Intersystem Crossing of 2-Methlypyrazine Studied by Femtosecond Photoelectron Imaging

Molecules. 2022 Sep 22;27(19):6245. doi: 10.3390/molecules27196245.

Abstract

2-methylpyrazine was excited to the high vibrational dynamics of the S1 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 S1 state decayed via intersystem crossing to the triplet state T1, and it may have decayed to the ground state S0 via internal conversion. S1-to-T1 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 S1 and T1 states with the 3s and 3p Rydberg states, respectively, during ionization.

Keywords: intersystem crossing; methylpyrazine; photoelectron imaging; pump–probe; time-resolved spectroscopy.

MeSH terms

  • Diagnostic Imaging
  • Lasers
  • Photoelectron Spectroscopy
  • Quantum Theory*
  • Vibration*

Grants and funding

This work was supported by the Xinjiang Autonomous Region Outstanding Youth Fund Project (2022D01E12), the National Natural Science Foundation of China (No. 21763027), the Innovation Team for Monitoring of Emerging Contaminants and Biomarkers (2021D14017), the Xinjiang Graduate Education and Teaching Reform Project (No. XJ2021GY25), the Xinjiang Regional Collaborative Innovation Project (No. 2019E0223), the Undergraduate Teaching Research and Reform Project of Xinjiang Normal University (No. SDJG2021-12), the Scientific Research Program of Colleges and Universities in Xinjiang (No. XJEDU2020Y029), and the “13th Five-Year” Plan for the Key Discipline Physics Bidding Project of Xinjiang Normal University (No. 17SDKD0602). All of the above funding programs are thanked for their support.