| Literature DB >> 29939444 |
Alexey S Berezin1, Katerina A Vinogradova1,2, Viktor P Krivopalov3, Elena B Nikolaenkova3, Victor F Plyusnin2,4, Arkady S Kupryakov2,4, Natalia V Pervukhina1,2, Dmitrii Y Naumov1,2, Mark B Bushuev1,2.
Abstract
Manipulating the relaxation pathways of excited states and understanding mechanisms of photochemical reactions present important challenges in chemistry. Here we report a unique zinc(II) complex exhibiting unprecedented interplay between the excitation-wavelength-dependent emission, thermally activated delayed fluorescence (TADF) and excited state intramolecular proton transfer (ESIPT). The ESIPT process in the complex is favoured by a short intramolecular OH⋅⋅⋅N hydrogen bond. Synergy between the excitation-wavelength-dependent emission and ESIPT arises due to heavy zinc atom favouring intersystem crossing (isc). Reverse intersystem crossing (risc) and TADF are favoured by a narrow singlet-triplet gap, ΔEST ≈10 kJ mol-1 . These results provide the first insight into how a proton-transfer system can be modified to show a synergy between the excitation-wavelength-dependent emission, ESIPT and TADF. This strategy offers new perspectives for designing ESIPT and TADF emitters exhibiting tunable excitation-wavelength-dependent luminescence.Entities:
Keywords: delayed fluorescence; fluorescence; kinetics; photochemistry; proton transfer
Year: 2018 PMID: 29939444 DOI: 10.1002/chem.201802876
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236