糖基、肽基和核碱基亲水分子形成高轴比微结构

T. Shimizu
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引用次数: 1

摘要

合成了多种由糖、肽或核碱基连接到碳氢化合物间隔基团两端的双氧水型两亲体(bolaamphiphiles)。这些化合物在水溶液中自组装形成热稳定的纳米级高轴向比微结构(HARMs),如螺旋纤维、管状纤维和双螺旋绳。结构的大小分布与自组装纤维结构(如胶原纤维、鞭毛和肌动蛋白纤维)基本相同,并且发现形态强烈依赖于所使用的低聚亚甲基间隔物的链长和奇碳数。利用FT-IR、XRD和AFM等手段研究了哈姆斯的分子排列和氢键网络。单层纤维的层间和层内相互作用被认为是纤维形态的主要决定因素。危害是以类似于生物结构的方式分层构建的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation of High-Axial-Ratio Microstructures from Sugar-, Peptide-, and Nucleobase-based Bolaamphiphiles
A variety of bola-form amphiphiles (bolaamphiphiles), in which sugar, peptide, or nucleobase moieties are connected to both ends of a hydrocarbon spacer, were synthesized. These compounds self-assembled in aqueous solution to form thermally stable, nanometer-scale high-axial-ratio microstructures (HARMs), such as helical fibers, tubular fibers, and double-helical ropes. Size distribution of the structures was essentially the same as that of self-assembled fibrous structures like collagen fibers, flagella, and actin fibers and morphology was found to strongly depend on chain length and even-odd carbon number of used oligomethylene spacers. Molecular arrangement and hydrogen bond networks within HARMs were investigated by FT-IR, XRD, and AFM. Interlayer and intralayer interactions of the monolayers were noted to be major determinants of fiber morphology. HARMs are constructed hierarchically in a manner similar to biological structures.
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