Title of article :
Synthesis, characterization and electrochemical behavior of new transition metal complexes derivatives of 4-hydroxy-6-methyl-3-[(2E)-3-(4- (dimethylamino) phenyl) prop-2-enoyl]-2H-pyran-2-one
Author/Authors :
tabti, s. mohamed el bachir el ibrahimi university - laboratory of electronic materials and systems, Bordj Bou Arreridj, Algeria , benmahmoud, m. mohamed el bachir el ibrahimi university - faculty of science technology - department sm, Bordj Bou Arreridj, Algeria , djedouani, a. university city ali mendjeli - superior school of constantine, Constantine, Algeria , djedouani, a. constantine university 1 - laboratory of analytical physicochemistry and crystallochemistry of organometallic and biomolecular materials, Constantine, Algeria , semmari, l. mohamed el bachir el ibrahimi university - faculty of science technology - department sm, Bordj Bou Arreridj, Algeria , hamimid, a. mohamed el bachir el ibrahimi university - faculty of science technology - department sm, Bordj Bou Arreridj, Algeria
From page :
2624
To page :
2630
Abstract :
The reaction of Ni (II) acetate, Co (II) chloride and copper (II) nitrate with 4-hydroxy- 6-methyl-3-[(2E)-3-(4-(dimethylamino) phenyl)prop-2-enoyl]-2H-pyran-2-one leads to the synthesis of new complexes Ni(HL)₂, Cu(HL)₂(H₂O) and Co(HL)₂(NH₃)₄. The molecular structures of the synthesized compounds were elucidated by various physicochemical properties such as the UV-Vis, FT-IR, , and elemental analysis. Electrochemical behavior of the complexes of (Cu, Ni) has been investigated by cyclic voltammetry on glassy carbon electrode in DMF at 100 mV/s scan rate. This study indicate that the reduction process corresponding to Cu^II/Cu^I is electrochemically quasi-reversible in complex of copper, and irreversible reduction process for Ni^II/Ni^I.
Keywords :
Metal complex , IR , UV , Vis , ESR , Elemental analysis , Electrochemistry
Journal title :
Journal of Materials and Environmental Science
Journal title :
Journal of Materials and Environmental Science
Record number :
2583477
Link To Document :
بازگشت