Dechlorination of β-methylallyl chloride by electrogenerated [Co(I)(bipyridine) 3] +: An electrochemical study in the presence of cationic surfactants

• Published in: Journal of colloid and interface science Vol. 297; no. 2; pp. 687 - 695
• Main Authors: Muthuraman, G., Chandrasekara Pillai, K.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 15.05.2006; Elsevier
• Subjects: Catalysis; Chemistry; EC CAT mechanism; Electrochemical mediated catalysis; Exact sciences and technology; GC/MS; General and physical chemistry; Micellar stabilization; Outer sphere electron transfer mechanism; Second-order rate constant; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Micellar stabilization; GC/MS; Electrochemical mediated catalysis; EC CAT mechanism; Second-order rate constant; Outer sphere electron transfer mechanism; Catalytic reaction; ECCAT mechanism; Stabilization; Cationic surfactant; Electron transfer; Ionic surfactant; Mechanism; Dechlorination; Chlorides; Electrochemistry; Catalysis; Rate constant
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2005.11.010

We have investigated the electrocatalytic dehalogenation of β-methylallyl chloride ( β-mAC), widely used in the polymer industry, using [Co(I)(bpy) 3] + (where bpy = 2,2′-bipyridine) electrochemically generated in situ from [Co(II)(bpy) 3] 2+ at a glassy carbon electrode in the presence of three different cationic surfactants in aqueous solution. Cetyltrimethylammonium bromide (CTAB), tetradecyltrimethylammonium bromide (TDTAB), and cetylbenzyldimethylammonium chloride (CBDAC) were employed in the present investigation. The [Co(II)(bpy) 3] 2+–cationic surfactant systems show excellent electrocatalytic activity toward dehalogenation of β-mAC. The dependence of the catalytic current, the corresponding potential, and the current function on the potential scan rate has been analyzed to assess the nature of the catalytic reaction. The second-order rate constant, k chem, for the reaction between the β-mAC substrate and the electrogenerated-micelle stabilized-Co(I) complex has been calculated by a cyclic voltammetry technique. The reduction products after 3 h of bulk electrolysis have been identified by GC/MS to be one nonchloro compound (2-methyl-1,5-hexadiene ( IV)) and two chloro compounds (1-chloro-2,5-dimethyl-2,5-hexadiene ( V) and spiro[1.2]cylopropyl-6-chloro-5-methyl-hex-4-ene ( VI)). Based on the electrochemical results and the mass spectral data, a reaction scheme involving all the reduction products has been proposed. Finally, a good correlation between the catalytic efficiency and the structural features of the surfactant molecules is demonstrated. The present study emphasizes the need for further optimization work to achieve maximum yield of nonchloro compound ( IV) to employ the present [Co(II)(bpy) 3] 2+–cationic surfactant systems with a high catalytic efficiency as promising for possible applications. Electrochemically generated Co(I) bipyridine complex stabilized by micellar aggregates of cationic surfactant (CTAB or TDTAB or CBDAC) has been used for mediated reduction of β-methylallyl chloride in aqueous solutions, and a good correlation between structural features of surfactant molecules and the efficiency of the catalytic mediation reaction has been demonstrated.