化学
等温滴定量热法
乙腈
水溶液
反离子
两亲性
焓
量热法
胶束
物理化学
热力学
有机化学
聚合物
离子
共聚物
物理
作者
Roberto Fernandez‐Alvarez,Žiga Medoš,Zdeněk Tošner,Alexander Zhigunov,Mariusz Uchman,Stefan Hervø-Hansen,Mikael Lund,Marija Bešter‐Rogač,Pavel Matějíček
出处
期刊:Langmuir
[American Chemical Society]
日期:2018-10-21
卷期号:34 (47): 14448-14457
被引量:18
标识
DOI:10.1021/acs.langmuir.8b03462
摘要
Isothermal titration calorimetry (ITC) is an apt tool for a total thermodynamic description of self-assembly of atypical amphiphiles such as anionic boron cluster compounds (COSAN) in water. Global fitting of ITC enthalpograms reveals remarkable features that differentiate COSAN from classical amphiphiles: (i) strong enthalpy and weak entropy contribution to the free energy of aggregation, (ii) low degree of counterion binding, and (iii) very low aggregation number, leading to deviations from the ideal closed association model. The counterion condensation obtained from the thermodynamic model was compared with the results of 7Li DOSY NMR of Li[COSAN] micelles, which allows direct tracking of Li cations. The basic thermodynamic study of COSAN alkaline salt aggregation was complemented by NMR and ITC experiments in dilute Li/NaCl and acetonitrile aqueous solutions of COSAN. The strong affinity of acetonitrile molecules to COSAN clusters was microscopically investigated by all-atomic molecular dynamics simulations. The impact of ionic strength on COSAN self-assembling was comparable to the behavior of classical amphiphiles, whereas even a small amount of acetonitrile cosolvent has a pronounced nonclassical character of COSAN aggregation. It demonstrates that large self-assembling changes are triggered by traces of organic solvents.
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