Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
593586 | Colloids and Surfaces A: Physicochemical and Engineering Aspects | 2013 | 8 Pages |
Monolayers of a water-soluble metalloporphyrin, manganese tetra-(4-pyridyl) porphine chloride tetrakis (methochloride) (MnTMPyP), and its polymeric derivative with poly (4-vinylpyridine) (MnTMPyP-PVP) have been investigated at the air–water interface. These monolayers were transferred on the substrate surfaces to form hybrid ultrathin films by the Langmuir-Blodgett (LB) method. It was revealed that, although the water-soluble MnTMPyP could not form insoluble monomolecular layer on the pure water surface, it could be stabilized on the NaB(C6H5)4 subphase surface due to an electrostatic interaction between MnTMPyP and B(C6H5)4−, resulting in the formation of MnTMPyP-B(C6H5)4 hybrids. On the other hand, its polymeric derivative of MnTMPyP-PVP could form stable insoluble monolayers on the pure water, NaB(C6H5)4 and Na2PdCl4 subphase surfaces. Composition, structure and microscopic morphology of the as-prepared LB films were characterized by using UV–vis absorption, infrared and X-ray photoelectron spectroscope, as well as scanning electron microscope. The results suggested formation of the hybrid MnTMPyP-B(C6H5)4 and MnTMPyP-(PVP-)B(C6H5)4 and Pd-MnTMPyP-PVP coordination polymer ultrathin films at the interfaces. Cyclic voltammograms of the LB films revealed two couples of reversible redox waves centered at 0.2–0.3 and −0.1 to −0.2 V (vs Ag/AgCl), corresponding to the Mn(II)/Mn(III)TMPyP-(PVP-)B(C6H5)4 and Mn(III)/Mn(IV)TMPyP-(PVP-)B(C6H5)4 electron transfer processes of the manganese porphyrins in the LB films.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Polymeric manganese porphyrin PVP-MnTMPyP was synthesized. ► PVP-MnTMPyP-B(C6H5)4 hybrids were assembled. ► Pd-MnTMPyP-PVP coordination polymer multilayers were prepared. ► The hybrid and coordination polymer multilayer modified electrode showed reversible redox reaction.