Judd Kenneth D, Mendes de Oliveira Denilson, Urbina Andres S, Ben-Amotz Dor
Department of Chemistry, Purdue University West Lafayette IN 47907 USA
Chem Sci. 2024 Apr 3;15(17):6378-6384. doi: 10.1039/d3sc06995h. eCollection 2024 May 1.
In spite of the ubiquity of acid/base ions and salts in biological systems, their influence on hydrophobic self-assembly remains an open question. Here we use a combined experimental and theoretical strategy to quantify the influence of H and OH, as well as salts containing Li, Na, Cl and Br, on the hydrophobic self-assembly of micelles composed of neutral oily 1,2-hexanediol surfactants. The distributions of aggregate sizes, both below and above the critical micelle concentration (CMC), are determined using Raman multivariate curve resolution (Raman-MCR) spectroscopy to quantify the multi-aggregation chemical potential surface (MCPS) that drives self-assembly. The results reveal that ions have little influence on the formation of hydrophobic contact dimers but can significantly drive high-order self assembly. Moreover, the hydration-shells of oily solutes are found to expel the above salt ions and OH, but to attract H, with wide-ranging implications.
尽管酸碱离子和盐在生物系统中无处不在,但它们对疏水自组装的影响仍是一个悬而未决的问题。在这里,我们采用实验与理论相结合的策略,来量化H和OH以及含Li、Na、Cl和Br的盐对由中性油性1,2 -己二醇表面活性剂组成的胶束的疏水自组装的影响。使用拉曼多元曲线分辨(Raman - MCR)光谱法测定临界胶束浓度(CMC)上下的聚集体尺寸分布,以量化驱动自组装的多聚集体化学势表面(MCPS)。结果表明,离子对疏水接触二聚体的形成影响不大,但能显著驱动高阶自组装。此外,发现油性溶质的水合壳会排斥上述盐离子和OH,但会吸引H,这具有广泛的影响。