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首页> 外文期刊>Journal of the American Chemical Society >Orthophosphate and Sulfate Utilization for C-E (E = P, S) Bond Formation via Trichlorosilyl Phosphide and Sulfide Anions
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Orthophosphate and Sulfate Utilization for C-E (E = P, S) Bond Formation via Trichlorosilyl Phosphide and Sulfide Anions

机译:正磷酸盐和硫酸盐通过三氯甲硅烷基磷和硫化物阴离子形成C-E(E = P,S)键

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摘要

Reduction of phosphoric acid (H3PO4) or tetra-n-butylammonium bisulfate ([TBA][HSO4]) with trichlorosilane leads to the formation of the bis(trichlorosilyl)phosphide ([P(SiCl3)(2)](-), 1) and trichlorosilylsulfide ([Cl3SiS](-), 2) anions, respectively. Balanced equations for the formation of the TBA salts of anions 1 and 2 were formulated based on the identification of hexachlorodisiloxane and hydrogen gas as byproducts arising from these reductive processes: i) [H2PO4](-) + 10HSiCl(3) - 1 + 4O(SiCl3)(2) + 6H(2) for P and ii) [HSO4](-) + 9HSiCl(3) - 2 + 4O(SiCl3)(2) + 5H(2) for S. Hydrogen gas was identified by its subsequent use to hydrogenate an alkene ((-)-terpinen-4-ol) using Crabtree's catalyst ([(COD)Ir(py)-(PCy3)] [PF6], COD = 1,5-cyclooctadiene, py = pyridine, Cy = cyclohexyl). Phosphide 1 was generated in situ by the reaction of phosphoric acid and trichlorosilane and used to convert an alkyl chloride (1-chlorooctane) to the corresponding primary phosphine, which was isolated in 41% yield. Anion 1 was also prepared from [TBA] [H2PO4] and isolated in 62% yield on a gram scale. Treatment of [TBA]1 with an excess of benzyl chloride leads to the formation of tetrabenzylphosphonium chloride, which was isolated in 61% yield. Sulfide 2 was used as a thionation reagent, converting benzophenone to thiobenzophenone in 62% yield. It also converted benzyl bromide to benzyl mercaptan in 55% yield. The TBA salt of trimetaphosphate ([TBA](3)[P3O9]center dot 2H(2)O), also a precursor to anion 1, was found to react with either trichlorosilane or silicon(IV) chloride to provide bis(trimetaphosphate)silicate, [TBA](2)[Si(P3O9)(2)], characterized by NMR spectroscopy, X-ray crystallography, and elemental analysis. Trichlorosilane reduction of [TBA](2)[Si(P3O9)(2)] also provided anion 1. The electronic structures of 1 and 2 were investigated using a suite of theoretical methods; the computational studies suggest that the trichlorosilyl ligand is a good pi-acceptor and forms sigma-bonds with a high degree of s character.
机译:用三氯硅烷还原磷酸(H3PO4)或四正丁基硫酸氢铵([TBA] [HSO4])导致形成双(三氯甲硅烷基)磷化物([P(SiCl3)(2)](-),1 )和三氯甲硅烷基硫化物([Cl3SiS](-),2)阴离子。阴离子1和2的TBA盐形成的平衡方程式是基于以下还原过程产生的副产物六氯二硅氧烷和氢气的确定:i)[H2PO4](-)+ 10HSiCl(3)-> 1 + P和ii)为4O(SiCl3)(2)+ 6H(2);对于S,[HSO4](-)+ 9HSiCl(3)-> 2 + 4O(SiCl3)(2)+ 5H(2)。通过随后使用Crabtree催化剂([(COD)Ir(py)-(PCy3)] [PF6],COD = 1,5-环辛二烯,py =吡啶,Cy =环己基)。磷酸1是通过磷酸与三氯硅烷的反应原位生成的,并用于将烷基氯(1-氯辛烷)转化为相应的伯膦,该伯膦的收率为41%。阴离子1也是由[TBA] [H2PO4]制备的,以克为单位分离,收率为62%。用过量的苄基氯处理[TBA] 1导致形成氯化四苄基phosph,其产率为61%。硫化物2用作硫磺化试剂,以62%的收率将二苯甲酮转化为硫代二苯甲酮。它还以55%的收率将苄基溴转化为苄基硫醇。三偏磷酸的TBA盐([TBA](3)[P3O9]中心点2H(2)O)也是阴离子1的前体,被发现与三氯硅烷或氯化硅(IV)反应生成双(三偏磷酸盐)硅酸盐[TBA](2)[Si(P3O9)(2)],其特征在于NMR光谱,X射线晶体学和元素分析。 [TBA](2)[Si(P3O9)(2)]的三氯硅烷还原也提供了阴离子1。使用一套理论方法研究了1和2的电子结构;计算研究表明,三氯甲硅烷基配体是一种良好的pi受体,并形成具有高度s特性的sigma键。

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