Loading…

Visible-light photocatalytic selective aerobic oxidation of thiols to disulfides on anatase TiO2

This work presents the visible-light photocatalytic selective oxidation of thiols to disulfides with molecular oxygen (O2) on anatase TiO2. The high specific surface area of anatase TiO2 proved to be especially critical in conferring high photocatalytic activity. Herein, surface complexation between...

Full description

Saved in:
Bibliographic Details
Published in:Chinese journal of catalysis 2020-10, Vol.41 (10), p.1468-1473
Main Authors: Xu, Hui, Shi, Ji-Long, Lyu, Shaoshuai, Lang, Xianjun
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:This work presents the visible-light photocatalytic selective oxidation of thiols to disulfides with molecular oxygen (O2) on anatase TiO2. The high specific surface area of anatase TiO2 proved to be especially critical in conferring high photocatalytic activity. Herein, surface complexation between thiol and TiO2 gives rise to photocatalytic activity under irradiation with 520 nm green light-emitting diodes (LEDs), resulting in excellent reaction activity, substrate scope, and functional group tolerance. The transformation was extremely efficient for the selective oxidation of various thiols, particularly with substrates bearing electron-withdrawing groups (reaction times of less than 10 min). To date, the longest wavelength of visible light that this system can utilize is 520 nm by the surface complex of substrate-TiO2. Importantly, O2 was found to act as the electron and proton acceptor, rather than to incorporate into the substrates. Our findings regarding this surface complex-based photocatalytic system can allow one to understand the interaction between the conduction band electrons and O2. Surface complex formed between thiols and TiO2 gives rise to visible-light photocatalytic activity, leading to excellent reaction activity, substrate scope, and functional group tolerance under 520 nm LED irradiation.
ISSN:1872-2067
1872-2067
DOI:10.1016/S1872-2067(20)63640-3