首页> 外文期刊>Journal of the American Chemical Society >OXIDATIONS OF ER(3) (E=P, AS, OR SB) BY HYDROGEN PEROXIDE - METHYLRHENIUM TRIOXIDE AS CATALYST
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OXIDATIONS OF ER(3) (E=P, AS, OR SB) BY HYDROGEN PEROXIDE - METHYLRHENIUM TRIOXIDE AS CATALYST

机译:过氧化氢-三氧化二甲苯催化氧化ER(3)(E = P,AS或SB)

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Catalytic and noncatalytic conversions of tertiary phosphines to their oxides by hydrogen peroxide have been investigated. The catalyst is methylrhenium trioxide, CH3ReO3. The kinetics were investigated in acetonitrile-water (1:1 by volume) at 25 degrees C. Stepwise interactions between CH3ReO3 and H2O2 form CH3Re(eta(2)-O-2)(O)(2)(OH2), A, and CH3Re(eta(2)-O-2)(2)(O)(OH2), B. In CH3CN-H2O ( 1:1 v/v) the equilibrium constants are K-1 = 13 +/- 2 L mol(-1) and K-2 = 136 +/- 28 L mol(-1) at pH 1.0 and 25 degrees C. The forward and reverse rate constants for the formation of A in this medium are k(1) = 32.5 +/- 0.3 L mol(-1) s(-1) and k(-1) = 3.0 +/- 0.2 s(-1). Systematic changes in the substituents on phosphorus were made to vary the nucleophilicity of the phosphine and its cone angles; the kinetic effects are discernible, although they Lie in a narrow range. Triphenylarsine and triphenylstibine were also studied, and their rates are within a factor of 2 of that for PPh(3). The rhenium peroxides A and B show a small difference in reactivity. The bimolecular reactions between A and most of the phosphines have rate constants of the order 10(5) L mol(-1) s(-1). The kinetic data support a mechanism that allows nucleophilic attack of the substrate at the rhenium peroxides. [References: 39]
机译:已经研究过氧化氢将叔膦催化和非催化转化为氧化物。催化剂是三氧化二甲基methyl CH3ReO3。在乙腈-水(体积比为1:1)中于25摄氏度下研究了动力学。CH3ReO3和H2O2之间的逐步相互作用形成CH3Re(eta(2)-O-2)(O)(2)(OH2),A,和CH3Re(eta(2)-O-2)(2)(O)(OH2),B。在CH3CN-H2O(1:1 v / v)中,平衡常数为K-1 = 13 +/- 2 L mol(-1)和K-2 =在pH 1.0和25摄氏度下136 +/- 28 L mol(-1)。在这种介质中形成A的正向和反向速率常数为k(1)= 32.5 +/- 0.3 L mol(-1)s(-1)和k(-1)= 3.0 +/- 0.2 s(-1)。对磷上的取代基进行了系统的改变,以改变膦的亲核性及其锥角。虽然它们的作用范围很窄,但它们的动力学作用是可以看出的。还研究了三苯ar和三苯他滨,它们的发生率在PPh(3)的2倍之内。过氧化rhA和B的反应性差异很小。 A和大多数膦之间的双分子反应的速率常数约为10(5)L mol(-1)s(-1)。动力学数据支持一种机制,该机制允许底物在过氧化rh下发生亲核攻击。 [参考:39]

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