2020
DOI: 10.37628/jcscr.v6i1.950
|View full text |Cite
|
Sign up to set email alerts
|

Green Synthesis of Nickel(II) and Zinc(II) Complexes of Bis(Imine) Schiff base Derived from o-vanilline and m-phenylenediamine.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

2
4
0

Year Published

2022
2022
2023
2023

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(6 citation statements)
references
References 0 publications
2
4
0
Order By: Relevance
“…The bands at 456.00 cm -1 (758.39 cm -1 ) and 426.60 cm -1 (701.24 cm -1 ) which could not be traced in the spectrum of aspirin is tentatively assigned to M-O and M-Cl stretching frequencies as shown in the Table 4. These values were consistent with the results of [15]. The results as presented in Table 5 shows that aspirin is active against all the bacteria isolates in all concentrations except in E. coli at 500 μg, while the complexes from both methods showed an increase in the activity than the free ligand of aspirin and are compared with the standard of ciprofloxacin as reported by [16].…”
Section: Resultssupporting
confidence: 90%
See 1 more Smart Citation
“…The bands at 456.00 cm -1 (758.39 cm -1 ) and 426.60 cm -1 (701.24 cm -1 ) which could not be traced in the spectrum of aspirin is tentatively assigned to M-O and M-Cl stretching frequencies as shown in the Table 4. These values were consistent with the results of [15]. The results as presented in Table 5 shows that aspirin is active against all the bacteria isolates in all concentrations except in E. coli at 500 μg, while the complexes from both methods showed an increase in the activity than the free ligand of aspirin and are compared with the standard of ciprofloxacin as reported by [16].…”
Section: Resultssupporting
confidence: 90%
“…The IR data of the aspirin and its complexes are reported in Table 4. The IR data of metal complexes behaves as bidentate manner which coordinate via one of the oxygen atoms of acidic group with the displacement of hydrogen atom and carbon of ester [15], bands at 1752.46cm -1 and 1581.71 cm -1 in the spectrum of free aspirin are assigned to υ(C=O) by ester and carboxylic group after deprotonation as these shifted in different frequencies 1756.82 cm -1 (1577.68 cm -1 ) and 1756.54 cm -1 (1681.41 cm -1 ) for both methods. The shifted proves that these groups represent the coordination sites of aspirin after deprotonation in carboxylic group (Mustapha et al, 2014).…”
Section: Resultsmentioning
confidence: 99%
“…These higher values provide the evidence of coordination between the ligand and metal ions as reported by [7]. Conductivity measurement as shown in Table 1 and performed in 1x10 Similar results were reported by [10]. The electronic spectra data is shown in Table 4 in which the ligand present three distinct absorption bands at 207nm, 208nm and 238nm attributed to n-π * , π-π * and C T which was assigned to the metal-ligand charge transfer [11].…”
Section: Resultssupporting
confidence: 79%
“…Table 4 exhibits the results of an analysis of the IR spectral data comparing the bonding types that occur in complexes to those that occur with free HCBHDCS ligands. The free HCBHDCS ligand exhibits IR bands at 3216, 3190, and 1652 cm -1 for phenolic (C-O), (N-H), and (C=O), respectively [41][42][43]. The phenolic band was observed at 3216 cm -1 in the ligand; the absence of this band in complexes is evidence that the phenolic oxygen has been coordinated with metal ions via deprotonation [44].…”
Section: Ft(ir) Spectramentioning
confidence: 99%