Frauenrath Holger, Jahnke Eike
ETH Zürich, Department of Materials, Wolfgang-Pauli-Strasse 10, HCI H515, 8093 Zürich, Schweiz.
Chemistry. 2008;14(10):2942-55. doi: 10.1002/chem.200701325.
Typical biopolymers exhibit structures and order on different length scales. By contrast, the number of synthetic polymers with a similar degree of hierarchical structure formation is still limited. Starting from recent investigations on the structures of amyloid proteins as well as research activities toward nanoscopic scaffolds from synthetic oligopeptides and their polymer conjugates, a general strategy toward hierarchically structured pi-conjugated polymers can be developed. The approach relies on the supramolecular self-assembly of diacetylene macromonomers based on beta-sheet forming oligopeptides equipped with hydrophobic polymer segments. Polymerization of these macromonomers proceeds under retention of the previously assembled hierarchical structure and yields pi-conjugated polymers with multi-stranded, multiple-helical quaternary structures.
典型的生物聚合物在不同长度尺度上呈现出结构和有序性。相比之下,具有相似层次结构形成程度的合成聚合物数量仍然有限。从最近对淀粉样蛋白结构的研究以及合成寡肽及其聚合物缀合物用于纳米级支架的研究活动出发,可以开发出一种构建层次结构π共轭聚合物的通用策略。该方法依赖于基于配备疏水聚合物链段的β-折叠形成寡肽的二乙炔大分子单体的超分子自组装。这些大分子单体的聚合在保留先前组装的层次结构的情况下进行,并产生具有多链、多螺旋四级结构的π共轭聚合物。