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由烯基琥珀酸酯封端的双极性两亲分子制备用于大规模应用的有序液体和水凝胶。

Ordered liquids and hydrogels from alkenyl succinic ester terminated bola-amphiphiles for large-scale applications.

作者信息

Lohmeier Thomas, Bredol Michael, Schreiner Eduard, Hintze-Bruening Horst

机构信息

BASF Coatings GmbH, Glasuritstrasse 1, 48165 Muenster, Germany.

出版信息

Soft Matter. 2014 Sep 7;10(33):6237-48. doi: 10.1039/c4sm01102c.

Abstract

The present study describes an economic and scalable approach to aqueous mesophases from bola-amphiphiles (BA) obtained via nucleophilic addition of dimer fatty acid based α,ω-polyesterdiols (PES) on cyclic acid anhydrides and conversion of the carboxylic end groups into ammonium salts. Novel bola-amphiphilic head groups are introduced using alkenyl succinic anhydrides (ASA). The additional terminal hydrophobic side chains favour the self-assembly of polymeric BA of different molecular weights into nanoscale anisotropic objects, their shape and ordering into nematic or lamellar-like phases being dependent on the length and structural uniformity of the ASA chains. Corresponding diester based on C15 (hydrogenated bisphenol-A, HBA) and C8 (1,4-cyclohexanedimethanol, CHDM) spacers have been prepared and the self-assembly of the resulting BA in water has been studied using SAXS, (2)H-NMR and optical polarization microscopy. While the rigid C8 spacer impedes any ordering, ASA capped C15 tends to form ordered hydrogels over extended regions of the phase diagram that resemble mesh phases and L(α)/L(3) polymorphism. Rheological and simulation results confirm the presence of elastically responding bicontinuous morphologies and biased porous assemblies resembling interconnected mesh phases. Both the use of the dimer fatty acid based spacer as well as of ASA head groups open up large-scale applications of ordered liquids (or hydrogels) as a formulation basis for e.g. films, coatings and adhesives.

摘要

本研究描述了一种经济且可扩展的方法,用于从通过基于二聚脂肪酸的α,ω - 聚酯二醇(PES)与环状酸酐进行亲核加成,并将羧基端基转化为铵盐而获得的双 bola 两亲分子(BA)制备水性中间相。使用烯基琥珀酸酐(ASA)引入新型双 bola 两亲头基。额外的末端疏水侧链有利于不同分子量的聚合物 BA 自组装成纳米级各向异性物体,其形状以及向向列相或层状相的有序排列取决于 ASA 链的长度和结构均匀性。基于 C15(氢化双酚 A,HBA)和 C8(1,4 - 环己烷二甲醇,CHDM)间隔基的相应二酯已被制备,并使用小角 X 射线散射(SAXS)、氘核磁共振(²H - NMR)和光学偏振显微镜研究了所得 BA 在水中的自组装。虽然刚性的 C8 间隔基阻碍任何有序排列,但 ASA 封端的 C15 在相图的扩展区域倾向于形成类似于网状相和 L(α)/L(3)多晶型的有序水凝胶。流变学和模拟结果证实了存在具有弹性响应的双连续形态以及类似于相互连接的网状相的有偏多孔组装体。基于二聚脂肪酸的间隔基以及 ASA 头基的使用都为有序液体(或水凝胶)作为例如薄膜、涂料和粘合剂的配方基础开辟了大规模应用。

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