Issue 55, 2019

Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes

Abstract

By combining the fluorophores of axially chiral 1,1′-binaphthol (BINOL) and 1,4-dihydropyridine derivatives, axially chiral 1,4-dihydropyridine derivatives ((R)-/(S)-2) with aggregation-induced emission (AIE) in exciplexes were designed and synthesized. (R)-/(S)-2 emitted low fluorescence in THF solutions of their locally excited states; however, they emitted red-shifted fluorescence in the aggregate state upon exciplex formation. Moreover, (R)-/(S)-2 showed linear and multi-exponential relationships between their local excited and exciplex fluorescence intensities and the viscosity of the medium, which allowed us to determine the viscosities of different mixed solvents. In addition, as an axially chiral viscosity probe, (R)-/(S)-2 show excellent CD signals and have potential applications in the fields of chiral recognition and fluorescence imaging, which will broaden the new family of AIE fluorophores. To the best of our knowledge, there are few reports of axially chiral intramolecular exciplex-mediated AIE molecules.

Graphical abstract: Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug 2019
Accepted
25 Sep 2019
First published
10 Oct 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 32219-32225

Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes

Z. Yang, Y. Huo, Y. Liu, G. Du, W. Zhang, L. Zhou, L. Zhan, X. Ren, W. Duan and S. Gong, RSC Adv., 2019, 9, 32219 DOI: 10.1039/C9RA06553A

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