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Rate and Product Studies of 5-Dimethylamino-Naphthalene-1-Sulfonyl Chloride under Solvolytic Conditions

机译:溶剂化条件下5-二甲基氨基萘-1-磺酰氯的合成速率及产物研究

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摘要

The solvolysis rate constants of 5-dimethylamino-naphthalene-1-sulfonyl chloride ((CH3)2NC10H6SO2Cl, 1) in 31 different solvents are well correlated with the extended Grunwald-Winstein equation, using the NT solvent nucleophilicity scale and YCl solvent ionizing scale with sensitivity values of 0.96 ± 0.09 and 0.53 ± 0.03 for l and m, respectively; the correlation coefficient value was 0.955. These l and m values can be considered to support an SN2 reaction pathway having a transition state (TS) structure similar to that of the benzenesulfonyl chloride reaction. This interpretation is further supported by the activation parameters, i.e., relatively small positive ΔH≠ (12.0 to 15.9 kcal·mol−1) and large negative ΔS≠ (−23.1 to −36.3 cal·mol−1·K−1) values, and the solvent kinetic isotope effects (SKIEs, 1.34 to 1.88). Also, the selectivity values (S = 1.2 to 2.9) obtained in binary solvents are consistent with the proposed mechanism.
机译:使用NT溶剂亲核标度和YCl溶剂电离标度,在31种不同溶剂中的5-二甲基氨基萘-1-磺酰氯((CH3)2NC10H6SO2Cl,1)的溶剂分解速率常数与扩展Grunwald-Winstein方程良好相关。 l和m的灵敏度分别为0.96±0.09和0.53±0.03;相关系数值为0.955。可以认为这些l和m值支持具有类似于苯磺酰氯反应的过渡态(TS)结构的SN2反应途径。激活参数,即相对较小的正ΔH≠(12.0至15.9 kcal·mol-1)和较大的负ΔS≠(-23.1至-36.3 cal·mol-1·K-1)值进一步支持了这种解释,以及溶剂动力学同位素效应(SKIE,1.34至1.88)。同样,在二元溶剂中获得的选择性值(S = 1.2至2.9)与所提出的机理一致。

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