Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process

Recently, organic fluorescent molecules harnessing the excited‐state intramolecular proton transfer (ESIPT) process are drawing great attention due to their unique photophysical properties which facilitate novel optoelectronic applications. After a brief introduction to the ESIPT process and related...

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Bibliographic Details
Published inAdvanced materials (Weinheim) Vol. 23; no. 32; pp. 3615 - 3642
Main Authors Kwon, Ji Eon, Park, Soo Young
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 23.08.2011
WILEY‐VCH Verlag
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Summary:Recently, organic fluorescent molecules harnessing the excited‐state intramolecular proton transfer (ESIPT) process are drawing great attention due to their unique photophysical properties which facilitate novel optoelectronic applications. After a brief introduction to the ESIPT process and related photo­physical properties, molecular design strategies towards tailored emission are discussed in relation to their theoretical aspects. Subsequently, recent studies on advanced ESIPT molecules and their optoelectronic applications are surveyed, particularly focusing on chemical sensors, fluorescence imaging, proton transfer lasers, and organic light‐emitting diodes (OLEDs). Organic fluorescent molecules harnessing excited‐state intramolecular proton transfer (ESIPT) process are drawing great attention due to their unique and beneficial photophysical properties such as a large Stokes' shift, no self‐absorption, and easy population inversion of the keto form, which are attributed to its intrinsic four‐level photocycle scheme. Here, recent studies on advanced ESIPT molecules and their novel optoelectronic applications are reviewed.
Bibliography:istex:B4D233E4921FA5E66CF0409637173954FC96D71D
ark:/67375/WNG-LK5VF573-W
ArticleID:ADMA201102046
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0935-9648
1521-4095
1521-4095
DOI:10.1002/adma.201102046