Intermolecular hydrogen-bonding effects on photophysics and photochemistry

• Published in: International reviews in physical chemistry Vol. 32; no. 4; pp. 589 - 609
• Main Authors: Song, Peng, Ma, Feng-Cai
• Format: Journal Article
• Language: English
• Published: Abingdon Routledge 01.12.2013; Taylor & Francis Ltd
• Subjects: Chemical reactions; dihydrogen bond; Dynamics; Excitation; Excitation spectra; excited-state double proton transfer; fluorescence quenching; fluorescent probes; Geometry; Hydrogen bonding; Hydrogen bonds; intermolecular hydrogen bonding; Molecular physics; Photochemistry; photophysics and photochemistry; Protons; sensing mechanism; Spectra; spectral shifts; Spectrum analysis; Strengthening
• ISSN: 0144-235X; 1366-591X
• DOI: 10.1080/0144235X.2013.811891

Intermolecular hydrogen bonding, as an important site-specific interaction between hydrogen donor and acceptor molecules both in the gas phase and in solution, plays a significant role and has a remarkable influence on the photophysics and photochemistry of chromophores in the hydrogen-bonding surroundings. In recent years, the excited-state structures and dynamics of the intermolecular hydrogen bonding have been widely investigated by using both the experimental and theoretical methods. This review article focuses on the recent research progress of the important intermolecular hydrogen-bonding effects on the non-adiabatic photophysical processes and photochemical reactions. Firstly, the corresponding relationship between electronic spectral red-shift or blue-shift and excited-state intermolecular hydrogen bond strengthening or weakening has been clarified. A dynamic equilibrium induced by the intermolecular hydrogen bond strengthening in the electronically excited state of fluorenone chromophore was used to explain the steady-state spectral features. The stepwise mechanism of excited-state double proton transfer reaction for the 2-aminopyridine/acid systems was demonstrated. The role of intermolecular hydrogen bonding on the excited-state proton transfer in the sensing mechanism of fluorescent probes has also been discussed. Moreover, a dihydrogen-bonded complex formed by borane-trimethylamine and phenol showed interesting geometric structures and infared spectrum in electronically excited state.