Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks

被引:42
|
作者
Elacqua, Elizabeth [1 ,2 ]
Croom, Anna [1 ,2 ]
Manning, Kylie B. [1 ,2 ]
Pomarico, Scott K. [1 ,2 ]
Lye, Diane [1 ,2 ]
Young, Lauren [1 ,2 ]
Weck, Marcus [1 ,2 ]
机构
[1] NYU, Inst Mol Design, 100 Washington Sq East, New York, NY 10003 USA
[2] NYU, Dept Chem, 100 Washington Sq East, New York, NY 10003 USA
基金
美国国家科学基金会;
关键词
block copolymers; self-assembly; supramolecular chemistry; supramolecular polymers; OPENING METATHESIS POLYMERIZATION; SINGLE-CHAIN NANOPARTICLES; BETA-SHEET FOLDAMERS; POLYMERS; COMPLEXATION; FABRICATION; MOTIFS; WATER;
D O I
10.1002/anie.201609103
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report supramolecular AB diblock copolymers comprised of well-defined telechelic building blocks. Helical motifs, formed via reversible addition-fragmentation chain-transfer (RAFT) or anionic polymerization, are assembled with coil-forming and sheet-featuring blocks obtained via atom-transfer radical polymerization (ATRP) or ring-opening metathesis polymerization (ROMP). Interpolymer hydrogen bonding or metal-coordination achieves dynamic diblock architectures featuring hybrid topologies of coils, helices, and/or -stacked sheets that, on a basic level, mimic protein structural motifs in fully synthetic systems. The intrinsic properties of each block (e.g., circular dichroism and fluorescence) remain unaffected in the wake of self-assembly. This strategy to develop complex synthetic polymer scaffolds from functional building blocks is significant in a field striving to produce architectures reminiscent of biosynthesis, yet fully synthetic in nature. This is the first plug-and-play approach to fabricate hybrid -sheet/helix, -sheet/coil, and helix/coil architectures via directional self-assembly.
引用
收藏
页码:15873 / 15878
页数:6
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