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Mn-containing porous silicates as catalysts for the solvent-free selective oxidation of alkyl aromatics to aromatic ketones with molecular oxygen

机译:含锰的多孔硅酸盐作为催化剂,用于利用分子氧将烷基芳烃无溶剂选择性氧化为芳族酮

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摘要

Mn-containing redox molecular sieves, i.e., highly crystalline microporous MnS-1 (0.6 wt% Mn, n(Si)/ n(Mn) = 160) and ordered mesoporous silicates MnMCM-41 and MnMCM-48 (1.8 wt% Mn, n(Si)/ n(Mn) = 51), were synthesized. The porosity of the products was determined by X-ray powder diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). The evidence for the presence of isolated Mn sites incorporated into the silicate framework was obtained by Mn K-edge XANES and EXAFS analysis, which provided direct information on valence state and local environment of Mn in these products. The analysis revealed the presence of predominantly Mn~(3+) cations located at a 3-fold coordination in the silicate framework indicating Lewis acid sites in microporous (MnS-1) and mesoporous (MnMCM-41, MnMCM-48) silicate structures. The micro- and mesoporous silicates containing framework Mn~(3+)-sites selectively catalyze the oxidation of alkyl aromatics in benzylic position to aromatic ketones in the absence of any initiator using molecular oxygen as the terminal oxidant under mild, solvent-free, liquid-phase conditions.
机译:含Mn的氧化还原分子筛,即高结晶微孔MnS-1(0.6 wt%Mn,n(Si)/ n(Mn)= 160)和有序中孔硅酸盐MnMCM-41和MnMCM-48(1.8 wt%Mn,合成n(Si)/ n(Mn)= 51)。通过X射线粉末衍射(XRD)和高分辨率透射电子显微镜(HRTEM)确定产物的孔隙率。通过Mn K-edge XANES和EXAFS分析获得了并入硅酸盐骨架中的孤立Mn位点的证据,这些分析提供了有关这些产品中Mn的价态和局部环境的直接信息。分析表明,主要的Mn〜(3+)阳离子位于硅酸盐骨架的3倍配位处,表明路易斯酸位在微孔(MnS-1)和中孔(MnMCM-41,MnMCM-48)硅酸盐结构中。在没有任何引发剂的情况下,使用分子氧作为末端氧化剂,在温和,无溶剂,液态的条件下,含有骨架Mn〜(3 +)-位的微孔和中孔硅酸盐选择性催化苄基位置的烷基芳族化合物氧化为芳族酮相条件。

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