Literature DB >> 22193300

Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials.

Jianzhang Zhao1, Shaomin Ji, Yinghui Chen, Huimin Guo, Pei Yang.   

Abstract

In this perspective we introduce the basic photophysics of the excited-state intramolecular proton transfer (ESIPT) chromophores, then the state-of-the-art development of the ESIPT chromophores and their applications in chemosensors, biological imaging and white-light emitting materials are summarized. Most of the applications of the ESIPT chromophores are based on the photophysics properties, such as design of fluorescent chemosensors by perturbation of the ESIPT process upon interaction with the analytes, their use as biological fluorescent tags to study DNA-protein interaction by probing the variation of the hydration, or design of white-light emitting materials by employing the large Stokes shift of the ESIPT chromophores (to inhibit the Föster energy transfer of the components). The photophysical mechanism of these applications is discussed. Furthermore, a new research topic concerning the ESIPT chromophores is proposed based on our group's results, that is, to develop organic triplet sensitizers with ESIPT chromophores.

Year:  2011        PMID: 22193300     DOI: 10.1039/c2cp23144a

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  69 in total

Review 1.  Artificial Molecular Machines.

Authors:  Sundus Erbas-Cakmak; David A Leigh; Charlie T McTernan; Alina L Nussbaumer
Journal:  Chem Rev       Date:  2015-09-08       Impact factor: 60.622

2.  Substituent control of photophysical properties for excited-state intramolecular proton transfer (ESIPT) of o-LHBDI derivatives: a TD-DFT investigation.

Authors:  Mei Ni; Shenyang Su; Hua Fang
Journal:  J Mol Model       Date:  2020-04-23       Impact factor: 1.810

3.  Theoretical investigations on forward-backward ESIPT processes of three fluorophores deriving from 2-(2'-hydroxyphenyl)thiazole.

Authors:  Xiuning Liang; Hua Fang
Journal:  Photochem Photobiol Sci       Date:  2021-03-31       Impact factor: 3.982

4.  Large fluorescence response by alcohol from a bis(benzoxazole)-zinc(II) complex: the role of excited state intramolecular proton transfer.

Authors:  Junfeng Wang; Qinghui Chu; Xiumin Liu; Chrys Wesdemiotis; Yi Pang
Journal:  J Phys Chem B       Date:  2013-04-03       Impact factor: 2.991

5.  A combined experimental and DFT-TDDFT study of the excited-state intramolecular proton transfer (ESIPT) of 2-(2'-hydroxyphenyl) imidazole derivatives.

Authors:  Vikas S Padalkar; Ponnadurai Ramasami; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2013-04-24       Impact factor: 2.217

6.  Visible-to-NIR-Light Activated Release: From Small Molecules to Nanomaterials.

Authors:  Roy Weinstain; Tomáš Slanina; Dnyaneshwar Kand; Petr Klán
Journal:  Chem Rev       Date:  2020-10-30       Impact factor: 60.622

7.  The Effect of Substituent Position on Excited State Intramolecular Proton Transfer in Benzoxazinone Derivatives: Experiment and DFT Calculation.

Authors:  Gao-Feng Bian; Yun Guo; Xiao-Jing Lv; Cheng Zhang
Journal:  J Fluoresc       Date:  2016-10-18       Impact factor: 2.217

8.  Detection of boronic acids through excited-state intramolecular proton-transfer fluorescence.

Authors:  Matthew R Aronoff; Brett VanVeller; Ronald T Raines
Journal:  Org Lett       Date:  2013-10-07       Impact factor: 6.005

9.  Comprehensive DFT and TD-DFT Studies on the Photophysical Properties of 5,6-Dichloro-1,3-Bis(2-Pyridylimino)-4,7-Dihydroxyisoindole: A New Class of ESIPT Fluorophore.

Authors:  Santosh Kataria; Lydia Rhyman; Ponnadurai Ramasami; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2016-07-25       Impact factor: 2.217

10.  TDDFT calculations of electronic spectra of benzoxazoles undergoing excited state proton transfer.

Authors:  Y Syetov
Journal:  J Fluoresc       Date:  2013-03-09       Impact factor: 2.217

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