Single Chain Self-Assembly of Well-Defined Heterotelechelic Polymers Generated by ATRP and Click Chemistry Revisited

Single Chain Self-Assembly of Well-Defined Heterotelechelic Polymers Generated by ATRP and Click Chemistry Revisited
复制标题

DOI:
10.1002/pola.24688
复制
发表时间:
2011-06-15
影响因子:
--
通讯作者:
Barner-Kowollik, Christopher
Barner-Kowollik, Christopher
中科院分区:
化学3区
文献类型:
--
作者:
Altintas, Ozcan;Rudolph, Tobias;Barner-Kowollik, Christopher

文献摘要

被引文献

相似文献

携带胸腺嘧啶/二氨基吡啶(DAP)的明确杂遥爪聚苯乙烯(Mn,SEC 9300,PDI 1.04)和汉密尔顿楔形(HW)/氰尿酸(CA)(Mn,SEC 8200,PDI 1.04)键合基序通过受控/活性自由基聚合和铜催化的叠氮化物/炔“点击”化学的组合来制备,并且随后自组装为单链以模拟-在一个简单的水平上-天然生物大分子的自折叠行为。氘代二氯甲烷中的氢核磁共振(H-1 NMR)和动态光散射分析提供了胸腺嘧啶和ω-DAP以及杂遥爪聚合物的α-CA和ω-HW链端之间的氢键相互作用导致循环熵驱动的单链自组装的证据。本研究表明,NMR溶剂的选择是很重要的获得良好分辨的自组装结构的NMR谱。此外,对HW的空间效应可以影响自组装过程的效率。(C)2011 Wiley Periodicals,Inc.聚合物科学杂志A部分:聚合物化学49:2566-2576,2011
Well-defined heterotelechelic poly(styrene) carrying thymine/diaminopyridine (DAP) (Mn, SEC 9300, PDI 1.04) and Hamilton wedge (HW)/cyanuric acid (CA) (Mn, SEC 8200, PDI 1.04) bonding motifs are prepared via a combination of controlled/living radical polymerization and copper catalyzed azide/alkyne "click'' chemistry and are subsequently self-assembled as single chains to emulate-on a simple level-the self-folding behavior of natural biomacromolecules. Hydrogen nuclear magnetic resonance (H-1 NMR) in deuterated dichloromethane and dynamic light scattering analyses provides evidence for the hydrogen bonding interactions between the athymine and omega-DAP as well as alpha-CA and omega-HW chain ends of the heterotelechelic polymers leading to circular entropy driven single chain self-assembly. This study demonstrates that the choice of NMR solvent is important for obtaining well-resolved NMR spectra of the self-assembled structures. In addition, steric effects on the HW can affect the efficiency of the self-assembly process. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 2566-2576, 2011