Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21399
Title: Synthesis, characterization and electrochemical behaviour of some substituted 2-phenyl-4-(4'-arylazophenyl)-3-thioxo-2H-3,4-dihydro-2,4,9,10-tetraazaphenanthren- 1-ones
Authors: Sharma, Pratibha
Kumar, Ashok
Sharma, Manisha
Upadhyay, Siya
Issue Date: Dec-2004
Publisher: NISCAIR-CSIR, India
IPC Code: Int.Cl.7 C07 D 221/10
Abstract: A new facile method for the synthesis of 2-phenyl-4-(4'-arylazpheny l)-3-thioxo-2H-3,4-dihydro-2,4,9, 10-tetraazaphenanthren-1-ones has been developed. Structures of all the sy nthesized compounds have been established on the basis of their consistent elemental, IR and NMR spectral data. The electrochemical reductions of synthesized compounds have been studied over a wide pH range in B.R. buffers at dropping-mercury and glassy carbon electrodes. All the compounds are found to undergo cathodic reduction by the uptake of two-electrons in diffusion-controlled and irreversible manner. On the basis of polarography, cyclic voltammetry and coulometry, a plausible reduction mechanism is suggested to account for the reduction of azo site in the compounds. Kinetic parameters i.e., charge-transfer coefficient (αn), forward rate constant (Kof,h), diffusion-coefficient (D01/2) and diffusion current constant (I) have also been calculated . An interesting correlation between half-wave potential (E1/2) values of various substituents and Hammett substituents constant (σ) have also been interpreted.
Page(s): 2653-2660
URI: http://hdl.handle.net/123456789/21399
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.43B(12) December 2004]

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