Highly efficient oxidation of various thioethers with molecular oxygen catalyzed by bimetallic SnMo-MOF

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL
Haotian Guo , Xinhuan Lu , Wang Zhang , Meiling Zhang , Lin Zhao , Dan Zhou , Qinghua Xia
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引用次数: 0

Abstract

Bimetallic or polymetallic materials often exhibit different catalytic activities due to the interaction between different metal centers compared with monometallic materials. Here, we designed and synthesized a new bimetallic catalyst SnMo-MOF with tin and molybdenum as metal centers by solvothermal synthesis, which could realize the oxidation of diphenyl sulfide (Ph2S) and difurfuryl sulfide (FFS) under mild conditions, and selectively generate sulfoxide and sulfone, respectively. The introduction of Sn enhanced the Lewis acidity of the catalyst surface and the electron transfer between Sn and Mo led to bimetallic synergistic catalysis, which made a great contribution to the high conversion and selectivity of sulfide oxidation. This is reflected in the complete conversion of Ph2S and FFS with 91.8% and 98.1% selectivity of diphenyl sulfoxide (Ph2SO) and difurfuryl sulfone (FFSO2), respectively. The composite material had good substrate adaptability for the catalytic oxidation of other phenyl sulfides and furfuryl sulfides, which opens interesting prospects for the development of new MOF materials as efficient heterogeneous catalysts for the oxidation of thioethers.

Abstract Image

双金属 SnMo-MOF 催化分子氧高效氧化各种硫醚
与单金属材料相比,双金属或多金属材料往往因不同金属中心之间的相互作用而表现出不同的催化活性。在此,我们以锡和钼为金属中心,通过溶热合成法设计并合成了一种新型双金属催化剂 SnMo-MOF,它能在温和条件下实现二苯硫醚(Ph2S)和二糠基硫醚(FFS)的氧化,并分别选择性地生成亚砜和砜。Sn 的引入增强了催化剂表面的路易斯酸性,Sn 与 Mo 之间的电子传递产生了双金属协同催化作用,为硫化物氧化的高转化率和高选择性做出了巨大贡献。这体现在 Ph2S 和 FFS 的完全转化上,二苯基亚砜(Ph2SO)和二糠基砜(FFSO2)的选择性分别为 91.8% 和 98.1%。该复合材料对其他苯基硫化物和糠基硫化物的催化氧化具有良好的底物适应性,这为开发新型 MOF 材料作为硫醚氧化的高效异相催化剂开辟了有趣的前景。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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