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Multistimuli-Responsive Enaminitrile Molecular Switches Displaying H+-Induced Aggregate Emission, Metal Ion-Induced Turn-On Fluorescence, and Organogelation Properties
Royal Institute of Technology.ORCID iD: 0000-0001-5807-8343
Royal Institute of Technology;Hunan Univ, Peoples Republic of China.
Stockholm University.
Stockholm University.
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2018 (English)In: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 140, no 42, p. 13640-13643Article in journal (Refereed) Published
Abstract [en]

Multistimuli-responsive enaminitrile-based configurational switches displaying aggregation-induced emission (AIE), fluorescence turn-on effects, and super gelation properties are presented. The E-isomers dominated (>97%) in neutral/basic solution, and the structures underwent precisely controlled switching around the enamine C=C bond upon addition of acid/base. Specific fluorescence output was observed in response to different external input in the solution and solid states. In response to H+, configurational switching resulted in complete formation of the nonemissive Z-H+-isomers in solution, however displaying deep-blue to blue fluorescence (Phi(F) up to 0.41) in the solid state. In response to Cu-II in the solution state, the E-isomers exhibited intense, turn-on, blue-green fluorescence, which could be turned off by addition of competitive coordination. The acid/base-activated switching, together with the induced AIE-effects, further enabled the accomplishment of a responsive superorganogelator. In nonpolar solvents, a blue-fluorescent supramolecular gel was formed upon addition of acid to the E-isomer suspension. The gelation could be reversed by addition of base, and the overall, reversible process could be repeated at least five cycles.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2018. Vol. 140, no 42, p. 13640-13643
National Category
Biochemistry and Molecular Biology
Research subject
Chemistry, Biochemistry
Identifiers
URN: urn:nbn:se:lnu:diva-78839DOI: 10.1021/jacs.8b09843ISI: 000448755200025PubMedID: 30351138Scopus ID: 2-s2.0-85055124605OAI: oai:DiVA.org:lnu-78839DiVA, id: diva2:1263533
Available from: 2018-11-15 Created: 2018-11-15 Last updated: 2019-08-29Bibliographically approved

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Ramström, Olof

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