化学
电位滴定法
水溶液
滴定法
离子强度
遗传算法
无机化学
配体(生物化学)
离子键合
药物化学
离子
物理化学
有机化学
生物
生物化学
受体
进化生物学
作者
Anna Irto,Ileana Ielo,Clemente Bretti,Francesco Crea,Concetta De Stefano,Rosalia Maria Cigala
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-07-16
卷期号:30 (14): 2991-2991
标识
DOI:10.3390/molecules30142991
摘要
The interactions of Fe3+ with some ligands (Tranexamic (TXA−), Indole-3-acetic (IAA−), and Aminomethylphosphonic (AMPA2−) acids) of biological and environmental interest were studied. The speciation studies were performed in NaNO3(aq) and NaCl(aq) using potentiometric and, only for IAA−, spectrophotometric titrations at T = 298.15 K and 0.01 ≤ I/mol dm−3 ≤ 1.0. The proposed speciation models are as follows: Fe(TXA)H3+, Fe(TXA)2+, Fe(TXA)(OH)+, and Fe(TXA)(OH)2(aq) for TXA−; Fe(IAA)2+ for IAA−; and Fe(AMPA)H23+, Fe(AMPA)H2+, and Fe(AMPA)+ for AMPA2−. A comparison of logβ for the common FeL species gives logβFeIAA = 6.56 and logβFeAMPA = 14.84 (at I = 1.00 mol dm−3 and T = 298.15 K), suggesting that AMPA2− has a higher complexing ability towards Fe3+ than IAA−. The dependence on the ionic strength of the formation constants was modeled by means of a Debye–Hückel type equation and the SIT model, whilst the sequestering ability of the investigated ligands towards Fe3+ was quantified at various pHs, ionic strengths, and in the different supporting electrolytes by means of an empirical pL0.5 parameter. To complete this study of the behavior of the different Fe3+/ligand systems, various simulations in biological fluids and natural waters were conducted.
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