Thioacetyl-Terminated Ferrocene-Anthraquinone Conjugates: Synthesis, Photo- and Electrochemical Properties Triggered by Protonation-Induced Intramolecular Electron Transfer

Thioacetyl-Terminated Ferrocene-Anthraquinone Conjugates: Synthesis, Photo- and Electrochemical Properties Triggered by Protonation-Induced Intramolecular Electron Transfer

Two thioacetyl-terminated ferrocene-anthraquinone donor-acceptor molecules with different π-electron conjugative units have been synthesized via a series of Stille and Sonagashira reactions. Their photochemical and electrochemical properties before and after addition of an organic acid are investiga...

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Bibliographic Details
Main Authors: Masaki Murata, Hiroshi Nishihara, Kosuke Namiki, Takako Fujita, Mio Kondo, Wen-Wei Zhang
Format: Article
Language:English
Published: MDPI AG 2010-01-01
Series:Molecules
Subjects:
ferrocene
anthraquinone
donor-acceptor
protonation
valence tautomerization
Online Access:http://www.mdpi.com/1420-3049/15/1/150/

Internet

http://www.mdpi.com/1420-3049/15/1/150/

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