聚合物
图像拼接
双层
分子
材料科学
立体中心
分散性
化学物理
结晶学
化学
高分子化学
膜
有机化学
生物化学
对映选择合成
人工智能
复合材料
催化作用
计算机科学
作者
Samuel I. Stupp,Seung-Rak Son,Hsin‐Chieh Lin,L. S. Li
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1993-01-01
卷期号:259 (5091): 59-63
被引量:225
标识
DOI:10.1126/science.259.5091.59
摘要
A synthetic pathway is described to construct "in bulk" two-dimensional (2D) polymers shaped as molecular sheets. A chiral oligomeric precursor is used that contains two reactive sites, a polymerizable group at one terminus and a reactive stereogenic center near the middle of the molecule. The bulk reaction yields bilayer 2D polymers of molecular weight in the order of millions and a monodisperse thickness of 50.2 angstroms. The 2D molecular objects form through molecular recognition by the oligomers, which self-organize into layers that place the reactive groups within specific planes. The oligomers become catenated by two different stitching reactions involving the reactive sites. At room temperature, stacks of these molecular objects can organize as single crystals and at higher temperatures melt into smectic liquid crystals. Nonlinear optical experiments reveal that solid films containing the 2D polymers form structures that are thermally and temporally more stable than those containing analogous 1D polymers. This observation suggests that the transformation of common polymers from a 1D to a 2D architecture may produce generations of organic materials with improved properties.
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