z-logo
Premium
(NH 4 ) 2 [Ni(H 2 O) 6 ] 2 V 10 O 28  ⋅ 4H 2 O; Structural Analysis and Bactericidal Activity against Pathogenic Gram Negative Bacteria
Author(s) -
Mahmoud Ghada AbdElmonsef,
Ibrahim Ahmed B. M.,
Mayer Peter
Publication year - 2021
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202100006
Subject(s) - escherichia coli , triclinic crystal system , nuclear chemistry , serratia marcescens , chloramphenicol , chemistry , crystal structure , stereochemistry , crystallography , antibiotics , biochemistry , gene
A bis(hexaaquanickel(II)) complex‐decavanadate cluster compound, (NH 4 ) 2 [Ni(H 2 O) 6 ] 2 V 10 O 28  ⋅ 4H 2 O, was synthesized. This compound has been structurally characterized by infrared spectroscopy and single crystal XRD analysis that indicated its triclinic P −1 space group. Additionally, the thermal decomposition mechanism of the compound to a composite of V 2 O 5 and Ni(VO 3 ) 2 was elucidated. The common antibacterial agents are organics that experience instability and cause pollution to the environment, therefore we wish to consider the synthesis of inorganic bactericides. (NH 4 ) 2 [Ni(H 2 O) 6 ] 2 V 10 O 28  ⋅ 4H 2 O, in comparison to chloramphenicol, led to better inhibition of the growth of five Gram negative human pathogenic bacterial strains ( Escherichia coli, Klebsiella pneumonia, Serratia marcescens, Serratia plymuthica and Pseudomonas aeruginosa) . Remarkably, the highest inhibition was displayed against Escherichia coli that was inhibited completely at (NH 4 ) 2 [Ni(H 2 O) 6 ] 2 V 10 O 28  ⋅ 4H 2 O (50 μg/ml), while the Escherichia coli growth was of 12.93×10 7 ±0.25 CFU/ml at (NH 4 ) 2 [Ni(H 2 O) 6 ] 2 V 10 O 28  ⋅ 4H 2 O (5 μg/ml). This is in contrast to chloramphenicol (5 μg/ml) that allowed for Escherichia coli growth of 13.97×10 7 ±0.24 CFU/ml (control=17.33×10 7 ±0.48 CFU/ml).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

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