Journal
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
Volume 250, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2020.119394
Keywords
Excited state intramolecular proton transfer; Charge reorganization; Solvent polarity; Intramolecular hydrogen bond; Frontier molecular orbital
Categories
Funding
- National Natural Science Foundation of China [21873114]
- China Postdoctoral Science Foundation [2020M682154]
- state key laboratory of molecular reaction dynamics in DICP, CAS
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This study investigates the photo-induced excited state hydrogen bonding interactions and excited state proton transfer behaviors of HPBB compound in solvents with different polarities. The enhanced excited state hydrogen bonds of HPBB are more prominent in nonpolar solvents. Analysis of hydrogen bond geometrical parameters and charge redistribution reveals the influence of solvent polarity on the ESIDPT mechanism.
In this work, we probe into the photo-induced excited state hydrogen bonding interactions and excited state proton transfer (ESPT) behaviors for a representative benzo[1,2-d:4,5-d']bisimidazole derivative (i.e., 2-hydroxyphenyl-substituted benzo[1,2-d:4,5-d']bisimidazole (HPBB)) compound. In view of aprotic solvents with different polarities, cyclohexane (CYH), dichloromethane (DCM) and acetonitrile (MeCN) solvents are considered. Analyzing hydrogen-bond geometrical parameters, infrared (IR) vibrational spectra, Mayer bond order and predicting hydrogen bonding energy (E-(HB)), we verify dual hydrogen bonds of HPBB are strengthened in S-1 state. Particularly, in nonpolar solvent, the enhanced excited state hydrogen bonds become more obvious. The intriguing charge redistribution and frontier molecular orbitals (MOs) reveal hydrogen bonding acceptance ability of acceptor moieties becomes stronger, which plays a crucial role in capturing hydroxyl proton via photoexcitation. To check and explore ESIPT mechanism, we present the solvent polarity dependent asynchronous excited state intramolecular double proton transfer (ESIDPT) mechanism. That is, nonpolar solvent promotes excited state intramolecular single proton transfer (ESISPT) process for HPBB, while polar solvent contributes to ESIDPT behavior with the primary single proton-transfer product in S-1 state. This work not only makes a rational attribution to experimental phenomena, but also clarifies detailed excited state behaviors for HPBB and presents regulating ESIPT mechanism via solvent polarity. (C) 2020 Elsevier B.V. All rights reserved.
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