Nanoscopic fibrous assemblies made of metallophthalocyanine-terminated amphiphilic polymers

被引:23
|
作者
Kimura, M [1 ]
Ueki, H
Ohta, K
Hanabusa, K
Shirai, H
Kobayashi, N
机构
[1] Shinshu Univ, Fac Text Sci & Technol, Dept Funct Polymer Sci, Ueda, Nagano 3868567, Japan
[2] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai, Miyagi 9808587, Japan
关键词
living polymerization; nanostructures; phthalocyanines; self-assembly; supramolecular chemistry;
D O I
10.1002/chem.200400341
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Atom-transfer radical polymerization (ATRP) of acrylates from the initiator-modified zinc phthalocyanine yielded amphiphilic, phthalocyanine-terminated polymers with a narrow molecular-weight distribution. The disklike phthalocyanine moiety was incorporated into one end of the polymer chain. We investigated the aggregation behavior of phthalocyanine-terminated polymers in solution and in the solid state by using UV-visible, FTIR, differential scanning calorimetry (DSC), and temperature-controlled powder X-ray diffraction (XRD) measurements. Amphiphilic phthalocaynine-terminated polymers that possess a poly[tri(ethylene glycol)methyl ether acrylate] chain aggregate in methanol to form a physical gel. Images from atomic force microscopy (AFM) and transmission electron microscopy (TEM) indicate that the physical gel contains a dense fibrous network structure, in which the zinc phthalocyanine groups were stacked into one-dimensional columnar aggregates through intermolecular a-a interactions between the pi-conjugated phthalocyanines and through van der Waals interaction of alkyl chains.
引用
收藏
页码:4954 / 4959
页数:6
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