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Catalytic behaviour of a novel Fe(III) Schiff base complex in the mild oxidation of cyclohexane

机译:新型Fe(III)Schiff碱基复合物的催化行为在环己烷的轻度氧化中

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The complex [Fe-III(HL)Cl-2(DMF)]Cl.DMF (1) was synthesized by reaction of Fe(III) chloride with a dimethylformamide solution of the Schiff base aminoalcohol HL (2-[(E)-{[2-(piperazin-1-yl)ethyl]imino}-methyl]phenol) and characterized by single crystal X-ray diffraction analysis, thermogravimetry and spectroscopic methods. The catalytic investigations disclosed a marked activity of 1 towards oxidation of cyclohexane with hydrogen peroxide, under mild conditions, with yields based on cyclohexane up to 37% and TONs (turnover numbers) up to ca. 900. Kinetic experiments and selectivity parameters led to the conclusion that hydroxyl radicals are active (attacking C-H bonds) species in the studied catalytic reaction. Kinetic and UV/Vis spectrometry data revealed a complex nature of the processes occurring in the catalytic system, including the transformation of 1 into catalytically active species.
机译:通过Fe(iii)氯化物与Schiff碱氨基醇HL的二甲基甲酰胺溶液的反应合成复合物[Fe-III(HL)Cl-2(DMF)] Cl.DMF(1)。 {[[2-(哌嗪-1-基)乙基]伊米诺} - 甲基]苯酚,并以单晶体X射线衍射分析,热重法和光谱方法为特征。 该催化研究揭示了在轻度条件下用过氧化氢氧化环己烷的显着活性,其产率基于环己烷的产量高达37%,至Ca。 900.动力学实验和选择性参数得出的结论是,在研究的催化反应中,羟基自由基是活性(攻击C-H键)物种。 动力学和紫外线/VIS光谱学数据揭示了催化系统中发生的过程的复杂性质,包括将1转化为催化活性物质。

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