z-logo
open-access-imgOpen Access
Characterization and Antimicrobial Activity of Erbium(III)Complexes of C‐3 Substituted 2‐hydroxy‐1,4‐naphthalenedione‐1‐oxime Derivatives
Author(s) -
S. B. Jagtap,
Neha N. Patil,
B.P. Kapadnis,
B. A. Kulkarni
Publication year - 2000
Publication title -
metal-based drugs
Language(s) - English
Resource type - Journals
ISSN - 0793-0291
DOI - 10.1155/mbd.2001.159
Subject(s) - oxime , aspergillus niger , chemistry , antimicrobial , antibacterial activity , candida albicans , nuclear chemistry , pseudomonas aeruginosa , thermogravimetric analysis , carbon 13 nmr , stereochemistry , medicinal chemistry , organic chemistry , microbiology and biotechnology , bacteria , biochemistry , biology , genetics
Erbium(III) complexes of 2-hydroxy-l,4-naphthalenedione-1-oxime and its C-3 substituted derivatives are synthesized and characterized by elemental analysis, thermogravimetric analysis, infrared spectroscopy, magnetic susceptibility measurements 2-hydroxy-1,4-naphthalenedione-1-oxime derivatives are analysed using (1)H and (13)C NMR spectroscopy. The molecular composition of the synthesized complexes is found to be [ML(3)(H(2)O)(2)]. The antimicrobial activity of these complexes is determined by well diffusion method against the target microorganisms- Staphylococcus aureus, Xanthomonas campestris, Pseudomonas aeruginosa, Candida albicans and Aspergillus niger. The antimicrobial activities of 2- hydroxy-1,4-naphthalenedione-1-oximes and their complexes are compared. It is observed that 2-hydroxy-1,4-naphthalenedione-l-oximes exhibit higher antifungal activity as compared to antibacterial activity. These activities are reduced upon complexation of these oximes with Erbium.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom