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Thermodynamic Protonation Parameters of some Sulfur-Containing Anions in NaClaq and (CH3)(4)NClaq at t=25 degrees C

机译:NaClaq和(CH3)(4)NClaq中t = 25时某些含硫阴离子的热力学质子化参数

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摘要

Protonation constants of one thiocarboxylate (thioacetate) and four sulfur-containing carboxylates (2-methylthioacetate, thiolactate, thiomalate, 3-mercaptopropionate) were determined by potentiometric measurements in a wide ionic strength range [0 <= I <= 5 mol.L-1 in NaCl and 0 <= I <= 3 mol.L-1 in (CH3)(4)NCl] at t = 25 degrees C. For two of these ligands (2-methylthioacetate and thiolactate), the protonation enthalpies were also determined by calorimetric measurements in NaCl ionic medium [0 <= I <= 5 mol.L-1] at t = 25 degrees C. Individual UV spectra of the protonated and unprotonated 3-mercaptopropionate species, together with values of the protonation constants, were obtained by spectrophotometric titrations. Results were analyzed in terms of their dependence on the ionic medium by using different thermodynamic models [Debye-Huckel type, SIT (Specific ion Interaction Theory) and Pitzer's equations]. Differences among protonation constants obtained in different media were also interpreted in terms of weak complex formation.
机译:通过电位测量在较宽的离子强度范围内[0 <= I <= 5 mol.L-在t = 25℃时在NaCl中为1,在(CH3)(4)NCl]中为0 <= I <= 3 mol.L-1。对于这些配体中的两个(2-甲基硫代乙酸酯和巯基乳酸),质子化焓也为通过在t = 25℃下在NaCl离子介质[0 <= I <= 5 mol.L-1]中进行量热法测定。质子化和未质子化的3-巯基丙酸酯物种的各个UV光谱,以及质子化常数的值,通过分光光度滴定法获得。通过使用不同的热力学模型[Debye-Huckel类型,SIT(特定离子相互作用理论)和Pitzer方程],分析了结果对离子介质的依赖性。还根据弱复合物的形成来解释在不同介质中获得的质子化常数之间的差异。

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