Experimental and theoretical insights into the influence of electronic density on proton-transfer reactions. Issue 42 (18th October 2018)

• Record Type: Journal Article
• Authors: Gomez, Eduardo; Alarcos, Noemí; Monterde, Cristina; Sánchez, Félix; Moreno, Miquel; Douhal, Abderrazzak
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 42(2018)
• Page Start: 27149
• Page End: 27161
• Publication Date: 2018-10-18
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp03185a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Time-resolved and theoretical studies elucidating the origin of abnormally slow proton-motion dynamics in solutions. Abstract : We report on the excited-state behavior of proton-transfer phenanthroimidazole derivatives, such as HPPI and NMHPPI, in solutions using steady-state and femto- to nanosecond time-resolved fluorescence spectroscopies. Experimental observations are supported by theoretical calculations (TDDFT). In dichloromethane (DCM) and acetonitrile (ACN), two different paths are found for the excited-state intramolecular proton-transfer (ESIPT) reactions following two different channels. A fast and direct channel (ESIPT1 ) in 1–2.5 ps and a slower one (ESIPT2 ) in 12–15 ps, the latter being more influenced by the solvent viscosity (30 ps for HPPI and 20 ps for NMHPPI in triacetin (TAC) solutions). The slowing down of the ESIPT2 reaction is explained in terms of an intramolecular charge transfer (ICT) reaction coupled to a twisting motion to reach a more suitable conformation of the involved parts in the proton-transfer motion. The absence of OH/OD exchange effects in the ultrafast and slow proton-transfer dynamics suggests that the ESIPT reactions, which involve intramolecular and solvent coordinates, do not occur via tunneling. These results reveal new insights into the photobehavior of proton-transfer dyes, which might help in designing photosensors or lighting devices.