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Catalytic Activity of Polynuclear vs. Dinuclear Aroylhydrazone Cu(II) Complexes in Microwave-Assisted Oxidation of Neat Aliphatic and Aromatic Hydrocarbons

机译:多核芳酰肼酮催化活性的多核芳酰肼Cu(II)络合物在微波辅助氧化氮氧化物和芳烃中的微波辅助氧化

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摘要

One-dimensional (1D) polynuclear Cu(II) complex (1) derived from (5-bromo-2-hydroxybenzylidene)-2-hydroxybenzohydrazide (H2L) is synthesized and characterized by elemental analysis, IR spectroscopy, ESI-MS, and single crystal X-ray crystallography. Its catalytic performance towards the solvent-free microwave-assisted peroxidative oxidation of aliphatic and aromatic hydrocarbons under mild conditions is compared with that of dinuclear Cu(II) complexes (2 and 3) of the same ligand, previously reported as antiproliferative agents. Polymer 1 exhibits the highest activity, either for the oxidation of cyclohexane (leading to overall yields, based on the alkane, of up to 39% of cyclohexanol and cyclohexanone) or towards the oxidation of toluene (selectively affording benzaldehyde up to a 44% yield), after 2 or 2.5 h of irradiation at 80 or 50 degrees C, respectively.
机译:衍生自(5-溴-2-羟基苄基苄基)-2-羟基苯甲酰肼(H2L)的一维(1D)多核Cu(II)复合物(1)由元素分析,红外光谱,ESI-MS和单一的组成和特征合成并表征 晶体X射线晶体学。 将其在温和条件下,将其朝向无溶剂微波辅助过氧化氧化的催化性能与相同配体的二核Cu(II)配合物(2和3)的脂肪族和芳族烃进行比较,以前称为抗增殖剂。 聚合物1表现出最高的活性,用于氧化环己烷(导致基于烷烃的总体产率,高达39%的环己醇和环己酮)或朝向甲苯的氧化(选择性地提供苯甲醛,高达44%收率44% ),在80或50摄氏度的照射后2或2.5小时后。

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