Hierarchical Superstructures by Combining Crystallization-Driven and Molecular Self-Assembly

被引:18
|
作者
Frank, Andreas [1 ,2 ]
Hils, Christian [3 ]
Weber, Melina [1 ,2 ]
Kreger, Klaus [1 ,2 ]
Schmalz, Holger [3 ]
Schmidt, Hansooo-Werner [1 ,2 ]
机构
[1] Univ Bayreuth, Macromol Chem 1, Univ Str 30, D-95447 Bayreuth, Germany
[2] Bavarian Polymer Inst, Univ Str 30, D-95447 Bayreuth, Germany
[3] Bavarian Polymer Inst, Keylab Synth & Mol Characterizat, Univ Str 30, D-95447 Bayreuth, Germany
关键词
crystallization-driven self-assembly; hierarchical superstructures; molecular self-assembly; patchy polymer fibers; supramolecular structures; SUPRAMOLECULAR POLYMERIZATION; CYLINDRICAL MICELLES; NANOPARTICLES; ARCHITECTURES; PATHWAY; LENGTH;
D O I
10.1002/anie.202105787
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combining the unique corona structure of worm-like patchy micelles immobilized on a polymer fiber with the molecular self-assembly of 1,3,5-benzenetricarboxamides (BTAs) leads to hierarchical superstructures with a fir-tree-like morphology. For this purpose, worm-like patchy micelles bearing pendant, functional tertiary amino groups in one of the corona patches were prepared by crystallization-driven self-assembly and immobilized on a supporting polystyrene fiber by coaxial electrospinning. The obtained patchy fibers were then immersed in an aqueous solution of a tertiary amino-functionalized BTA to induce patch-mediated molecular self-assembly to well-defined fir-tree-like superstructures upon solvent evaporation. Interestingly, defined superstructures are obtained only if the pendant functional groups in the surface patches match with the peripheral substituents of the BTA, which is attributed to a local increase in BTA concentration at the polymer fibers' surface.
引用
收藏
页码:21767 / 21771
页数:5
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