2015
DOI: 10.13005/ojc/320228
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, Characterization and Antibacterial Activity of New Complexes of Some Lanthanide Ions with 15-Crown-5 and 18-Crown-6

Abstract: Complexes of some lanthanide picrates (Ln 3+ = Pr 3+, Nd 3+ and Dy 3+ ) with 15-crown-5 and 18-crown-6 were synthesized and characterized by elemental analysis, ICP-AES, FTIR, 1 H-NMR, 13C-NMR and UV-Visible spectrophotometric methods, thermal analysis (TGA & DTG), magnetic susceptibility , molar conductance and melting points. Also an in-vitro study on pathogenic gram positive (Staphylococcus aureus) and pathogenic gram negative bacteria (Escherichia coli, Salmonella and pseudomonas aeruginosa) was performed … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
3
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 9 publications
(4 citation statements)
references
References 22 publications
1
3
0
Order By: Relevance
“…The metal-ligand stoichiometry affects the oscillator strength; higher the value of oscillator strength, higher will be complexation and covalency. This is in an agreement with earlier findings [15][16][17][18] V. Table-3 Computed values of Judd-OfeltParameter (T λ ) for Er(III) complexes of CE, CB or CD (L 1 ) with AL, GY or AR (L 2 ), respectively, in 1:3:2 stoichiometry.…”
Section: Bonding Parameters 1) Nephelauxetic Ratio (β):Iner (Iii) supporting
confidence: 90%
“…The metal-ligand stoichiometry affects the oscillator strength; higher the value of oscillator strength, higher will be complexation and covalency. This is in an agreement with earlier findings [15][16][17][18] V. Table-3 Computed values of Judd-OfeltParameter (T λ ) for Er(III) complexes of CE, CB or CD (L 1 ) with AL, GY or AR (L 2 ), respectively, in 1:3:2 stoichiometry.…”
Section: Bonding Parameters 1) Nephelauxetic Ratio (β):Iner (Iii) supporting
confidence: 90%
“…Based on IR analysis of (CNTs‐ILC)/Crown and 18‐crown‐6 spectra (Figures A & B), the band of the (C−O−C) stretching vibration which is the most important band of the 18‐crown‐6 is observed in (CNTs‐ILC)/Crown spectrum as strong peak at 1107.9 cm −1 Figure A. This peak is assigned to the ether functional group (C−O−C) as it lies in the range 1110–1250 cm −1 . It indicates that crown ether was successfully deposited onto the surface of the CNTs‐ILC.…”
Section: Resultsmentioning
confidence: 96%
“…1A and 1B), which was assigned to the ether functional group (C-O-C) stretching vibration band. 49 Other peaks appeared at 1469 cm −1 and 1737 cm −1 for MWCNTs vibrational modes 50 and at 841 cm −1 and 558 cm −1 for C-N stretching vibrations of piperidinium core of ILC. 29 Scanning electron microscopy was used for examining the morphology of GC /CNT+ILC surface (Figure 1C), where a dense compact network structure of the (CNT+ILC) composite surface was observed.…”
Section: Methodsmentioning
confidence: 96%