Issue 7, 2022

A tunable phosphorescence supramolecular switch by an anthracene photoreaction in aqueous solution

Abstract

Purely organic room-temperature phosphorescence (RTP) has attracted tremendous attention, but is rarely reported to possess stimulus responsiveness. Herein, we report a supramolecular RTP switch based on a dicationic guest molecule (BPA) and cucurbituril. BPA possesses a photosensitive 9,10-diphenylanthracene core and terminal 4-(4-bromophenyl)pyridium, which can form 1 : 4 supramolecular assembly with cucurbit[7]uril (CB[7]) and an n : n linear supramolecular polymer with cucurbit[8]uril (CB[8]). The assemblies can exhibit tunable fluorescence emission after undergoing a photoreaction of the anthracene unit in BPA. It is interesting that CB[8] can bind two bromophenylpyridinium units to form a green phosphorescent switch. Notably, the RTP of the assemblies can be reversibly switched on/off by UV irradiation or heating through a tunable Förster resonance energy transfer from 4-(4-bromophenyl)pyridium to anthracene. Moreover, the addition of cucurbituril can significantly accelerate the photoreaction rate of anthracene and enable the assembly to respond quickly to UV irradiation, which expands the application potential of this strategy in stimulus responsive RTP materials.

Graphical abstract: A tunable phosphorescence supramolecular switch by an anthracene photoreaction in aqueous solution

Supplementary files

Article information

Article type
Paper
Submitted
31 Aug 2021
Accepted
25 Okt 2021
First published
25 Okt 2021

J. Mater. Chem. C, 2022,10, 2623-2630

A tunable phosphorescence supramolecular switch by an anthracene photoreaction in aqueous solution

T. Su, Y. Liu, Y. Chen and Y. Liu, J. Mater. Chem. C, 2022, 10, 2623 DOI: 10.1039/D1TC04100B

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