标题: | 超分子聚合物的多重氢键诱导手性组态 Multiple Hydrogen-Bonded-Induced Chirality Organization in Supramolecular Polymers |
作者: | 谢宗益 朱超原 张丰志 应用化学系硕博士班 |
关键字: | 多重氢键;Multiple Hydrogen |
公开日期: | 2012 |
摘要: | 相较于传统的化学性聚合如自由基聚合、缩合聚合反应,近年来物理性聚合亦备受重视。本研究是设计一个简单的合成路径将聚丙二醇两端导入多点式氢键的官能基,在多点式互补氢键的驱使下产生自组装形成高分子的链段,并进行性质测定。同时,我们亦合成对照组,即导入不同超分子官能基,以便探讨此超分子官能基对各项物理性质的影响。 本文藉由1H-NMR、FT-IR鉴定其结构,证实(cy)2PPO、(ur-cy)2PPO及(cy-amide)2PPO成功被合成出来。并搭配DOSY核磁共振光谱分析,在浓度为0.3g/ml时,(ur-cy)2PPO重覆单元约为2500,说明此多点式互补氢键可自组装成高分子的链段,并进行一系列物理性质的鉴定。经由旋光度的测定发现(ur-cy)2PPO具有光学活性,证明了类螺旋结构。在应用端,由于1:32混掺锂盐比例可以成膜,故此超分子作用力改善材料的机械性质。 Compared to traditional chemical polymerization, such as radical polymerization, condensation polymerization, physical aggregation in recent years has also been taken seriously. This study is to design a simple synthetic pathway to import multi-point hydrogen bond functional groups at both ends of the polypropylene glycol, and self-assembly was driven to form the polymer chain segment by multiple complementary hydrogen bonding. We determine the product's physical properties. At the same time, we also synthesized the control group, that is to import different supramolecular functional groups, in order to explore the impact of different supramolecular functional groups on the various physical properties .By 1H-NMR, the FT-IR, structures were identified and confirmed (cy) 2PPO, (ur-cy) 2PPO and (cy-amide) 2PPO have been successfully synthesized. With DOSY NMR spectroscopy, in the concentration 0.3g/ml, (ur-cy) 2PPO repeat unit is about 2500, indicate that this multiple complementary hydrogen bonding indeed drive self-assembled into the polymer chain segments. Through optical rotation measurements ,we found (ur-cy)2PPO optically active, the evidence of a class of spiral structure. On the application side, due to the low molecular weight PPO monomer(with ratio polymer/lithium salt=32:1) can film ,therefore supramolecular interactions successfully improve the mechanical properties of the material. |
URI: | http://140.113.39.130/cdrfb3/record/nctu/#GT079925507 http://hdl.handle.net/11536/49845 |
显示于类别: | Thesis |