Issue 1, 2022

Photoactive perylenediimide metal–organic framework for boosting iodoperfluoroalkylation of alkenes and oxidative coupling of amines

Abstract

The incorporation of photoactive units into metal–organic frameworks (MOFs) is of particular interest due to their ability to endow the MOFs with additional properties such as photomagnetism, photomodulated electrical conductivity, and photocatalytic properties. Perylenediimides (PDIs), as a class of organic dye molecules with strong visible-light absorption ability and high photochemical activity, have attracted considerable interest because of their consecutive photoinduced electron transfer processes for the generation of energetic PDI radical anions. In this context, a novel photoactive MOF based on a perylenediimide derivative, Zn2(diPyPI-Cl4)(NDC)2·3DMF (MOF 1) (diPyPI-Cl4 = N,N′-bis(pyridyl)-1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxy bisimide, H2NDC = 2,6-naphthalenedicarboxylic acid), has been successfully constructed, which exhibits a porous three-dimensional framework with a pcu topology. MOF 1 that acts as an efficient and recyclable electron-transfer photocatalyst is applied for boosting the iodoperfluoroalkylation of alkenes and oxidation of amines to imines under mild conditions with high yields and excellent substrate application ranges. This photocatalyst has the advantages of high efficiency, low catalytic loading and easy availability, which is highly feasible from a synthetic point of view.

Graphical abstract: Photoactive perylenediimide metal–organic framework for boosting iodoperfluoroalkylation of alkenes and oxidative coupling of amines

Supplementary files

Article information

Article type
Research Article
Submitted
23 9 2021
Accepted
04 11 2021
First published
05 11 2021

Inorg. Chem. Front., 2022,9, 111-118

Photoactive perylenediimide metal–organic framework for boosting iodoperfluoroalkylation of alkenes and oxidative coupling of amines

Z. Liu, C. Li, J. Chen, X. Li, F. Luo, F. Cheng and J. Liu, Inorg. Chem. Front., 2022, 9, 111 DOI: 10.1039/D1QI01206A

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