New insights into the solvent-assisted excited-state double proton transfer of 2-(1H-pyrazol-5-yl)pyridine with alcoholic partners: A TDDFT investigation

作者：Li Hui; Shi Ying^*; Yin Hang; Wang Ye; Cong Lin; Jin Mingxing; Ding Dajun

来源：Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy , 2015, 141: 211-215.

DOI：10.1016/j.saa.2015.01.060

• Excited-state double proton transfer (ESDPT)
• TDDFT
• Hydrogen bond
• Infrared (IR) spectrum

Excited-state double proton transfer (ESDPT) in the hydrogen-bonded 2-(1H-pyrazol-5-yl)pyridine with propyl alcoholic partner (PPP) was theoretically investigated by time-dependent density functional theory (TDDFF) method. Great changes have taken place for the calculated geometric structures, the electron density features and vibrational spectrum of PPP system in So and S-1 state. Our results have demonstrated that ESDPT reaction happens within the system upon photoexcitation. We also found that the ESDPT process is facilitated by the electronically excited state intermolecular hydrogen bond strengthening. Particularly, after the photoexcitation from HOMO(pi) to the LUMO(pi*), the rearrangement of electronic density distribution of frontier molecular orbitals CMOs) on pyridine and the pyrazol moieties exhibits a very important positive factor for the ESDPT. Furthermore, by the investigation of the stretching vibrations of N-H and O-H groups, the infrared (IR) spectroscopic results provide us not only a theoretical evidence of ESDPT, but also a considerable clue to characterize the nature of intermolecular reaction. In addition, efforts have also been devoted towards calculating the absorption peak, which shows good consistency with the experimental result of the studied system.

• 出版日期2015-4-15
• 单位吉林大学