Dual emissive bodipy–benzodithiophene–bodipy TICT triad with a remarkable Stokes shift of 194 nm

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DC Field	Value	Language
dc.contributor.author	Sengupta, S.	-
dc.contributor.author	Pandey, U.K.	-
dc.date.accessioned	2020-11-26T06:50:05Z	-
dc.date.available	2020-11-26T06:50:05Z	-
dc.date.issued	2018	-
dc.identifier.citation	Organic and Biomolecular Chemistry, 16(12), pp. 2033-2038	en_US
dc.identifier.other	https://doi.org/10.1039/C8OB00272J	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00272j#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/2262	-
dc.description.abstract	An acceptor–donor–acceptor (A–D–A) triad based on a BODIPY acceptor and a benzodithiophene donor exhibited dual fluorescence and pronounced fluorescence solvatochromism because of twisted intramolecular charge transfer (TICT) state formation. Furthermore, it showed a Stokes shift of ∼194 nm which is the highest known for any BODIPY compound with a readily tunable fluorescence and a high charge carrier mobility of 4.46 × 10−4 cm2 V−1 s−1.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Dipyrromethene	en_US
dc.subject	Benzodithiophene	en_US
dc.subject	Bodipy	en_US
dc.subject	Singlet Oxygen	en_US
dc.title	Dual emissive bodipy–benzodithiophene–bodipy TICT triad with a remarkable Stokes shift of 194 nm	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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