Effect of the substitution position (2, 3 or 8) on the spectroscopic and photophysical properties of BODIPY dyes with a phenyl, styryl or phenylethynyl group

Orte, Angel and Debroye, Elke and Ruedas-Rama, Maria J. and Garcia-Fernandez, Emilio and Robinson, David and Crovetto, Luis and Talavera, Eva M. and Alvarez-Pez, Jose M. and Leen, Volker and Verbelen, Bram and Dias de Rezende, Lucas Cunha and Dehaen, Wim and Hofkens, Johan and Van der Auweraer, Mark and Boens, Noël (2016) Effect of the substitution position (2, 3 or 8) on the spectroscopic and photophysical properties of BODIPY dyes with a phenyl, styryl or phenylethynyl group. RSC Advances, 6 . pp. 102899-102913. ISSN 2046-2069

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Abstract

A very active branch of organic chemistry is putting great effort in tailoring fluorescent dyes for a myriad of applications, from technological to bioanalytical and biomedical applications. Among the major families of fluorophores, those derived from 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY dyes) are undergoing a recent boost thanks to the simplicity and robustness of the chemistry involved. The BODIPY core can be modified with numerous side groups, the 8-position being a modification place with important effects on the spectroscopic and photophysical properties of the resulting dyes. Likewise, previous work has shown that the addition of groups attached at the 3- and 2-positions can result in dyes with very different properties. Herein, we generalize the effect of the substituent side groups by studying nine BODIPY dyes substituted with a phenyl, styryl or phenylethynyl moiety at the 2-, 3- or 8-position of the BODIPY scaffold. Within the class of phenyl- or phenylethynyl-substituted dyes, substitution at the 2-position always leads to dyes with the broadest bandwidths and the largest Stokes shifts. We investigate the solvent effect on the spectroscopic properties of the dyes, using four empirical solvent scales (dipolarity, polarizability, acidity and basicity: Catalán, J. Phys. Chem., 2009, 113, 5951). These analyses identify solvent dipolarity and polarizability as critical parameters accounting for the observed solvent-dependent shifts of the absorption and emission maxima. Finally, time-dependent density functional theory calculations provide insights into the structural and energetic issues concerning the spectroscopic properties of these fluorophores.

Item Type: Article
Keywords: Fluorescent dyes, solvent effect, Catalán solvent scales, quantum chemical calculations
Schools/Departments: University of Nottingham, UK > Faculty of Science > School of Chemistry
Identification Number: https://doi.org/10.1039/C6RA22340K
Depositing User: Bramwell, Roseanna
Date Deposited: 24 Oct 2016 11:00
Last Modified: 01 Nov 2016 17:49
URI: http://eprints.nottingham.ac.uk/id/eprint/37842

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