ΔG° and TΔS° charge relationships for the binding of carboxylic anions by open-chain polyammoninm cations

被引:19
作者
De Stefano, C [1 ]
Giuffre, O [1 ]
Sammartano, S [1 ]
机构
[1] Univ Messina, Dipartimento Chim Inorgan Chim Analit & Chim Fis, I-98166 Messina, Vill S Agata, Italy
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1998年 / 94卷 / 16期
关键词
D O I
10.1039/a804169e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Enthalpies of formation have been determined by titration calorimetry for complexes formed by some polycarboxylic anions (citrate, 1,2,3-propanetricarboxylate, 1,2,3,4-butanetetracarboxylate) with open-chain polyammonium cations C2(n-1)NnH(6n-2)(n+) (n = 2-6), at 25 degrees C. Delta H degrees values are generally positive and, therefore, these complexes are entropically stabilized. Delta G degrees and T Delta S degrees follow a linear trend as a function of polyammonium cation and carboxylic anion charges. The linear dependence on charges of Delta G degrees is the same for different systems, whilst that of T Delta S degrees is specific for each system. Delta G degrees and T Delta S degrees charge relationships are reported.
引用
收藏
页码:2395 / 2398
页数:4
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