Electrochemical study and dependence of ‘transition state’ in Co(II) and Ni(II) complexes with some antibiotics and cephalothin

Electrode kinetics and study of ‘transition state’ with applied potential in case of [M – antibiotics – cephalothin] system were reported at pH = 7.30 ± 0.01 at suitable supporting electrolyte at 25.0 0 C. The M = Co or Ni and antibiotics were doxycycline, chlortetracycline, oxytetracycline, tetracy...

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Bibliographic Details
Main Author: F. Khan
Format: Article
Language:English
Published: Universidade Estadual Paulista 2018-09-01
Series:Eclética Química
Online Access:https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/993
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Summary:Electrode kinetics and study of ‘transition state’ with applied potential in case of [M – antibiotics – cephalothin] system were reported at pH = 7.30 ± 0.01 at suitable supporting electrolyte at 25.0 0 C. The M = Co or Ni and antibiotics were doxycycline, chlortetracycline, oxytetracycline, tetracycline, minocycline, amoxicillin and chloramphenicol used as primary ligands and cephalothin as secondary ligand. Kinetic parameters viz. transfer coefficient (a), degree of irreversibility (l), diffusion coefficient (D) and rate constant (k) were determined. The values of a and k varied from 0.41 to 0.59 and 2.60 X 10 -3 cm s -1 to 9.67 X 10 -3 cm s -1 in case of [Co – antibiotics – cephalothin] system. In case of [Ni – antibiotics – cephalothin], a and k varied from 0.41 to 0.58 and 2.34 X 10 -3 cm s -1 to 9.19 X 10 -3 cm s -1 respectively confirmed that transition state behaves between oxidant and reductant response to applied potential and it adjusts it self in such a way that the same is located midway between dropping mercury electrode and solution interface. The values of rate constant confirmed the quasireversible nature of electrode processes. The stability constants (logb) of complexes were also determined.
ISSN:1678-4618