Jove
Visualize
Contact Us

Related Experiment Videos

Electropolymerized Films of Macromeric Assemblies.

Toru Kajita1, Robert M. Leasure, Martin Devenney

  • 1Kenan Laboratories of Chemistry, The University of North Carolina at Chapel Hill, Venable Hall, CB# 3290, Chapel Hill, North Carolina 27599-3290.

Inorganic Chemistry
|October 24, 2001
PubMed
Summary
This summary is machine-generated.

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

Calcium Carbonate Cement: A Carbon Capture, Utilization, and Storage (CCUS) Technique.

Materials (Basel, Switzerland)·2021
Same author

Novel bipolar bathophenanthroline containing hosts for highly efficient phosphorescent OLEDs.

Organic letters·2008
Same author

Isolation and Characterization of the Osmium(V)-Imido Complex [Os(V)(Tp)(Cl)(2)(NH)] We are grateful to the National Science Foundation under Grant number CHE-9503738, the Los Alamos National Laboratory (DOE) under Grant Number 10730-001-00-2C, and the Laboratory Directed Research and Development Program for support of this research. M. H. V. Huynh gratefully acknowledges postdoctoral fellowship support from the Directorapos;s Office of Los Alamos National Laboratory. Los Alamos National Laboratory is operated by the University of California for the U.S. Department of Energy under Contract W-7405-ENG-36. We also thank Dr. Paul R. Sharp (Professor of Chemistry, University of Missouri, Columbia, MO, 65211) for the information on transition metal parent imido complexes.

Angewandte Chemie (International ed. in English)·2002
Same author

Medium Effects on Charge Transfer in Metal Complexes.

Chemical reviews·2002
Same author

Localization in trans,trans-[(tpy)(Cl)(2)Os(III)(N(2))Os(II)(Cl)(2)(tpy)](+) (tpy = 2,2':6',2"-Terpyridine).

Inorganic chemistry·2001
Same author

Ruthenium(II) MLCT Excited States. Stabilization toward Ligand Loss in Rigid Media.

Inorganic chemistry·2001
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

New macromeric films of poly[Ru(II)(vbpy)(2)(4-CO(2)H-4'-CH(3)bpy)](2+) exhibit unique microporous structures and altered excited state lifetimes compared to conventional polymer films.

Area of Science:

  • Electrochemistry
  • Polymer Science
  • Materials Science
  • Photochemistry

Background:

  • Ruthenium(II) bipyridine complexes are widely studied for their photophysical and electrochemical properties.
  • Polymer-supported metal complexes offer advantages in device fabrication and stability.
  • Living anionic polymerization provides precise control over polymer architecture.

Purpose of the Study:

  • To synthesize and characterize a novel macromer based on poly[4-(2-aminoethyl)styrene] and a ruthenium(II) bipyridine complex.
  • To investigate the electropolymerization behavior and film properties of the synthesized macromer.
  • To compare the electrochemical and photophysical properties of macromeric films with conventional polymer films.

Main Methods:

Related Experiment Videos

  • Synthesis of poly[4-(2-aminoethyl)styrene] via living anionic polymerization.
  • Derivatization of the polymer with [Ru(II)(vbpy)(2)(4-CO(2)H-4 ombin-CH(3)bpy)](2+) via amide coupling.
  • Reductive electropolymerization of the macromer onto various electrode materials.
  • Characterization of film morphology, charge transfer, and excited state lifetimes.
  • Main Results:

    • Macromeric films displayed significantly rougher, locally microporous structures compared to conventional films.
    • Intrafilm charge transfer rates in macromeric films were comparable to conventional films.
    • Metal-to-ligand charge transfer (MLCT) excited state lifetimes were shortened in macromeric films, attributed to quenching by trap sites.

    Conclusions:

    • The synthesized macromer can be effectively electropolymerized to form stable films with unique structural properties.
    • The macromeric films exhibit distinct photophysical characteristics, including shorter excited state lifetimes, due to their structure.
    • Sequential polymerization allows for the preparation of stable mixed-polymer films with tunable properties.