Visible-Light-Responsive 2D Photocatalysts Assembled by Evans–Showell-Type POMs and Metalloviologen Frameworks for Sulfide–Sulfoxide Transformation

化学 亚砜 硫化物 光催化 催化作用 多金属氧酸盐 电子转移 光化学 有机化学
作者
Yanhong Chen,Haiyan An,Shenzhen Chang,Tieqi Xu,Yanqin Li,Qingshan Zhu,Yao-Hui Huang,Yuting Wei
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:62 (26): 10120-10130 被引量:18
标识
DOI:10.1021/acs.inorgchem.3c00565
摘要

Sulfide–sulfoxide aerobic photo-oxidation is of great interest in organic and medicinal chemistry; however, developing efficient and facile heterogeneous photocatalytic systems without additional additives remains challenging. Herein, we intentionally designed and synthesized two polyoxometalate (POM)-based metalloviologen frameworks, formulated as [MII(4-PBPY)2(H2O)][MII(H2O)4][CoIII2MoVI10H4O38]·nH2O (M = Cu, n = 10 for 1; M = Co, n = 11 for 2), prepared by the mild one-step synthesis strategy and characterized in detail. X-ray single-crystal diffraction analysis shows that they present a two-dimensional layered structure formed by two parallel metalloviologen layers pillared by dimeric Evans–Showell-type POMs. The connection of POM to the metalloviologen framework enables easier flow of electrons to the POM port, which can theoretically further induce O2 to generate reactive oxygen species (O2•–) to oxidize substrates to form target products. As expected, both 1 and 2 exhibit outstanding photocatalytic activity in the oxidation of sulfides. Within 6 h, methyl phenyl sulfide can be quantitatively converted into methyl phenyl sulfoxide. The in-depth mechanism reveals that there is also a synergistic energy-transfer pathway in the catalytic system in addition to the electron-transfer pathway. In addition, the corresponding catalytic activity and structure can be well maintained after at least 10 cycle experiments.
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