Issue 8, 2019

Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives

Abstract

The development of chiral fluorescent materials has attracted great interest. [1,1′-binaphthalene]-2,2′-diol (BINOL), a privileged C2-symmetric molecular skeleton, is one of the most frequently used chiral optical backbones. However, a phenomenon of circular dichroism (CD) annihilation in the aggregated state was observed in BINOL based molecules, which limits the application of CD in the condensed state. In this work, by inserting various bridged alkyl chains into the hydroxyl groups of 3,3′-dicyanomethylene functionalized (R)-BINOL, a series of chiral luminogens (BINB-n, n = 1 to 8) was obtained. All BINB-n luminogens exhibited aggregation-induced emission (AIE) characteristics and their molecular conformation was significantly dependent on the length of the alkyl chain, which further regulated their CD behavior from annihilation to preservation in the aggregated state. Moreover, in virtue of the AIE characteristic of BINB-6, judiciously introducing suitable electron donors successfully realized enhanced and tunable solid-state circularly polarized luminescence with the maximum glum value of 1 × 10−2.

Graphical abstract: Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
07 май 2019
Accepted
03 юни 2019
First published
04 юни 2019

Mater. Chem. Front., 2019,3, 1613-1618

Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives

N. Zhao, W. Gao, M. Zhang, J. Yang, X. Zheng, Y. Li, R. Cui, W. Yin and N. Li, Mater. Chem. Front., 2019, 3, 1613 DOI: 10.1039/C9QM00292H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements