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Ion association and solvation behavior of tetraalkylammonium iodides in binary mixtures of dichloromethane + N,N-dimethylformamide probed by a conductometric study

机译:电导法研究四烷基碘化铵在二氯甲烷与N,N-二甲基甲酰胺的二元混合物中的离子缔合和溶剂化行为

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摘要

Precise measurements on electrical conductances of tetraalkylammonium iodides, R4NI (R = n-butyl to n-heptyl), in different mass% (0-100) of dichloromethane (DCM) + N,N-dimethylformamide (DMF) at 298.15 K have been performed. Limiting molar conductances (A_0), association constants (K_A) and co-sphere diameter (R) for ion-pair formation in the mixed solvent mixtures have been evaluated using the Fuoss conductance-concentration equation. However, the deviation of the conductometric curves (A versus √c) from linearity for the electrolytes in 100 mass% of DCM indicated triple ion formation, and therefore corresponding conductance data have been analyzed by the Fuoss-Kraus theory of triple ions. Limiting ionic molar conductances N have been calculated by the reference electrolyte method along with a numerical evaluation of ion pair and triple ion formation constants (K_P ≈ K_A and K_T). The results have been interpreted in terms of ion-solvent interactions and structural changes in the mixed solvents.
机译:在298.15 K的不同质量百分比(0-100)的二氯甲烷(DCM)+ N,N-二甲基甲酰胺(DMF)中,已精确测量了碘化四烷基铵碘化物R4NI(R =正丁基至正庚基)执行。已使用Fuoss电导浓度公式评估了混合溶剂混合物中离子对形成的极限摩尔电导(A_0),缔合常数(K_A)和共球直径(R)。然而,在100质量%DCM中,电解质的电导率曲线(A与√c)相对于线性的偏差表明形成了三重离子,因此已经通过Fuoss-Kraus三重离子理论分析了相应的电导数据。极限离子摩尔电导率N已通过参考电解质方法进行了计算,并对离子对和三重离子形成常数(K_P≈K_A和K_T)进行了数值评估。已根据离子-溶剂相互作用和混合溶剂中的结构变化来解释结果。

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