Issue 7, 2011

Enable PVC plastic for a novel role: its functionalisation with diiron models of the sub-unit of [FeFe]–hydrogenase, assembly of film electrodes, and electrochemical investigations

Abstract

Three polymers functionalised with diiron carbonyl units, PVC–Fe-A, -B, and -C, were prepared using commercially available polymer PVC (polyvinyl chloride). PVC–Fe-A resulted from the reaction of the reduced form of a diiron complex, [Fe2(μ-S)2(CO)6], with PVC, whereas PVC–Fe-B and PVC–Fe-C were, respectively, prepared by reacting PVC–N3, the polymer functionalised with azide groups by substitution of the chloride of the polymer, with two diiron complexes, [Fe2(μ-SCH2C[double bond, length as m-dash]CH)2(CO)6] (1) and [Fe2(μ-SnBut)(μ-SCH2C[double bond, length as m-dash]CH)(CO)6] (2, nBut = –CH2CH2CH2CH3), via “click chemistry” under the catalysis of CuI. Those polymers were characterised using infrared spectroscopy (IR), scanning electron microscopy (SEM), and thermal gravimetric analysis (TGA). Film electrodes were assembled using a spin-coating technique by casting a mixture of the functionalised polymer, MWCNTs (multi-wall carbon nanotubes), and Nafion onto the surface of a vitreous carbon electrode. The assembled electrodes exhibited electrochemical responses and catalysis on proton reduction in a medium of acetonitrile-acetic acid with a positive shift in reduction potential by over 400 mV compared to the precursor diiron complexes (1 and 2).

Graphical abstract: Enable PVC plastic for a novel role: its functionalisation with diiron models of the sub-unit of [FeFe]–hydrogenase, assembly of film electrodes, and electrochemical investigations

Supplementary files

Article information

Article type
Paper
Submitted
23 Jun 2011
Accepted
04 Aug 2011
First published
16 Sep 2011

RSC Adv., 2011,1, 1211-1219

Enable PVC plastic for a novel role: its functionalisation with diiron models of the sub-unit of [FeFe]–hydrogenase, assembly of film electrodes, and electrochemical investigations

L. Wang, Z. Xiao, X. Ru and X. Liu, RSC Adv., 2011, 1, 1211 DOI: 10.1039/C1RA00343G

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