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Crystals 2018, 8(11), 436; https://doi.org/10.3390/cryst8110436

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

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraße, 40, 48149 Münster, Germany
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Received: 19 October 2018 / Revised: 15 November 2018 / Accepted: 16 November 2018 / Published: 20 November 2018
(This article belongs to the Special Issue Self-Assembled Supramolecular Polymers via Strong H Bonding)
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Abstract

We report the synthesis, characterization, and self-assembly behavior of a 4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dye functionalized at the meso-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. View Full-Text
Keywords: BODIPY dyes; hydrogen bonding; Self-Assembly; weak non-covalent interactions BODIPY dyes; hydrogen bonding; Self-Assembly; weak non-covalent interactions
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Matarranz, B.; Sampedro, A.; G. Daniliuc, C.; Fernández, G. Self-Assembly of a Carboxyl-Functionalized BODIPY Dye via Hydrogen Bonding. Crystals 2018, 8, 436.

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