共价键
光催化
氮化碳
三嗪
共价有机骨架
共轭体系
光化学
材料科学
电子顺磁共振
带隙
化学
可见光谱
组合化学
催化作用
聚合物
纳米技术
化学工程
有机化学
高分子化学
光电子学
复合材料
工程类
物理
核磁共振
作者
Huimin Hao,Fulin Zhang,Xiaoyun Dong,Xianjun Lang
标识
DOI:10.1016/j.apcatb.2021.120691
摘要
Triazine, possessing planar and fully conjugated attributes, purveys ample space to construct well-defined crystalline polymers like graphic carbon nitrides (g-C3N4), covalent triazine frameworks (CTFs), and covalent organic frameworks (COFs). Herein, g-C3N4, CTF-1, and TP-COF were successfully synthesized and systematically confirmed by a series of characterizations, aiming at visible light photocatalytic activation of O2. Compared to CTF-1 and g-C3N4, TP-COF was endowed with the best photocatalytic performance by several inherent properties, including a large specific surface area, a suitable bandgap, and superior charge transfer. The blue light-induced selective conversion of organic sulfides has been achieved expeditiously with O2 over TP-COF photocatalyst. Moreover, rigorous control experiments and in situ electron paramagnetic resonance (EPR) suggest that electron and energy transfer pathways contribute to the selective formation of desired sulfoxides. This work emphasizes that the tailor-made trait of COFs provides an ideal plarform of customizing two-dimensional (2D) photoactive COFs based on triazine for visible light-induced selective chemical transformations.
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