Morphological characterization of the molecular superstructure of polyphenylene ethynylene derivatives

被引:36
作者
Schnablegger, H
Antonietti, M
Göltner, C
Hartmann, J
Cölfen, H
Samorí, P
Rabe, JP
Häger, H
Heitz, W
机构
[1] Max Planck Inst Kolloid & Grenzflachenforsch, D-14513 Teltow, Germany
[2] Humboldt Univ, Inst Phys Makromol, D-10115 Berlin, Germany
[3] Univ Marburg, Fachbereich Phys Chem, D-35032 Marburg, Germany
关键词
polyphenylene ethynylene; aggregation; superstructure; main-chain stiff polymers;
D O I
10.1006/jcis.1998.5970
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two different polyphenylene ethynylene derivatives, one partly hydrophobic and one hydrophilic, were investigated with a combination of X-lay and light scattering techniques and hydrodynamic techniques, as well as scanning force microscopy and transmission electron microscopy to elucidate their molecular structure and aggregation behavior in tetrahydrofuran and water, respectively. It turns out that both polymers possess a rod-like molecular architecture which, however, is the basis of a cascade of aggregation steps. Both, electron microscopy and X-ray analysis support the concept of a primary back-to-back aggregation of polymer chains into cylindrically shaped aggregates with high anisometry. The thickness of these aggregates was between 4.0 and 4.5 nn. The aggregates of the hydrophobic polymer further associate into fibrils and these fibrils form clusters of globular shape, though with high internal anisometry. (C) 1999 Academic Press.
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页码:24 / 32
页数:9
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