Two-Dimensional Bilayer Smectic Ordering of Rigid Rod-Rod Helical Diblock Polyisocyanides

被引:29
作者
Banno, Motonori [1 ]
Wu, Zong-Quan [1 ]
Nagai, Kanji [1 ]
Sakurai, Shin-ichiro [2 ]
Okoshi, Kento [2 ]
Yashima, Eiji [1 ,2 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Mol Design & Engn, Chikusa Ku, Nagoya, Aichi 4648603, Japan
[2] Japan Sci & Technol Agcy JST, Exploratory Res Adv Technol ERATO, Yashima Super Struct Helix Project, Tokyo, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
COIL BLOCK-COPOLYMERS; AMINE-INITIATED POLYMERIZATION; SENSE-CONTROLLED POLYMERIZATION; MU-ETHYNEDIYL COMPLEXES; N-CARBOXY-ANHYDRIDES; SELECTIVE POLYMERIZATION; SUPRAMOLECULAR MATERIALS; MICROPHASE SEPARATION; LIQUID-CRYSTALLINE; POLYMERS;
D O I
10.1021/ma1009116
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The rigid-rod-like left-handed helical polyisocyanides (poly-3) with a different molecular weight and a narrow molecular weight distribution were prepared by the living polymerization of an enantiomerically pure phenyl isocyanide bearing an L-alanine pendant with an n-hexyl chain (3) using the mu-ethynediyl Pt-Pd catalyst. The left-handed helical poly-3s maintain their living feature and further copolymerized an analogous L-alanine-bound phenyl isocyanide with a long n-tetradecyl chain (4) to produce rod-rod diblock polyisocyanides with a controlled helical sense and a narrow molecular weight distribution. The rigid rod-rod helical diblock copolyisocyanides were composed of the same L-alanine pendants, but with alkyl chains of different lengths self-assembled to form the nanometer-scaled bilayer smectic-like ordering on a substrate and in a liquid crystalline state as evidenced by the direct atomic force microscopic and polarized optical micrograph observations, respectively.
引用
收藏
页码:6553 / 6561
页数:9
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