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

Philippe Ledere; Anna Calderone; Dirk Marsitzky; Viola Francke; Yves Geerts; Klaus Müllen; Jean-Luc Bredas; Roberto Lazzaroni

doi:10.1002/1521-4095(200007)12:14<1042::AID-ADMA1042>3.0.CO;2-J

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

Philippe Ledere, Anna Calderone, Dirk Marsitzky, Viola Francke, Yves Geerts, Klaus Müllen, Jean-Luc Bredas, Roberto Lazzaroni

Physical Sciences and Engineering

Research output: Contribution to journal › Article › peer-review

125 Scopus citations

Abstract

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.

Original language	English (US)
Pages (from-to)	1042-1046
Number of pages	5
Journal	Advanced Materials
Volume	12
Issue number	14
DOIs	https://doi.org/10.1002/1521-4095(200007)12:14<1042::AID-ADMA1042>3.0.CO;2-J
State	Published - Jul 19 2000

ASJC Scopus subject areas

Materials Science(all)
Mechanics of Materials
Mechanical Engineering

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10.1002/1521-4095(200007)12:14<1042::AID-ADMA1042>3.0.CO;2-J

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AU - Ledere, Philippe

AU - Calderone, Anna

AU - Marsitzky, Dirk

AU - Francke, Viola

AU - Geerts, Yves

AU - Müllen, Klaus

AU - Bredas, Jean-Luc

AU - Lazzaroni, Roberto

PY - 2000/7/19

Y1 - 2000/7/19

N2 - 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.

AB - 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.

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DO - 10.1002/1521-4095(200007)12:14<1042::AID-ADMA1042>3.0.CO;2-J

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JF - Advanced materials (Deerfield Beach, Fla.)

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ER -

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

Abstract

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