Electrochemical and in situ Spectroelectrochemical Properties of Phthalocyanines Bearing N-Benzyl-4-Phenyloxyacetamide Moieties
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        İmran Koç
        
Abstract
The general redox behaviour of phthalocyanines bearing N-benzyl-4-phenyloxyacetamide moieties (H2Pc, ZnPc, NiPc, CuPc, and CoPc) has been identified by cyclic voltammetry and differential pulse voltammetry on Pt in dimethylsulfoxide/tetrabutylammonium perchlorate. These measurements showed that the complexes indicate subsequent one-electron reduction and oxidation processes. Although the voltammetric measurements implied the association of the redox processes of some complexes with aggregation phenomenon, the complete evaluation of the aggregation effects by only these measurements was not possible. In situ UV-Vis spectroelectrochemical measurements enabled us to assign the ligand- and metal-based redox processes, and identify if the aggregation affects these processes. These measurements suggested that the redox processes of H2Pc, NiPc, and CuPc are coupled by aggregation phenomenon, while those of ZnPc and especially CoPc are not, probably due to the difference in their axial coordinating properties.
© by Oldenbourg Wissenschaftsverlag, Istanbul, Germany
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Artikel in diesem Heft
- Kinetic Analysis of High-Rate and of Low-Rate Regimes in CO Oxidation on Pt Group Metals: Evidence for Vibrational Excitation of the O-Rich Adlayer and for Thermal Equilibrium of the CO-Rich Phase
- Effect of Particle Size on Non-Isothermal Decomposition of Potassium Titanium Oxalate
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- Initial State and Transition State Contributions to Reactivity Trends of Base-Catalyzed Hydrolysis of Some Nitro Chromen-2-One Derivatives
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