Identification of the irreversible redox behavior of highly fluorescent benzothiadiazoles

dc.contributor.authorRietsch, Philipp
dc.contributor.authorSobottka, Sebastian
dc.contributor.authorHoffmann, Katrin
dc.contributor.authorHildebrandt, Pascal
dc.contributor.authorSarkar, Biprajit
dc.contributor.authorResch‐Genger, Ute
dc.contributor.authorEigler, Siegfried
dc.date.accessioned2024-04-26T11:04:36Z
dc.date.available2024-04-26T11:04:36Z
dc.date.issued2020de
dc.date.updated2023-11-14T06:17:10Z
dc.description.abstractRedox switches are applied in various fields of research, including molecular lifts, electronic devices and sensors. Switching the absorbance between UV and Vis/NIR by redox processes is of interest for applications in light harvesting or biomedicine. Here, we present a series of push‐pull benzothiadiazole derivatives with high fluorescence quantum yields in solution and in the crystalline solid state. Spectroelectrochemical analysis reveals the switching of UV‐absorption in the neutral state to Vis/NIR absorption in the reduced state. We identify the partial irreversibility of the switching process, which appears to be reversible on the cyclic voltammetry timescale.en
dc.description.sponsorshipDFGde
dc.identifier.issn2367-0932
dc.identifier.other1887445552
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-143012de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/14301
dc.identifier.urihttp://dx.doi.org/10.18419/opus-14282
dc.language.isoende
dc.relation.uridoi:10.1002/cptc.202000050de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subject.ddc540de
dc.titleIdentification of the irreversible redox behavior of highly fluorescent benzothiadiazolesen
dc.typearticlede
ubs.fakultaetChemiede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutInstitut für Anorganische Chemiede
ubs.institutFakultätsübergreifend / Sonstige Einrichtungde
ubs.publikation.seiten668-673de
ubs.publikation.sourceChemPhotoChem 4 (2020), S. 668-673de
ubs.publikation.typZeitschriftenartikelde

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
CPTC_CPTC202000050.pdf
Size:
1.59 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
3.3 KB
Format:
Item-specific license agreed upon to submission
Description: