Synthesis, Characterization and Electrical Conductance of Ferrocenylazobenzene

Ferrocenylazobenzene was synthesized by condensing an aminoazobenzene dye with ferrocenecarboxylic acid previously treated with oxalyl chloride. The compound displayed an anticipated chemically reversible one-electron oxidation process and gave a formal potential, E° = 0.65 V. In the UV-Vis region,...

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Bibliographic Details
Main Authors: Hegde, Gurumurthy, Tagg, Tei, Siti Athirah, Mohamad Jamali, Hasiah, Salleh
Format: Article
Published: Taylor & Francis 2014
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Online Access:http://umpir.ump.edu.my/id/eprint/8078/
http://dx.doi.org/10.1080/15421406.2014.968081
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Summary:Ferrocenylazobenzene was synthesized by condensing an aminoazobenzene dye with ferrocenecarboxylic acid previously treated with oxalyl chloride. The compound displayed an anticipated chemically reversible one-electron oxidation process and gave a formal potential, E° = 0.65 V. In the UV-Vis region, the azo π-π* and n-π* transitions appeared at 355 and 460 nm respectively. On oxidation of the ferrocenyl moiety, the azo π-π* band was blue-shifted to 348 nm with an increase in intensity, while a new broad, lower energy absorption band assigned to the ligand-to-metal charge transfer appeared at 622 nm. The growth of this new band was concurrent with the bleaching of the metal-to-ligand charge transfer band which was largely obscured by the azo n-π* band at 460 nm. The compound in the form of thin film gave an average electrical conductivity of 0.239 ± 0.001 Scm−1 and a non-linear I-V curve with knee voltage at 2.3 V in dark condition.