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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:通过三氯硅烷基和硫化物阴离子,对磷酸酯(E = P,S)键形成的正正磷酸盐和硫酸盐利用

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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:用三氯硅烷的磷酸(H3PO4)或磷酸(H3PO4)或磷酸二丁基铵([TBA] [HSO4])导致BIS(三氯硅烷基)磷化物的形成([P(SiCl3)(2)]( - ),1 )分别分别和三氯硅烷硫醚([Cl 3SIS]( - ),2)个阴离子。为形成阴离子1和2的TBA盐的平衡方程,基于六氯二硅氧烷和氢气作为由这些还原过程产生的副产物的鉴定:I)[H2PO4]( - )+ 10HSICL(3) - > 1 +对于P和II)的4O(SiCl 3)(2)+ 6H(2))[HSO4]( - )+ 9HSICL(3) - > 2 + 40(SiCl 3)(2)+ 5H(2)用于S.氢气通过其随后用来使用Crabtree的催化剂氢化烯烃(( - ) - 萜烯-4-醇)([(鳕鱼)IR(py) - (pcy3)] [PF6],COD = 1,5-环辛二烯,PY =吡啶,Cy =环己基)。通过磷酸和三氯硅烷的反应原位产生磷化膦1,并用于将烷基氯(1-氯辛烷)转化为相应的一次膦,其分离为41%的产率。阴离子1也由[TBA] [H2PO4]制备,并在克尺度上分离62%的产率。过量苄基氯化苄基的[TBA] 1的处理导致四苄基氯化鏻的形成,其分离为61%的产率。硫化物2用作归剂试剂,将二苯甲酮转化为硫代苯酮,产率62%。它还将苄基溴化物转化为55%收率的苄硫醇。发现三磷酸盐的TBA盐([TBA](3)[P3O9]中心点2h(2)),也发现阴离子1的前体与三氯硅烷或硅(IV)氯化物反应,以提供双(三磷酸盐)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良好的PI-acceptor,并具有高度的S特征的σ键。

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