Wavelength Selective Photocontrol of Hybrid Azobenzene-Spiropyran Photoswitches with Overlapping Chromophores

dc.contributor.authorSaßmannshausen, Torben
dc.contributor.authorKunz, Anne
dc.contributor.authorOberhof, Nils
dc.contributor.authorSchneider, Friederike
dc.contributor.authorSlavov, Chavdar
dc.contributor.authorDreuw, Andreas
dc.contributor.authorWachtveitl, Josef
dc.contributor.authorWegner, Hermann A.
dc.date.accessioned2024-11-22T14:09:09Z
dc.date.available2024-11-22T14:09:09Z
dc.date.issued2024
dc.description.abstractCompounds with multiple photoswitching units are appealing for complex photochemical control of molecular materials and nanostructures. Herein, we synthesized novel meta- and para- connected (related to the nitrogen of the indoline) azobenzene-spiropyran dyads, in which the central benzene unit is shared by both switches. We investigated their photochemistry using static and time-resolved transient absorption spectroscopy as well as quantum chemical calculations. In the meta-compound, the individual components are photochemically decoupled due to the meta-pattern. In the para-compound the spiro-connectivity leads to a bifunctional photoswitchable system with a red-shifted absorption. The azobenzene and the spiropyran can thus be addressed and switched independently by light of appropriate wavelength. Through the different connectivity patterns two different orthogonally photoswitchable systems have been obtained which are promising candidates for complex applications of light control.en
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG); ROR-ID:018mejw64
dc.identifier.urihttps://jlupub.ub.uni-giessen.de/handle/jlupub/19894
dc.identifier.urihttps://doi.org/10.22029/jlupub-19249
dc.language.isoen
dc.rightsNamensnennung - Nicht kommerziell 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subject.ddcddc:540
dc.titleWavelength Selective Photocontrol of Hybrid Azobenzene-Spiropyran Photoswitches with Overlapping Chromophores
dc.typearticle
local.affiliationFB 08 - Biologie und Chemie
local.projectFOR 5499, project 496207555; WA 1850/4-3
local.source.articlenumbere202314112
local.source.journaltitleAngewandte Chemie. International edition
local.source.number10
local.source.urihttps://doi.org/10.1002/anie.202314112
local.source.volume63

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