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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Quantitation of the ligand effect in oxo-transfer reactions of dioxo-Mo(vi) trispyrazolyl borate complexes
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Quantitation of the ligand effect in oxo-transfer reactions of dioxo-Mo(vi) trispyrazolyl borate complexes

机译:定量的二氧杂-Mo(vi)三吡唑基硼酸酯配合物的羰基转移反应中的配体效应

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The oxygen atom transfer reactivity (OAT) of dioxo-Mo(vi) complexes of hydrotrispyrazolyl borate (hydrotris(3,5-dimethylpyrazolyl)borate, Tp M~(e2); hydrotris(3-isopropylpyrazol-1-yl)borate, Tp~(iPr)) with tertiary phosphines (PMe_3, PMe_2Ph, PEt_3, PEt_2Ph, PBu~n _3, PMePh_2, or PEtPh _2) has been investigated. In acetonitrile, these reactions proceed via the formation of a phosphoryl intermediate complex that undergoes a solvolysis reaction. We report the synthesis and characterization of several phosphoryl complexes. The rates of formation of phosphoryl complexes and their solvation were determined by spectrophotometry. The rates of the reactions and the properties of the phosphoryl species were investigated using the Quantitative Analysis of Ligand Effect (QALE) methodology. The results show that, at least in this system, the first step of the reaction is controlled primarily by the steric factor, and in the second step, both electronic and steric factors are important. We also analyzed the effect of ligands on the reaction rate i.e., Tp~(Me2)vs. Tp~(iPr).
机译:氢三吡唑基硼酸酯(氢三(3,5-二甲基吡唑基)硼酸酯,TP M〜(e2);氢三(3-异丙基吡唑-1-基)硼酸酯,TP)的二氧-Mo(vi)配合物的氧原子转移反应性(OAT)已经研究了具有叔膦(PMe_3,PMe_2Ph,PEt_3,PEt_2Ph,PBu〜n _3,PMePh_2或PEtPh _2)的〜(iPr))。在乙腈中,这些反应通过形成发生溶剂分解反应的磷酰基中间体配合物而进行。我们报告了几种磷酰基复合物的合成和表征。磷酰基复合物的形成速率及其溶剂化通过分光光度法测定。使用配体效应定量分析(QALE)方法研究了反应速率和磷酰基物质的性质。结果表明,至少在该系统中,反应的第一步主要受空间因素控制,而在第二步中,电子和空间因素均很重要。我们还分析了配体对反应速率即Tp〜(Me2)vs的影响。 Tp〜(iPr)。

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