Thermodynamically controlled self-assembly of covalent nanoarchitectures in aqueous solution

Ryota Tanoue, Rintaro Higuchi, Nobuo Enoki, Yuya Miyasato, Shinobu Uemura, Nobuo Kimizuka, Adam Z. Stieg, James K. Gimzewski, Masashi Kunitake

    Research output: Contribution to journalArticlepeer-review

    146 Citations (Scopus)

    Abstract

    The pursuit of methods for design and preparation of robust nanoarchitectonic systems with integrated functionality through bottom-up methodologies remains a driving force in molecular nanotechnology. Through the use of,π-conjugated covalent bonds, we demonstrate a general substrate-mediated, soft solution methodology for the preparation of extended π-conjugated polymeric nanoarchitectures in low-dimensions. Based on thermodynamic control over equilibrium polymerization at the solid-liquid interface whereby aromatic building blocks spontaneously and selectively link, close-packed arrays composed of one-dimensional (1-D) aromatic polymers and two-dimensional (2-D) macromolecular frameworks have been prepared and characterized by in situ scanning tunneling microscopy. This methodology eliminates the necessity for severe conditions and sophisticated equipment common to most current fabrication techniques and imparts almost infinite possibilities for the preparation of robust materials with designer molecular architectures.

    Original languageEnglish
    Pages (from-to)3923-3929
    Number of pages7
    JournalACS nano
    Volume5
    Issue number5
    DOIs
    Publication statusPublished - May 24 2011

    All Science Journal Classification (ASJC) codes

    • Materials Science(all)
    • Engineering(all)
    • Physics and Astronomy(all)

    Fingerprint

    Dive into the research topics of 'Thermodynamically controlled self-assembly of covalent nanoarchitectures in aqueous solution'. Together they form a unique fingerprint.

    Cite this