- Xinjiang Graduate Education and Teaching Reform Project [XJ2021GY25]
- Xinjiang Regional Collaborative Innovation Project [2019E0223]
- Undergraduate Teaching Research and Reform Project of Xinjiang Normal University [SDJG2021-12]
- Scientific Research Program of Colleges and Universities in Xinjiang [XJEDU2020Y029]
- 13th Five-Year Plan for the Key Discipline Physics Bidding Project of Xinjiang Normal University [17SDKD0602]
This study investigates the excited state dynamics of 2-methylpyrazine and observes its decay pathways via intersystem crossing and internal conversion.
2-methylpyrazine was excited to the high vibrational dynamics of the S-1 state with 260 nm femtosecond laser light, and the evolution of the excited state was probed with 400 nm light. Because it was unstable, the S-1 state decayed via intersystem crossing to the triplet state T-1, and it may have decayed to the ground state S-0 via internal conversion. S-1-to-T-1 intersystem crossing was observed by combining time-resolved mass spectrometry and time-resolved photoelectron spectroscopy. The crossover time scale was 23 ps. Rydberg states were identified, and the photoelectron spectral and angular distributions indicated accidental resonances of the S-1 and T-1 states with the 3s and 3p Rydberg states, respectively, during ionization.
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