Catalytic generation of chlorine with slight overpotential by micellar ferrocene
نویسندگان
چکیده
Ferrocene solubilized with poly(vinylpyrrolidone) in aqueous KCl solution exhibited a well-defined voltammetric peak at 1.33 V vs. Ag|AgCl at a platinum electrode. The wave was attributed to the oxidation of chloride to chlorine, demonstrated by smell of chlorine, by a view of formation of gas bubbles, by coloration through the reaction with diethyl-p-phenylene diamine, and by the increase in the anodic current with the concentration of chloride. Since no wave was observed in the ferrocene-free solution or KCl-free solution in this potential domain, the reaction mechanism was suggested to be the oxidation of chloride into chlorine catalyzed by micellar ferrocene. The potential at the foot of the wave (1.08 V) was less positive that the standard potential of Cl2/Cl, and hence the reaction may be useful for enhancing the energetic efficiency at chlor-alkali industry. The value of the peak current was one-sixth the theoretical diffusion-controlled current, and was proportional to the square-root of the potential scan rate. key words: chlorine, catalytic current, micellar ferrocene, surfactant, poly(vinylpyrrolidone) * corresponding author, e-mail [email protected], fax +81 776 27 8494
منابع مشابه
The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(II) and copper(II) complexes.
Copper(ii) and palladium(ii) meso-tetraferrocenylporphyrins ( and ) were employed as catalysts for electrochemical proton reduction in DMF using trifluoroacetic acid (TFA) or triethylamine hydrochloride (TEAHCl) as acids. Gas analysis under electrocatalytic conditions at a glassy carbon working electrode confirmed the product as H2. showed catalytic behavior for both TFA and TEAHCl, whereas onl...
متن کاملElectrochemical chlorine evolution at rutile oxide (110) surfaces.
Based on density functional theory (DFT) calculations we study the electrochemical chlorine evolution reaction on rutile (110) oxide surfaces. First we construct the Pourbaix surface diagram for IrO(2) and RuO(2), and from this we find the chlorine evolution reaction intermediates and identify the lowest overpotential at which all elementary reaction steps in the chlorine evolution reaction are...
متن کاملOne-pot Three-Component Synthesis of Dihydroquinoxalin-2-amines Containing a Ferrocene unit with the Potential of Biological and Pharmacological Activities
A three-component reaction between 1,2-phenylenediamine, ferrocenecarbaldehyde, and isocyanides in the presence of a catalytic amount of p-toluenesulfonic acid for the synthesis of 3,4-dihydroquinoxalin-2-amine derivatives containing a ferrocene unit is reported. This approach is an effective procedure because the products have a broad spectrum of biological and pharmacological activities such ...
متن کاملSynthesis, Characterization, and Reactivity of Functionalized Trinuclear Iron–Sulfur Clusters – A New Class of Bioinspired Hydrogenase Models
The air- and moisture-stable iron-sulfur carbonyl clusters Fe3S2(CO)7(dppm) (1) and Fe3S2(CO)7(dppf) (2) carrying the bisphosphine ligands bis(diphenylphosphanyl)methane (dppm) and 1,1'-bis(diphenylphosphanyl)ferrocene (dppf) were prepared and fully characterized. Two alternative synthetic routes based on different thionation reactions of triiron dodecacarbonyl were tested. The molecular struct...
متن کاملRuthenium(II) complexes with ferrocene-modified arene ligands: synthesis and electrochemistry
A series of arene–ruthenium complexes of the general formula [RuCl2{g-C6H5(CH2)2R}L] with R1⁄4OH, CH2OH, OC(O)Fc, CH2OC(O)Fc (Fc1⁄4 ferrocenyl) and L1⁄4PPh3, (diphenylphosphino)ferrocene, or bridging 1,10-bis(diphenylphosphino)ferrocene, have been synthesized. Two synthetic pathways have been used for these ferrocene-modified arene–ruthenium complexes: (a) esterification of ferrocene carboxylic...
متن کامل