Fundamental Study of the Optical and Vibrational Properties of Fx-AZBMOF systems as Functions of Dye Substitution and the Loading Amount

Controlling the switching efficiency of photoactive hybrid systems is an obligatory key prerequisite for systematically improving the design of functional materials. By modulating the degree of fluorination and the amount being embedded into porous hosts, the E/Z ratios of fluorinated azobenzenes we...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 38(2022), 14 vom: 12. Apr., Seite 4295-4309
1. Verfasser: Rödl, Markus (VerfasserIn)
Weitere Verfasser: Reka, Alen, Panic, Marko, Fischereder, Alexander, Oberlechner, Marco, Mairegger, Thomas, Kopacka, Holger, Huppertz, Hubert, Hofer, Thomas S, Schwartz, Heidi A
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't
Beschreibung
Zusammenfassung:Controlling the switching efficiency of photoactive hybrid systems is an obligatory key prerequisite for systematically improving the design of functional materials. By modulating the degree of fluorination and the amount being embedded into porous hosts, the E/Z ratios of fluorinated azobenzenes were adjusted as both functions of substitution and the degree of loading. Octafluoroazobenzene (F8-AZB) and perfluoroazobenzene (F10-AZB) were inserted into porous DMOF-1. Especially for perfluoroazobenzene (F10-AZB), an immense stabilization of the E isomer was observed. In complementary molecular dynamics simulations performed at the DFTB (density functional tight binding) level, an in-depth characterization of the interactions of the different photoisomers and the host structure was carried out. On the basis of the resulting structural and energetic data, the experimentally observed increase in the amount of the Z conformer for F8-AZB can be explained, while the stabilization of E-F10-AZB can be directly related to a fundamentally different interaction motif compared to its tetra- and octafluorinated counterparts
Beschreibung:Date Completed 13.04.2022
Date Revised 12.05.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/acs.langmuir.1c03482