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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AC石墨表面接枝Pd(II)-氨基配合物的新型杂化材料: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 π–π stacking of the Ar moiety and the graphene planes of the AC, thus favouring the retaining of the metal-complexing 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:报道了一种新的制备基于固体Pd(II)的催化剂的方法,该方法由在活性炭(AC)表面上固定设计的Pd(II)配合物组成。 F不同的两个Ar–S–F型分子(其中Ar为平面嘧啶部分,F为Pd(II)-配体,S为脂肪族连接基)通过π–π堆叠Ar接枝到AC上分子和AC的石墨烯平面,因此有利于保留F的金属络合能力。AC / Ar–S–F杂化物对Pd(II)的吸附是通过F的Pd(II)络合发生的。深入表征,评估了AC / Ar–S–F / Pd(II)杂化物对甲醇中1-辛烯加氢的催化活性。在两种催化剂下,在T = 323.1 K和P = 15 bar时100%转化为正辛烷,大部分Pd(II)还原为Pd(0)纳米颗粒,并保留在AC表面。在三个额外的循环中重复使用催化剂表明,带有F配体且具有更大的Pd络合能力的催化剂没有显示出活性损失(100%转化为正辛烷),这归因于其较大的结构稳定性。由于Pd(0)纳米粒子的不断聚集,具有较弱F配体的催化剂活性逐渐降低(在四个循环中从100%降至79%)。 T = 303.1 K和P = 1.5 bar的较温和条件阻止了Pd(0)纳米粒子在该催化剂中的聚集,从而允许在四个反应周期中保持高催化效率(100%转化率)。

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