Flavin-Helicene Amphiphilic Hybrids: Synthesis, Characterization, and Preparation of Surface-Supported Films

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Publikace nespadá pod Filozofickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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JAKUBEC Martin NOVÁK David ZATLOUKALOVÁ Martina CÍSAŘOVÁ Ivana CIBULKA Radek FAVEREAU Ludovic CRASSOUS Jeanne CYTRYNIAK Adrianna BILEWICZ Renata HRBÁČ Jan STORCH Jan ŽÁDNÝ Jaroslav VACEK Jan

Rok publikování 2021
Druh Článek v odborném periodiku
Časopis / Zdroj ChemPlusChem
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cplu.202100092
Doi http://dx.doi.org/10.1002/cplu.202100092
Klíčová slova flavins; helicenes; lipidic cubic phases; redox behavior; thin layers
Popis This work reports on the preparation and structural characterization of flavo[7]helicene 1 (flavin-[7]helicene conjugate), which was subsequently characterized at the molecular level in either an aqueous environment or an organic phase, at the supramolecular level in the form of polymeric layers, and also embedded in a lipidic mesophase environment to study the resulting properties of such a hybrid relative to its parent molecules. The flavin benzo[g]pteridin-2,4-dione (isoalloxazine) was selected for conjugation because of its photoactivity and reversible redox behavior. Compound 1 was prepared from 2-nitroso[6]helicene and 6-methylamino-3-methyluracil, and characterized using common structural and spectroscopic tools: circular dichroism (CD), circularly polarized luminescence (CPL) spectroscopy, cyclic voltammetry (CV), and DFT quantum calculations. In addition, a methodology that allows the loading of 1 enantiomers into an internally nanostructured lipid (1-monoolein) matrix was developed.
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