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