Poly(aryleneethynylene) Type Polymers Containing a Ferrocene Unit in the π-Conjugated Main Chain. Preparation, Optical Properties, Redox Behavior, and Mössbauer Spectroscopic Analysis

This publication has 58 references indexed in Scilit:

• Unique Temperature Dependence of NMR and UV-visible Spectra of Poly(3-hexylthiophene-2,5-diyl) and Its Related Compounds
  Chemistry Letters, 1996
• Conjugated Polymers with Main Chain Chirality. 3. Synthesis of Optically Active Poly(aryleneethynylene)s
  Macromolecules, 1996
• Routes to Conjugated Polymers with Ferrocenes in Their Backbones: Synthesis and Characterization of Poly(ferrocenylenedivinylene) and Poly(ferrocenylenebutenylene)
  Macromolecules, 1995
• The Synthesis and Properties of Face-to-Face Metallocene Polymers
  Macromolecules, 1995
• Preparation and optical properties of soluble π-conjugated poly(aryleneethynylene) type polymers
  Journal of the Chemical Society, Chemical Communications, 1993
• Poly(2,5-ethynylenethiophenediylethynylenes), related heteroaromatic analogs, and poly(thieno[3,2-b]thiophenes): synthesis and thermal and electrical properties
  Macromolecules, 1992
• Palladium Catalyzed C–C Coupling for Synthesis of π-Conjugated Polymers Composed of Arylene and Ethynylene Units
  Bulletin of the Chemical Society of Japan, 1984
• Electron transfer in oxidized biferrocene, biferrocenylene, and [1.1]ferrocenophane systems
  Inorganic Chemistry, 1975
• Organic solid state. VII. Semiconducting polymers. Mixed valence ferrocene-ferricenium polymers
  Journal of the American Chemical Society, 1972
• Fe57 Mössbauer Effect in Ferrocene Derivatives
  The Journal of Chemical Physics, 1963