Conducting supramolecular nanofibers and nanorods

被引:157
作者
Hasegawa, Masashi [2 ]
Iyoda, Masahiko [1 ]
机构
[1] Tokyo Metropolitan Univ, Grad Sch Sci, Dept Chem, Tokyo 1920397, Japan
[2] Kitasato Univ, Sch Sci, Dept Chem, Kanagawa 2288555, Japan
关键词
SELF-ASSEMBLED FIBERS; CHARGE-TRANSPORT; BUILDING-BLOCKS; CONJUGATED POLYMERS; MOLECULAR WIRES; GEL; NANOSTRUCTURES; SEMICONDUCTORS; NANOPARTICLES; ELECTRONICS;
D O I
10.1039/b909347h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recent progress in the study of electroconducting nanomaterials such as nanofibers, nanorods and other nanostructures based on the supramolecular self-assembly of hexabenzocoronenes, oligo(thiophene)s, tetrathiafulvalenes and perylene-3,4,9,10-tetracarboxylic diimides is described in this tutorial review. Conducting nanofibers and nanorods are constructed by doping pi-donors or pi-acceptors with oxidants or reductants before/after the formation of such nanostructures; however, some nanofibers show electric conductivity without any doping in the neutral state. Although cation radicals and anion radicals seem to be difficult to form nanofibers and nanorods, a limited number of cation radicals produce conducting nanofibers. For nanofibers and nanorods composed of weak pi-donors and pi-acceptors, their conductivities are measured by time-resolved microwave conductivity techniques.
引用
收藏
页码:2420 / 2427
页数:8
相关论文
共 59 条
  • [1] Molecularly assembled nanostructures of a redox-active organogelator
    Akutagawa, T
    Kakiuchi, K
    Hasegawa, T
    Noro, S
    Nakamura, T
    Hasegawa, H
    Mashiko, S
    Becher, J
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (44) : 7283 - 7287
  • [2] Formation of oriented molecular nanowires on mica surface
    Akutagawa, T
    Ohta, T
    Hasegawa, T
    Nakamura, T
    Christensen, CA
    Becher, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) : 5028 - 5033
  • [3] Introduction: Molecular conductors
    Batail, P
    [J]. CHEMICAL REVIEWS, 2004, 104 (11) : 4887 - 4890
  • [4] Tetrathiafulvalene (TTF) derivatives: key building-blocks for switchable processes
    Canevet, David
    Salle, Marc
    Zhang, Guanxin
    Zhang, Deqing
    Zhu, Daoben
    [J]. CHEMICAL COMMUNICATIONS, 2009, (17) : 2245 - 2269
  • [5] Enhancing one-dimensional charge transport through intermolecular π-electron delocalization:: Conductivity improvement for organic nanobelts
    Che, Yanke
    Datar, Aniket
    Yang, Xiaomei
    Naddo, Tammene
    Zhao, Jincai
    Zang, Ling
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (20) : 6354 - +
  • [6] SUPRAMOLECULAR SYNTHONS IN CRYSTAL ENGINEERING - A NEW ORGANIC-SYNTHESIS
    DESIRAJU, GR
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (21): : 2311 - 2327
  • [7] Synthesis of tris(tetrathiafulvaleno)dodecadehydro-[18]annulenes and their self-assembly
    Enozawa, H
    Hasegawa, M
    Takamatsu, D
    Fukui, K
    Iyoda, M
    [J]. ORGANIC LETTERS, 2006, 8 (09) : 1917 - 1920
  • [8] ENOZAWA H, UNPUB
  • [9] Magnetic Alignment in Solid State and Temperature Hysteresis in Aqueous Tetrahydrofuran Solution for Tetrathiafulvaleno[18]annulenes
    Enozawa, Hideo
    Hasegawa, Masashi
    Isomura, Eigo
    Nishinaga, Tohru
    Kato, Tadashi
    Yamato, Masafumi
    Kimura, Tsunehisa
    Iyoda, Masahiko
    [J]. CHEMPHYSCHEM, 2009, 10 (15) : 2607 - 2611
  • [10] Semiconducting Neutral Microstructures Fabricated by Coordinative Self-Assembly of Intramolecular Charge-Transfer Tetrathiafulvalene Derivatives
    Geng, Yan
    Wang, Xiao-Jun
    Chen, Bin
    Xue, Hai
    Zhao, Yao-Peng
    Lee, Shuittong
    Tung, Chen-Ho
    Wu, Li-Zhu
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2009, 15 (20) : 5124 - 5129