催化作用
光催化
硫化物
氧化还原
材料科学
砜
金属有机骨架
选择性
过氧化氢
金属
无机化学
苯甲酸
光化学
化学
有机化学
高分子化学
吸附
冶金
作者
Xiufen Li,Pengfei Wu,Liang Kan,Qian Niu,Shengnan Sun,Qing Huang,Ya‐Qian Lan
标识
DOI:10.1002/adfm.202308534
摘要
Abstract A series of high‐symmetry Th 6 –metal‐organic frameworks (MOFs) are constructed using various metal complex units and the thorium (Th) cluster, and then being applied as a well‐defined catalyst model in the photocatalytic oxidation of methyl phenyl sulfide reactions. The integration of Th 6 ‐MOFs by incorporating metal complex units and redox sites (Th 6 cluster and single‐metal site) can effectively modulate the conversion rate and selectivity. Among them, Ni–PBA–Th 6 (PBA = 4‐pyridin‐4‐yl benzoic acid) achieves up to ≈99% conversion and ≈97% selectivity for methyl phenyl sulfone. Experiments and theoretical calculations further elucidate that Th 6 cluster is the catalytic site for the oxidation of methyl phenyl sulfide to methyl phenyl sulfone, while Ni–PBA is the catalytic site for the reduction of hydrogen peroxide. This work sheds new insight into the structural design and photocatalytic application of more efficient thorium‐based MOF catalysts.
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