Lee Su Rim, Yoon Dong Ki, Park Sang-Hyun, Lee Eun Ho, Kim Yun Ho, Stenger Patrick, Zasadzinski Joseph A, Jung Hee-Tae
Department of Chemical & Biomolecular Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong, Yuseong-gu, Daejeon 305-701 Korea.
Langmuir. 2005 May 24;21(11):4989-95. doi: 10.1021/la050487v.
We have investigated the surface ordering of a synthetic, asymmetric, fan-shaped dendrimer containing a carboxyl core and perfluorinated tails which was obtained by the esterification of the intermediary. X-ray diffraction patterns and transmission electron microscopy (TEM) images show the molecules self-assemble into a hexagonal, cylindrical mesophase. Surface pressure-area isotherms and Brewster angle microscopy measurements show the molecule forms a stable monolayer at the air-water interface with a single phase transition. As a condensed monolayer, the perfluorinated tails are well-packed with hexagonal symmetry with (10) spacing of approximately 0.5 nm from molecular-scale atomic force microscopy (AFM) images. Such dense molecular-scale packing has not been observed in other dendritic molecules thus far. Compared to the case of conventional dendritic molecules with alkyl tails, these molecules occupy a much smaller molecular area due to the strong microphase separation between the carboxylic core and perfluorinated tails at the air-water interface. After monolayer collapse, the irregular islands with terrace morphology are observed in contrast with conventional alkyl-terminated self-assembled dendritic molecules where irregular islands do not appear. The interfacial and internal structure of every terrace shows planar columnar morphology from AFM and TEM imaging. From these results, we discuss the stability of perfluorinated, self-assembled dendrimers on water, as well as how to generate planar morphology on a hydrophilic surface.
我们研究了一种合成的、不对称的、扇形树枝状大分子的表面有序性,该树枝状大分子含有羧基核心和全氟尾链,是通过中间体的酯化反应得到的。X射线衍射图谱和透射电子显微镜(TEM)图像表明,这些分子自组装成六方柱状中间相。表面压力-面积等温线和布鲁斯特角显微镜测量表明,该分子在气-水界面形成稳定的单分子层,且有单一的相变。作为凝聚单分子层,从分子尺度的原子力显微镜(AFM)图像可知,全氟尾链以六方对称紧密堆积,(10)间距约为0.5 nm。迄今为止,在其他树枝状分子中尚未观察到这种密集的分子尺度堆积。与具有烷基尾链的传统树枝状分子相比,由于在气-水界面处羧基核心和全氟尾链之间存在强烈的微相分离,这些分子占据的分子面积要小得多。单分子层坍塌后,观察到具有梯田形态的不规则岛状结构,这与传统的烷基封端自组装树枝状分子不同,后者不会出现不规则岛状结构。从AFM和TEM成像可以看出,每个梯田的界面和内部结构均呈现平面柱状形态。基于这些结果,我们讨论了全氟自组装树枝状大分子在水上的稳定性,以及如何在亲水性表面上生成平面形态。