A Fully Conjugated Benzo[1,2-b:4,5-b']dithiophene-Based Covalent Organic Framework Enables Efficient Blue Light-Driven Photocatalytic Sulfoxidation.

Abstract

Covalent organic frameworks (COFs) are becoming increasingly attractive in photocatalytic transformations because of the designable structures grounded on the building blocks and the linkage. Herein, benzo[1,2-b:4,5-b']dithiophene, essential for various organic optoelectronic materials, is adopted as the building block for COFs. Hence, a fully conjugated COF BDTT-sp2c-COF and imine-linked COF BDTT-COF are constructed of 5',5''''-(benzo[1,2-b:4,5-b']dithiophene-2,6-diyl)bis([1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde) with p-phenyldiacetonitrile and p-phenylenediamine, respectively. Thorough characterizations and theoretical calculations disclose that BDTT-sp2c-COF is superior to BDTT-COF in terms of specific surface area, photocarrier separation, and electron transfer. As such, BDTT-sp2c-COF enables more efficient photocatalytic sulfoxidation with oxygen than BDTT-COF. The fully conjugated structure guarantees the recyclability of BDTT-sp2c-COF. The blue light-driven sulfoxidation is generally applicable and proceeds selectively via energy and electron transfers over BDTT-sp2c-COF. The fully conjugated COFs are promising to enable photocatalytic reactions.