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Triarylborane-Appended New Triad and Tetrad: Chromogenic and Fluorogenic Anion Recognition

Swamy, Chinna Ayya P and Thilagar, Pakkirisamy (2014) Triarylborane-Appended New Triad and Tetrad: Chromogenic and Fluorogenic Anion Recognition. In: INORGANIC CHEMISTRY, 53 (6). pp. 2776-2786.

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Official URL: http://dx.doi.org/10.1021/ic402898n


Facile synthesis of triad 3 and tetrad 4 incorporating -B(Mes)(2) (Mes = mesityl (2,4,6-trimethylphenyl)), boron dipyrromethene (BODIPY), and triphenylamine is reported. Introduction of two dissimilar acceptors (triarylborane and BODIPY) on a single donor resulted in two distinct intramolecular charge transfer processes (amine-to-borane and amine-to-BODIPY). The absorption and emission properties of the new triad and tetrad are highly dependent on individual building units. The nature of electronic communication among the individual fluorophore units has been comprehensively investigated and compared with building units. Compounds 3 and 4 showed chromogenic and fluorogenic responses for small anions such as fluoride and cyanide.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to the AMER CHEMICAL SOC, USA
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 22 May 2014 06:20
Last Modified: 22 May 2014 06:20
URI: http://eprints.iisc.ac.in/id/eprint/48978

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