Self-Assembly of a Carboxyl-Functionalized BODIPY Dye via Hydrogen Bonding

We report the synthesis, characterization, and self-assembly behavior of a 4,4-Difluoro-4-bora-3a,4a-diaza-<i>s</i>-indacene (BODIPY) dye functionalized at the <i>meso</i>-position with a butyric acid group. Various spectroscopic investigations (UV-Vis, emission, and Fourier-...

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Bibliographic Details
Main Authors: Beatriz Matarranz, Angel Sampedro, Constantin G. Daniliuc, Gustavo Fernández
Format: Article
Language:English
Published: MDPI AG 2018-11-01
Series:Crystals
Subjects:
Online Access:https://www.mdpi.com/2073-4352/8/11/436
Description
Summary:We report the synthesis, characterization, and self-assembly behavior of a 4,4-Difluoro-4-bora-3a,4a-diaza-<i>s</i>-indacene (BODIPY) dye functionalized at the <i>meso</i>-position with a butyric acid group. Various spectroscopic investigations (UV-Vis, emission, and Fourier-transform infrared spectroscopy (FTIR) studies) supported by X-ray analysis revealed the formation of self-assembled structures in the solid state with translationally stacked BODIPY units driven by hydrogen bonding between the carboxyl groups.
ISSN:2073-4352