Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Self-organizing super-structures formed from hydrogen-bonded biimidazolate metal complexes.

Makoto Tadokoro1, Hideaki Kanno, Tadanori Kitajima

  • 1Department of Chemistry, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan. tadokoro@sci.osaka-cu.ac.jp

Proceedings of the National Academy of Sciences of the United States of America
|April 4, 2002
PubMed
Summary

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Proton Conductive Supramolecular Architectures Based on a Cobalt Terpyridine-Biimidazole Complex: Hydrogen-Bonded Hexamer and Mixed-Valence 1D Chain.

Chemistry (Weinheim an der Bergstrasse, Germany)·2025
Same author

Solid-State <sup>2</sup>H NMR Analysis for Hierarchical Water Clusters Confined to Quasi-One-Dimensional Molecular Nanoporous Crystals.

Journal of the American Chemical Society·2025
Same author

Two-step insertion/release of electrolytic cations in redox-active hydrogen-bonding nanoporous coordination crystals.

Physical chemistry chemical physics : PCCP·2025
Same author

Dual Emission with Efficient Phosphorescence Promoted by Intermolecular Halogen Interactions in Luminescent Tetranuclear Zinc(II) Clusters.

Inorganic chemistry·2024
Same author

Covalently Linked 5,6,11,12-Tetraazanaphthacene Dimer and Its Triptycene-Capped Derivatives as Electron Acceptors.

Chemistry (Weinheim an der Bergstrasse, Germany)·2024
Same author

Solvent vapour-responsive structural transformations in molecular crystals composed of a luminescent mononuclear aluminium(III) complex.

Dalton transactions (Cambridge, England : 2003)·2024

Researchers created five new molecular crystal superstructures using metal complexes and self-organization. These controlled structures, including chains, ribbons, helices, and sheets, advance molecular functional materials development.

Area of Science:

  • Materials Science
  • Crystallography
  • Supramolecular Chemistry

Background:

  • Self-organization is key for developing novel molecular functional materials.
  • Hydrogen bonding and metal coordination are effective for designing preprogrammed superstructures.
  • Controlling crystal architecture is crucial for material properties.

Purpose of the Study:

  • To create diverse, controlled molecular crystal superstructures.
  • To explore the use of metal complexes with 2,2'-biimidazolate mono-anions for superstructure formation.
  • To demonstrate the versatility of combined hydrogen bonding and metal coordination.

Main Methods:

  • Utilized neutral metal complexes featuring 2,2'-biimidazolate mono-anions.
  • Employed self-organization principles guided by hydrogen bonding and metal coordination.

Related Experiment Videos

  • Characterized the resulting crystalline structures.
  • Main Results:

    • Successfully synthesized five distinct superstructures: one-dimensional linear chains, zigzag ribbons, right-handed and left-handed helices, and a two-dimensional honeycomb sheet.
    • Demonstrated precise control over superstructure formation through molecular design.
    • Established a method for generating complex architectures from simple building blocks.

    Conclusions:

    • The study successfully generated five novel molecular crystal superstructures.
    • This work highlights the power of combining hydrogen bonding and metal coordination for predictable crystal engineering.
    • The developed method offers a pathway for designing advanced molecular functional materials with tailored architectures.