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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Diruthenium(II,III) tetramidates as a new class of oxygenation catalysts
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Diruthenium(II,III) tetramidates as a new class of oxygenation catalysts

机译:四酰亚胺钌(II,III)作为新型的氧化催化剂

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Two new diruthenium(II,III) tetramidate compounds, Ru _2(NHOCC(CH _3) _2) _4Cl (1) and Ru _2(NHOCCH _2CH _3) _4Cl (2) have been prepared and structurally characterized by X-ray crystallography. The activity of promoting sulfide oxygenation using simple oxidants such as hydrogen peroxide (H _2O _2) and tert-butyl hydroperoxide (TBHP) was studied. A UV-kinetics study indicated that the initial rates of 1 and 2 are comparable to the previously studied diruthenium tetracarboxylates in promoting TBHP oxygenation of methyl phenyl sulfide (MPS). Using excess oxidant and CH _3CN as the solvent, organic sulfides MPS and diphenyl sulfide (PPS) were oxidized using 1 mol% of the catalytic species. Compound 1 is more effective than 2 in converting sulfides to sulfoxide under the same conditions. Fast conversion was achieved when the reactions were carried out in the solvent-free conditions, and the major oxidation product was the sulfoxide. The electronic structure of the title compounds was studied with DFT calculations to gain an understanding of the activation of peroxy reagents.
机译:制备了两个新的四mid酸钌(II,III)化合物Ru _2(NHOCC(CH _3)_2)_4Cl(1)和Ru _2(NHOCCH _2CH _3)_4Cl(2),并通过X射线晶体学对其结构进行了表征。研究了使用简单氧化剂如过氧化氢(H _2O _2)和叔丁基过氧化氢(TBHP)促进硫化物氧合的活性。 UV动力学研究表明,在促进甲基苯基硫醚(MPS)的TBHP氧化中,初始速率1和2与先前研究的四羧酸二钌可比。使用过量的氧化剂和CH _3CN作为溶剂,有机硫化物MPS和二苯硫醚(PPS)使用1 mol%的催化物质进行氧化。在相同条件下,化合物1比2更有效地将硫化物转化为亚砜。当反应在无溶剂条件下进行时,可以实现快速转化,并且主要的氧化产物是亚砜。用DFT计算研究了标题化合物的电子结构,以了解过氧化物试剂的活化。

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