Issue 16, 2019

A supramolecular assembly bearing an organic TADF chromophore: synthesis, characterization and light-driven cooperative acceptorless dehydrogenation of secondary amines

Abstract

A noble-metal-free chromophore–catalyst supramolecular assembly, which is composed of an organic thermally activated delayed fluorescence (TADF) chromophore and cobaloximes, has been designed and synthesized for the first time for the efficient acceptorless dehydrogenation of secondary amines under blue light irradiation at room temperature. The TADF chromophore has a long lifetime of 17.4 μs with suitable redox potentials for the selective acceptorless dehydrogenation of secondary amines to afford imines and H2 through cooperative catalysis of the chromophore and cobaloximes in the supramolecular assembly. A high TON of 895 was obtained for the acceptorless dehydrogenation of 1,2,3,4-tetrahydroisoquinoline despite its high oxidation potential (+1.38 V vs. SCE).

Graphical abstract: A supramolecular assembly bearing an organic TADF chromophore: synthesis, characterization and light-driven cooperative acceptorless dehydrogenation of secondary amines

Supplementary files

Article information

Article type
Paper
Submitted
29 Jan 2019
Accepted
25 Mar 2019
First published
25 Mar 2019

Dalton Trans., 2019,48, 5444-5449

A supramolecular assembly bearing an organic TADF chromophore: synthesis, characterization and light-driven cooperative acceptorless dehydrogenation of secondary amines

D. Chao and M. Zhao, Dalton Trans., 2019, 48, 5444 DOI: 10.1039/C9DT00407F

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