Related Experiment Video
Updated: Jan 30, 2026

A Technical Guide for Performing Spectroscopic Measurements on Metal-Organic Frameworks
Published on: April 28, 2023
Selective Photooxidation of Amines and Sulfides Triggered by a Superoxide Radical Using a Novel
Hongxia Wei1, Zhifen Guo1, Xiao Liang1
1Provincial Key Laboratory of Advanced Energy Materials, College of Chemistry , Northeast Normal University , 5268 Renmin Street , Changchun 130024 , China.
Abstract:
Photocatalysis is an efficient and sustainable approach to convert solar energy into chemical energy, simultaneously supplying valuable chemicals. In this study, a novel metal-organic framework (MOF) compound is constructed from anthracene-based organic linkers, which shows visible-light absorption and efficient photoinduced charge generation property. It was applied for triggering photooxidation of benzylamines and sulfides in the presence of environmental benign oxidants of molecular oxygen or hydrogen peroxide. Results show that it is a highly selective photocatalyst for oxidation reactions to produce valuable imines or sulfoxides. We further investigate the underlying mechanism for these photocatalytic reactions by recognizing reactive oxygen species in the reactions. It has been demonstrated that the superoxide radical (O2•-), generated by electron transfer from a photoexcited MOF to oxidants, serves as the main active species for the oxidations. The work demonstrates the great potential of photoactive MOFs for the transformation of organic chemicals into valuable complexes.
Related Concept Videos
Photoreceptors and Plant Responses to Light
Dose-Response Relationship: Selectivity and Specificity
Preparation and Reactions of Sulfides
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
Alkali Metals
Table 1: Properties of the alkali metals
Structure and Nomenclature of Thiols and Sulfides

