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首页> 外文期刊>Journal of the American Chemical Society >LIFETIMES OF IMINIUM IONS IN AQUEOUS SOLUTION
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LIFETIMES OF IMINIUM IONS IN AQUEOUS SOLUTION

机译:水溶液中次离子的寿命

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Iminium cations have been generated in aqueous solution from the solvolysis of anilinothioethers ArN(CH3)CH(2)SR at 25 degrees C. Common ion inhibition of the solvolysis of anilinothioethers was observed when the thiolate anion leaving group was added to the reaction mixture. This inhibition results from trapping of the iminium ion by RS(-) to regenerate the anilinothioether. Rate constants, k(H2O), for hydration of the iminium ions were determined from common ion inhibition of the solvolysis of anilinothioethers in the presence of added thiolate ions and a rate constant of 5 x 10(9) M(-1) s(-1) for diffusion-controlled trapping of the iminium ions by RS(-), which regenerates the starting material. The values of k(H2O) for H2C=N+(CH3)C(6)H(4)X are 1.0 x 10(8), 3.1 x 10(7), 3.0 x 10(7), 5.5 x 10(6), 4.5 x 10(6), and 3.1 x 10(6) s(-1) for X = 4-NO2, 4-CN, 3-NO2, 3-Cl, 4-COO-, and 4-Cl, respectively. Rate constants for the solvolysis of anilinothioethers, k(solv) depend on the pK(a) of the thiolate leaving group with beta(1g) = -0.93 +/- 0.09, which shows that the dissociation reaction has a very late transition state. This result is consistent with rate-limiting diffusion-controlled encounter of RS(-) with H2C=N+(CH3)Ar in the reverse direction. The value of beta(nuc) = 1.00-0.93 = 0.07 +/- 0.09 approximate to 0 is expected for a diffusion-controlled addition reaction. The solvolysis reaction is sensitive to the basicity of the electron-donating nitrogen atom of the aniline with a value of beta(dg) = 0.79 +/- 0.06; i.e., there is a large amount of electron donation from the nitrogen atom that provides the driving force for cleavage of the CH2-S bond in the late transition state. Hammett correlations of the rate constants for the solvolysis reaction, k(solv), show a better correlation with sigma(-) than with sigma for substituents on the aniline and follow rho(-) = -3.3 +/- 0.3. This also indicates a large amount of electron donation and an important contribution of resonance in the transition state of the solvolysis reaction. Reaction of the iminium ions with water is accelerated by electron-withdrawing substituents on the aniline ring and follows rho(-) = 1.5 +/- 0.2 and beta(dg) = -0.35 +/- 0.03; i.e., the rate of reaction of the iminium cation with water is approximately half as sensitive to polar substituents as the solvolysis reaction. [References: 30]
机译:在25摄氏度下,苯硫基硫醚ArN(CH3)CH(2)SR的溶剂化已在水溶液中产生亚胺阳离子。当将硫醇盐阴离子离去基团添加到反应混合物中时,观察到苯胺基硫醚的溶剂化的常见离子抑制作用。这种抑制作用是由于RS(-)捕获亚胺离子以再生苯胺基硫醚。在添加的硫醇盐离子存在下,苯胺硫醚的溶剂分解过程中常见的离子抑制作用和5 x 10(9)M(-1)s(的速率常数)的常数离子抑制作用确定了亚胺离子水合的速率常数k(H2O)。 -1)用于通过RS(-)进行扩散控制的亚胺离子的捕集,从而使原料再生。 H2C = N +(CH3)C(6)H(4)X的k(H2O)值为1.0 x 10(8),3.1 x 10(7),3.0 x 10(7),5.5 x 10(6) ),X = 4-NO2、4-CN,3-NO2、3-Cl,4-COO-和4-Cl的4.5 x 10(6)和3.1 x 10(6)s(-1),分别。苯硫基硫醚的溶剂分解速率常数k(solv)取决于硫醇盐离去基团的pK(a),β(1g)= -0.93 +/- 0.09,这表明解离反应的过渡态非常晚。该结果与RS(-)在H2C = N +(CH3)Ar的反方向上的限速扩散控制相遇一致。对于扩散控制的加成反应,期望β(nuc)= 1.00-0.93 = 0.07 +/- 0.09的值接近0。溶剂分解反应对苯胺的供电子氮原子的碱度敏感,β(dg)= 0.79 +/- 0.06;即,来自氮原子的大量电子给体提供了驱动力,用于在后期转变状态下裂解CH2-S键。溶剂分解反应速率常数k(solv)的Hammett相关性显示,与sigma(-)的相关性比与sigma(-)的苯胺取代基相关性更好,并且遵循rho(-)= -3.3 +/- 0.3。这也表明在溶剂分解反应的过渡态中大量的电子给予和共振的重要贡献。亚胺离子与水的反应通过苯胺环上的吸电子取代基而加速,并遵循rho-(-)= 1.5 +/- 0.2和beta(dg)= -0.35 +/- 0.03;即,亚胺阳离子与水的反应速率对极性取代基的敏感度约为溶剂分解反应的一半。 [参考:30]

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