On the influence of porphyrin π-π stacking on supramolecular chirality created in the porphyrin-based twisted tape structure

被引：62
作者：
Takeuchi, M [1 ]
Tanaka, S [1 ]
Shinkai, S [1 ]
机构：
[1] Kyushu Univ, Grad Sch Engn, Dept Chem & Biochem, Higashi Ku, Fukuoka 8128581, Japan
来源：
CHEMICAL COMMUNICATIONS | 2005年 / 44期
关键词：
D O I：
10.1039/b512128k
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Achiral porphyrin derivatives 1-M form twisted supramolecular assemblies and the pitch of the twisted tape structure can be altered by changing the central metal.
引用
收藏
页码：5539 / 5541
页数：3
相关论文
共 39 条
[1]   Hydrogen-bonded porphyrinic solids: Supramolecular networks of octahydroxy porphyrins [J].
Bhyrappa, P ;
Wilson, SR ;
Suslick, KS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (36) :8492-8502
[2]   Supramolecular networks of octahydroxy porphyrins [J].
Bhyrappa, P ;
Wilson, SR ;
Suslick, KS .
SUPRAMOLECULAR CHEMISTRY, 1998, 9 (03) :169-174
[3]   Supramolecular polymers [J].
Brunsveld, L ;
Folmer, BJB ;
Meijer, EW ;
Sijbesma, RP .
CHEMICAL REVIEWS, 2001, 101 (12) :4071-4097
[4]   Chiral architectures from macromolecular building blocks [J].
Cornelissen, JJLM ;
Rowan, AE ;
Nolte, RJM ;
Sommerdijk, NAJM .
CHEMICAL REVIEWS, 2001, 101 (12) :4039-4070
[5]   Self-assembled diamide nanotubes in organic solvents [J].
Díaz, N ;
Simon, FX ;
Schmutz, M ;
Rawiso, M ;
Decher, G ;
Jestin, J ;
Mésini, PJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (21) :3260-3264
[6]  
ESCH J, 1999, SUPRAMOLECULAR SCI I, P233
[7]   Self-assembled nanotapes of oligo(p-phenylene vinylene)s:: Sol-gel controlled optical properties in fluorescent π-electronic gels [J].
George, SJ ;
Ajayaghosh, A .
CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (11) :3217-3227
[8]  
Gronwald O, 2001, CHEM-EUR J, V7, P4328, DOI 10.1002/1521-3765(20011015)7:20<4328::AID-CHEM4328>3.0.CO
[9]  
2-S
[10]   Further evidence for the gelation ability-structure correlation in sugar-based gelators [J].
Gronwald, O ;
Sakurai, K ;
Luboradzki, R ;
Kimura, T ;
Shinkai, S .
CARBOHYDRATE RESEARCH, 2001, 331 (03) :307-318
1234