Lifshitz Yevgeniy, Golan Yuval, Konovalov Oleg, Berman Amir
Department of Materials Engineering, Ilse Katz Institute of Nanoscience and Nanotechnology, Beer-Sheva, Israel.
Langmuir. 2009 Apr 21;25(8):4469-77. doi: 10.1021/la8029038.
Polydiacetylene (PDA) Langmuir films (LFs) were investigated directly at the air/water interface using in situ synchrotron grazing incidence X-ray diffraction, and ex situ transmissison electron microscopy and diffraction. The films were compressed and polymerized on pure water. A crystallographic model describes the structures and phase transitions of the unpolymerized (monomer) film, via the metastable (blue phase), to the fully stable PDA red phase as a function of irradiation dose. The monomer-to-blue-to-red chromatic phase transitions are accompanied by changes in the in-plane crystal structure and pendant chains packing arrangement from arced alkyl chains (in the monomer and blue phases) to near-vertical closely packed chains in the red phase. Notably, the characteristic linear strand morphology of PDA films can be explained as a direct result of the marked decrease in spacing between adjacent polymer chains upon transition from the blue to the red phase.
利用原位同步加速器掠入射X射线衍射以及非原位透射电子显微镜和衍射技术,直接对聚二乙炔(PDA)朗缪尔膜(LFs)在空气/水界面进行了研究。这些膜在纯水上压缩并聚合。一个晶体学模型描述了未聚合(单体)膜的结构和相变,通过亚稳态(蓝相),随着辐照剂量的变化,转变为完全稳定的PDA红相。单体到蓝相再到红相的颜色相变伴随着面内晶体结构和侧链堆积排列的变化,从弧形烷基链(在单体和蓝相)转变为红相中近乎垂直紧密堆积的链。值得注意的是,PDA膜特有的线性链形态可以解释为从蓝相转变为红相时相邻聚合物链间距显著减小的直接结果。