Literature DB >> 21142199

Switchable three-state fluorescence of a nonconjugated donor-acceptor triarylborane.

Zachary M Hudson1, Xiang-Yang Liu, Suning Wang.   

Abstract

A nonconjugated fluorescent molecule with a triarylboron acceptor and an alkylamine donor has been found to display bright green fluorescence due to charge transfer through space, which can be reversibly deactivated by blocking either the donor or acceptor site. Binding of the fluoride ion to boron switches the fluorescence color to sky blue, while protonation of the amine with acid switches the emission color to the purple fluorescence of the acceptor chromophore.

Entities:  

Year:  2010        PMID: 21142199     DOI: 10.1021/ol102749y

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Dual-Emissive Difluoroboron Naphthyl-Phenyl β-Diketonate Polylactide Materials: Effects of Heavy Atom Placement and Polymer Molecular Weight.

Authors:  Jelena Samonina-Kosicka; Christopher A DeRosa; William A Morris; Ziyi Fan; Cassandra L Fraser
Journal:  Macromolecules       Date:  2014-05-23       Impact factor: 5.985

2.  Arylisoquinoline-derived organoboron dyes with a triaryl skeleton show dual fluorescence.

Authors:  Vânia F Pais; Tristan Neumann; Ignacio Vayá; M Consuelo Jiménez; Abel Ros; Uwe Pischel
Journal:  Beilstein J Org Chem       Date:  2019-11-04       Impact factor: 2.883

3.  Fluoride binding to an organoboron wire controls photoinduced electron transfer.

Authors:  Jing Chen; Oliver S Wenger
Journal:  Chem Sci       Date:  2015-05-01       Impact factor: 9.825

  3 in total

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