In situ electrochemical investigations of inherently chiral 2,2′‐biindole architectures with oligothiophene terminals

Malacrida, Claudia; Scapinello, Luca; Cirilli, Roberto; Grecchi, Sara; Penoni, Andrea; Benincori, Tiziana; Ludwigs, Sabine

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DC Element	Wert	Sprache
dc.contributor.author	Malacrida, Claudia	-
dc.contributor.author	Scapinello, Luca	-
dc.contributor.author	Cirilli, Roberto	-
dc.contributor.author	Grecchi, Sara	-
dc.contributor.author	Penoni, Andrea	-
dc.contributor.author	Benincori, Tiziana	-
dc.contributor.author	Ludwigs, Sabine	-
dc.date.accessioned	2024-04-29T11:54:48Z	-
dc.date.available	2024-04-29T11:54:48Z	-
dc.date.issued	2021	de
dc.identifier.issn	2196-0216	-
dc.identifier.other	1887374434	-
dc.identifier.uri	http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-143154	de
dc.identifier.uri	http://elib.uni-stuttgart.de/handle/11682/14315	-
dc.identifier.uri	http://dx.doi.org/10.18419/opus-14296	-
dc.description.abstract	The synthesis and characterization of three new inherently chiral N,N′‐dipropyl‐3,3′‐diheteroaryl‐2,2′‐biindole monomers, nicknamed Ind2T4, Ind2T6 and Ind2Ph2T4, which differ in the number of thiophenes as terminals, are reported. In addition to a full monomer characterization, stable electroactive oligomeric films were obtained by electro‐oxidation upon cycling to potentials which activate the thiophene terminals. Cyclic voltammetry, UV‐Vis‐NIR spectroelectrochemistry and in situ conductance measurements show that oligomeric films of Ind2T6 present the best stability and electrochromic switching performance. Enantioselective tests with a chiral ferrocene amine clearly show the potential as chiral selectors for analytical and sensing purposes.	en
dc.description.sponsorship	Integrated Quantum Science and Technology	de
dc.description.sponsorship	Carl-Zeiss-Foundation	de
dc.description.sponsorship	Ministero dell’Istruzione, Università e Ricerca	de
dc.description.sponsorship	Projekt DEAL	de
dc.language.iso	en	de
dc.relation.uri	doi:10.1002/celc.202100511	de
dc.rights	info:eu-repo/semantics/openAccess	de
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/	de
dc.subject.ddc	540	de
dc.subject.ddc	621.3	de
dc.title	In situ electrochemical investigations of inherently chiral 2,2′‐biindole architectures with oligothiophene terminals	en
dc.type	article	de
dc.date.updated	2023-11-14T02:57:22Z	-
ubs.fakultaet	Chemie	de
ubs.fakultaet	Fakultätsübergreifend / Sonstige Einrichtung	de
ubs.institut	Institut für Polymerchemie	de
ubs.institut	Fakultätsübergreifend / Sonstige Einrichtung	de
ubs.publikation.seiten	3250-3261	de
ubs.publikation.source	ChemElectroChem 8 (2021), S. 3250-3261	de
ubs.publikation.typ	Zeitschriftenartikel	de
Enthalten in den Sammlungen:	03 Fakultät Chemie

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