Publications by authors named "Vijendran Vijaikanth"

Purpose: Food forensics is an emerging field and the initial part of this review showcases the toxic effects and the instrumental methods applied for the detection of the most commonly used azo dyes. Electrochemical detection has a lot of advantages and hence the significance of the most important techniques used in the electrochemical detection is discussed. The major part of this review highlights the surface modified electrodes, utilized for the detection of the most important azo dyes to achieve low detection limit (LOD).

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Due to environmental contamination and the depletion of energy supplies, it is very important to develop low-cost, high-performance, multifunctional electrocatalysts for energy conversion and storage systems. Herein, we report the development of cost-effective modified electrodes containing g-CN/chlorocobaloxime composites (C1-C4) and their electrocatalytic behavior toward the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), followed by their energy-storage applications. A series of chlorocobaloximes {ClCo(dpgH)B} with diphenylglyoxime (dpgH) and neutral bases (B) containing a carboxylic acid moiety (isonicotinic acid, pyridine-3,5-dicarboxylic acid, indole-2-carboxylic acid, and p-aminobenzoic acid) have been synthesized and characterized by spectroscopic techniques.

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We report stable and heterogeneous graphene oxide (GO)-intercalated copper as an efficient catalyst for the organic transformations in green solvents. The GO-intercalated copper(II) complex of bis(1,4,7,10-tetraazacyclododecane) [Cu(II)-bis-cyclen] was prepared by a facile synthetic approach with a high dilution technique. The as-prepared GO-Cu(II)-bis-cyclen nanocomposite was used as a click catalyst for the 1,3 dipolar Huisgen cycloaddition reaction of terminal alkyne and azide substrates.

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Rate constants kel obtained by impedance spectroscopy for the reduction of Ru(NH3)6(3+) at polycrystalline Pt and Au ultramicroelectrodes depend strongly on the identity and concentration of the anion present in the order CF3SO3(-) < Cl(-) < ClO4(-), but not on the cation of the supporting electrolyte (Na(+), K(+), H(+)). For Cl(-) as the sole anion present, kel is directly proportional to the total [Cl(-)], such that kel would be zero if Cl(-) were hypothetically absent, indicating that Cl(-) is directly involved in mediation of the Ru(NH3)6(3+/2+) electron transfer. For CF3SO3(-) as the sole counterion, the dependence of kel on the total [CF3SO3(-)] is not linear, possibly because blocking of the available electrode surface becomes dominant at high triflate concentrations.

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