Planarized intramolecular charge transfer: a concept for fluorophores with both large stokes shifts and high fluorescence quantum yields

Abstract Fluorophores were successfully used in several areas of chemistry and biochemistry. For many purposes, however, it is necessary that the fluorescence compound features a high fluorescence quantum yield as well as a large Stokes shift. The latter is, for example, achieved by the use of a twi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Haberhauer, Gebhard (VerfasserIn) , Gleiter, Rolf (VerfasserIn) , Burkhart, Christoph (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 08 January 2016
In: Chemistry - a European journal
Year: 2016, Jahrgang: 22, Heft: 3, Pages: 971-978
ISSN:1521-3765
DOI:10.1002/chem.201503927
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/chem.201503927
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201503927
Volltext
Verfasserangaben:Gebhard Haberhauer, Rolf Gleiter, and Christoph Burkhart
Beschreibung
Zusammenfassung:Abstract Fluorophores were successfully used in several areas of chemistry and biochemistry. For many purposes, however, it is necessary that the fluorescence compound features a high fluorescence quantum yield as well as a large Stokes shift. The latter is, for example, achieved by the use of a twisted intramolecular charge-transfer (TICT) compound, which shows a twisted geometry in the excited state. However, the higher the twisting is, the lower becomes in general the fluorescence quantum yield as the resulting emission from the twisted state is forbidden. In order to escape this dilemma, we propose the model of planarized intramolecular charge-transfer (PLICT) states. These compounds are completely twisted in the ground states and planar in the excited states. By means of quantum chemical calculations (time-dependent (TD)-B3LYP and CC2) and experimental studies, we could demonstrate that 1-aminoindole and its derivatives form photoinduced PLICT states. They show both very large Stokes shifts ( =9000?13?500?cm?1, i.e., ?=100?150?nm) and high fluorescence quantum yields. These characteristics and their easy availability starting from the corresponding indoles, make them very attractive for the use as optical switches in various fields of chemistry as well as biological probes.
Beschreibung:Gesehen am 02.09.2020
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201503927