Self-Assembled Anionic Micellar Template for Polypyrrole, Polyaniline, and Their Random Copolymer Nanomaterials

被引:33
作者
Antony, M. Jinish [2 ]
Jayakannan, M. [1 ]
机构
[1] IISER, Dept Chem, Pune 411008, Maharashtra, India
[2] Natl Inst Interdisciplinary Sci & Technol, Div Chem Sci & Technol, Thiruvananthapuram 695019, Kerala, India
关键词
conducting polymers; micelles; morphology; polyaniline; polypyrrole; self-organization; WAXS; AMPHIPHILIC MOLECULAR DESIGN; SULFONIC-ACID; CHEMICAL-SYNTHESIS; SPECTROSCOPIC INVESTIGATIONS; CONDUCTING POLYMER; PYRROLE; NANOFIBERS; FABRICATION; SURFACTANT; NANOTUBES;
D O I
10.1002/polb.21689
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
We report an anionic surfactant approach for size and shape control in polyaniline, polypyrrole, and their polyaniline-co-polypyrrole random copolymer nanomaterials. A renewable resource azobenzenesulfonic acid anionic surfactant was developed for template-assisted synthesis of these classes of nanomaterials. The surfactant exists as 4.3 nm micelle in water and self-organizes with pyrrole to produce spherical aggregates. The sizes of the spherical aggregates were controlled by water dilution and subsequent oxidation of these templates, produced polypyrrole nanospheres of 0.5 mu M to 50 rum dimensions. The anionic surfactant interacts differently with aniline and forms cylindrical aggregates, which exclusively produce nanofibers of similar to 180 mn in diameter with length up to 3-5 mu M. The template selectivity of surfactant toward aniline and pyrrole was used to tune the nanostructure of the anilinepyrrole random copolymers from nanofiber-to-nanorod-to-nanospheres. Dynamic light scattering technique and electron microscopes were used to study the mechanistic aspects of the template-assisted polymerization. The four probe conductivity of the copolymers showed a nonlinear trend and the conductivity passes through minimum at 60-80% of pyrrole in the feed. The amphiphilic dopant effectively penetrates into the crystal lattices of the polymer chain and induces high solid state ordering in the homopolymer nanomaterials. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47:830-846, 2009
引用
收藏
页码:830 / 846
页数:17
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