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Equilibrium Ion Pair Acidities of Polyhalogenated Benzenes in THF. Extrapolation to Benzene

机译:多卤代苯在THF中的平衡离子对酸度。外推到苯

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The equilibrium cesium ion pair acidities of six polyfluorobenzenes at 25 ℃ and six polychloroben-zenes at -20 ℃ were determined in THF. For fluorinated benzenes the additive (negative) effects of fluorine on pK (partial equilibrium factors) are o = 5.2, m = 3.0, and p = 1.4. From these the cesium ion pair pK (per H) of benzene is extrapolated to be 44.8 at 25 ℃. For chlorobenzenes the additive contributions for o-, m-, and p-chlorine are 4.2,2.7, and 2.1, respectively. The corresponding pK of benzene is 47.0 at -20 ℃. Aggregation studies show that in the concentration range 10~(-3)-10~(-4) M the cesium salt of 1,2,4,5-tetrachlorobenzene and the cesium and lithium salts of 1,2,4,5-tetrafluorobenzene are monomeric. The pK of benzene on the Li scale is extrapolated to be 39.5.
机译:在THF中测定了25℃下的6个多氟苯和-20℃下的6个多氯苯-Zenes的平衡铯离子对酸度。对于氟化苯,氟对pK(部分平衡因子)的累加(负)效应为o = 5.2,m = 3.0和p = 1.4。从这些推断出,铯的铯离子对pK(每H)在25℃下推断为44.8。对于氯苯,邻氯,间氯和对氯的添加剂贡献分别为4.2、2.7和2.1。 -20℃下苯的相应pK为47.0。聚集研究表明,浓度范围为10〜(-3)-10〜(-4)M的1,2,4,5-四氯苯铯盐和1,2,4,5-铯和锂盐四氟苯是单体。 Li级的苯的pK推断为39.5。

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