Highly regular organization of conjugated polymer chains via block copolymer self-assembly

被引：0
|
作者：
Leclère, P
Calderone, A
Marsitzky, D
Francke, V
Geerts, Y
Müllen, K
Brédas, JL
Lazzaroni, R
机构：
[1] Univ Mons, Ctr Rech Elect & Photon Mol, Serv Chim Mat Nouveaux, B-7000 Mons, Belgium
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
来源：
ADVANCED MATERIALS | 2000年 / 12卷 / 14期
关键词：
D O I：
10.1002/1521-4095(200007)12:14<1042::AID-ADMA1042>3.0.CO;2-J
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The microscopic organization in thin films of block copolymers containing either polyparaphenylene, or polyphenyleneethynylene rigid segments covalently bound to a flexible polydimethylsiloxane or polystyrene sequence was investigated. Atomic force microscopy and theoretical modeling based on molecular mechanics/molecular dynamics calculations were combined. The typical morphology obtained revealed the presence of bright elongated structures.
引用
收藏
页码：1042 / 1046
页数：5
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