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通过改变聚乙二醇端基的氢键能力来控制离子液体基双水相体系的形成

Controlling the Formation of Ionic-Liquid-based Aqueous Biphasic Systems by Changing the Hydrogen-Bonding Ability of Polyethylene Glycol End Groups.

作者信息

Pereira Jorge F B, Kurnia Kiki A, Freire Mara G, Coutinho João A P, Rogers Robin D

机构信息

Department of Chemistry, The University of Alabama, Tuscaloosa, AL 35487 (USA).

Department of Bioprocess and Biotechnology, School of Pharmacy, UNESP-São Paulo State University, 14801-902-Araraquara, SP (Brazil).

出版信息

Chemphyschem. 2015 Jul 20;16(10):2219-25. doi: 10.1002/cphc.201500146. Epub 2015 May 5.

Abstract

The formation of aqueous biphasic systems (ABS) when mixing aqueous solutions of polyethylene glycol (PEG) and an ionic liquid (IL) can be controlled by modifying the hydrogen-bond-donating/-accepting ability of the polymer end groups. It is shown that the miscibility/immiscibility in these systems stems from both the solvation of the ether groups in the oxygen chain and the ability of the PEG terminal groups to preferably hydrogen bond with water or the anion of the salt. The removal of even one hydrogen bond in PEG can noticeably affect the phase behavior, especially in the region of the phase diagram in which all the ethylene oxide (EO) units of the polymeric chain are completely solvated. In this region, removing or weakening the hydrogen-bond-donating ability of PEG results in greater immiscibility, and thus, in a higher ability to form ABS, as a result of the much weaker interactions between the IL anion and the PEG end groups.

摘要

通过改变聚合物端基的氢键供体/受体能力,可以控制聚乙二醇(PEG)水溶液与离子液体(IL)混合时双水相系统(ABS)的形成。结果表明,这些体系中的混溶/不混溶现象既源于氧链中醚基团的溶剂化作用,也源于PEG端基优先与水或盐的阴离子形成氢键的能力。PEG中哪怕去除一个氢键都会显著影响相行为,尤其是在聚合物链中所有环氧乙烷(EO)单元都完全溶剂化的相图区域。在该区域,去除或削弱PEG的氢键供体能力会导致更大的不混溶性,进而由于IL阴离子与PEG端基之间的相互作用弱得多,形成ABS的能力更高。

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本文引用的文献

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