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Helical Polymers: Synthesis, Structures, and Functions
被引:1427
作者:
Yashima, Eiji
[1
]
Maeda, Katsuhiro
[2
]
Iida, Hiroki
[1
]
Furusho, Yoshio
[1
]
Nagai, Kanji
[1
]
机构:
[1] Nagoya Univ, Dept Mol Design & Engn, Grad Sch Engn, Chikusa Ku, Nagoya, Aichi 4648603, Japan
[2] Kanazawa Univ, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201192, Japan
基金:
日本学术振兴会;
关键词:
SENSE-SELECTIVE POLYMERIZATION;
POLY(PHENYLACETYLENE) DERIVATIVES BEARING;
LIQUID-CRYSTALLINE PROPERTIES;
CHIRAL STATIONARY PHASES;
RIGID BACKBONE POLYMERS;
OLIGOPYRIDINE-DICARBOXAMIDE STRANDS;
AZA-18-CROWN-6 ETHER PENDANTS;
MOLECULAR-WEIGHT DEPENDENCE;
OPTICALLY-ACTIVE POLYMERS;
ATOMIC-FORCE MICROSCOPY;
D O I:
10.1021/cr900162q
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The synthesis process, structures and functions of helical polymers was reviewed. The static and dynamic helical polymers differ through their helix inversion barriers. As a consequence, the former helical conformations are locked during the polymerization under kinetic control, while the latter helical conformations are thermodynamically controlled. It has also been studied that helical conformations of dynamic helical polymers can also be locked, as demonstrated by the unique memory effect observed in dynamic helical poly(phenylacetylene)s and poly(phenyl isocyanide)s induced by chiral guest molecules. In addition, either static or dynamic helical polymers with an excess single-handedness can be prepared by the polymerization of monomers with the identical framework, but bearing different substituents. Apart from the breadth of single-stranded helical polymers and oligomers, the design and synthetic strategies for doublestranded helical polymers and oligomers remain limited, regardless of the natural model, the double-helical DNA.
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页码:6102 / 6211
页数:110
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