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首页> 外文期刊>RSC Advances >New hybrid materials based on the grafting of Pd(II)-amino complexes on the graphitic surface of AC: preparation, structures and catalytic properties
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New hybrid materials based on the grafting of Pd(II)-amino complexes on the graphitic surface of AC: preparation, structures and catalytic properties

机译:基于Pd(II)-氨基络合物在AC的石墨表面接枝的新型混合材料:制备,结构和催化性能

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摘要

A novel procedure for the preparation of solid Pd(II)-based catalysts consisting of the anchorage of designed Pd(II)-complexes on an activated carbon (AC) surface is reported. Two molecules of the Ar-S-F type (where Ar is a plane-pyrimidine moiety, F a Pd(II)-ligand and S an aliphatic linker) differing in F, were grafted on AC by pi-pi stacking of the Ar moiety and the graphene planes of the AC, thus favouring the retaining of the metalcomplexing ability of F. Adsorption of Pd(II) by the AC/Ar-S-F hybrids occurs via Pd(II)-complexation by F. After deep characterization, the catalytic activities of the AC/Ar-S-F/Pd(II) hybrids on the hydrogenation of 1-octene in methanol as a catalytic test were evaluated. 100% conversion to n-octane at T = 323.1 K and P = 15 bar, was obtained with both catalysts and most of Pd(II) was reduced to Pd(0) nanoparticles, which remained on the AC surface. Reusing the catalysts in three additional cycles reveals that the catalyst bearing the F ligand with a larger Pd-complexing ability showed no loss of activity (100% conversion to n-octane) which is assigned to its larger structural stability. The catalyst with the weaker F ligand underwent a progressive loss of activity (from 100% to 79% in four cycles), due to the constant aggregation of the Pd(0) nanoparticles. Milder conditions, T = 303.1 K and P = 1.5 bar, prevent the aggregation of the Pd(0) nanoparticles in this catalyst allowing the retention of the high catalytic efficiency (100% conversion) in four reaction cycles.
机译:报道了一种制备具有所设计的Pd(II)的锚固的基于固体Pd(II)的催化剂的新方法 - 在活性炭(Ac)表面上进行复杂。通过在Ar部分的Pi-Pi堆叠接枝在AR中的两个分子的Ar-Sf型(其中Ar是平面 - 嘧啶部分,F a pd(ii)--ligand和s的脂族接头)接枝在Ac上。 AC的石墨烯平面,从而有利于通过F的Pd(II)通过F的Pd(II)通过Pd(II)对Pd(II)的保留剂的保留能力的保留能力。在深度表征后,催化活性评价AC / Ar-SF / Pd(II)杂交物的1-辛烯中作为催化试验的1-辛烯的氢化。在T = 323.1k和p ​​= 15巴下将100%转化为N-辛烷,用催化剂获得,并且将大部分Pd(II)降低至Pd(0)纳米颗粒,其保持在AC表面上。在三个另外的循环中重用催化剂揭示载体具有较大PD络合能力的F配体的催化剂显示出不损失的活性(100%转化为N-辛烷),其分配到其较大的结构稳定性。由于Pd(0)纳米颗粒的恒定聚集,具有较弱的F配体的催化剂进行了逐渐的活性丧失(从四个循环中的100%至79%)。升温条件T = 303.1 k和P = 1.5巴,防止该催化剂中Pd(0)纳米颗粒的聚集,允许在四个反应循环中保留高催化效率(100%转化率)。

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