Thermodynamical study on the formation of some mixed ligand complexes of non-transition metal ions in solution I. The formation and the stability of some Pb(II) mixed ligand complexes

2010 ◽  
Vol 9 (5) ◽  
pp. 415-420 ◽  
Author(s):  
Qi-Tao Liu ◽  
Feng Zhang ◽  
Xi-Ming Song ◽  
En-Jun Gao
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Mixed Ligand ◽  
Mixed Ligand Complexes ◽  
The Stability

Synthesis, Spectral and Antimicrobial Investigation of 2-(Naphthalenel-ylamino)-2- Phenylacetonitrile and 1, 10-Phenanthroline with Five Divalent Transition Metal Ions

2019 ◽  
Vol 10 (01) ◽  
Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Mixed Ligand ◽  
Gram Negative Bacteria ◽  
Magnetic Studies ◽  
Gram Positive Bacteria

Five new mixed ligand metal complexes have been synthesized by the reaction of divalent transition metal ions (Hg, Ni, Zn, Cu and Cd) with 2-(naphthalen-l-ylamino)-2-phenylacetonitrile (L1 ) and 1,10-phenanthroline (L2). The coordination likelihood of the two ligands toward metal ions has been suggested in the light of elemental analysis, UV-Vis spectra, FTIR, 1H-NMR, flam atomic absorption, molar conductance and magnetic studies. Results data suggest that the octahedral geometry for all the prepared complexes. Antibacterial examination of synthesized complexes in vitro was performed against four bacterias. Firstly, Gram-negative bacteria namely, Pseudomonas aerugin and Escherichia. Secondly, Gram-positive bacteria namely, Bacillus subtilis, Staphylococcuaurouss. Results data exhibit that the synthesized complexes exhibited more biological activity than tetracycline pharmaceutical.

scholarly journals Mixed Ligand Complexes of Transition Metal Ions with Selective Bio-Ligands in Surfactant-Water Mixtures

2019 ◽  
Vol 8 (2S11) ◽  
pp. 3182-3190
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Metal Ions ◽  
Chemical Speciation ◽  
Transition Metal Ions ◽  
Ternary Complexes ◽  
Mixed Ligand ◽  
Stacking Interactions ◽  
Micellar Media ◽  
Chelate Effect

Chemical speciation of ternary complexes of L-arginine and L-aspartic acid with essential transition metal ions was studied pH metrically. The following MLX, MLXH and ML2X ternary species are detected and reported in this paper. The existence of different ternary species is established from modeling studies using the computer program MINIQUAD75. The relative concentrations (M: L: X=1:2:2, 1:2:4, 1:4:2) and stabilities of the ternary species are compared with those of binary species. The extra stability associated with the ternary complexes is attributed to factors such as charge neutralization, chelate effect, stacking interactions and hydrogen bonding. Trend in variation of stability constants with the change in the mole fraction of the surfactant in various micellar media is explained on the basis of electrostatic and non-electrostatic forces. Distribution diagrams in relation to pH and plausible structures were presented.

scholarly journals Modification on Synthesis of Mixed Ligand Chelates by Using Di- and Trivalent Transition Metal Ions with Schiff Base as Primary Ligand

2014 ◽  
Vol 04 (03) ◽  
pp. 103-110 ◽  
Author(s):  
Abdussalam Ali Maihub ◽  
Faten Suliman Alassbaly ◽  
Marei Mailoud El-Ajaily ◽  
Abdunnaser Mohamed Etorki
Keyword(s):  
Schiff Base ◽  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Mixed Ligand

Metal Complexes of 6-Hydroxymethylpyridine-2-carboxylic Acid

1962 ◽  
Vol 15 (4) ◽  
pp. 786 ◽  
Author(s):  
RW Green ◽  
GKS Ooi
Keyword(s):  
Carboxylic Acid ◽  
Transition Metal ◽  
Metal Ions ◽  
Metal Complexes ◽  
Stability Constants ◽  
Steric Hindrance ◽  
Transition Metal Ions ◽  
Complexing Agent ◽  
Ph Titration ◽  
The Stability

Spectrophotometric and pH-titration methods have been used to determine the stability constants at 25 �C of complexes between transition metal ions and the anion of 6-hydroxymethylpyridine-2-carboxylic acid. This anion is found to be a weaker base and a weaker complexing agent than the pyridine-2-carboxylate ion. There is some evidence for steric hindrance of tris complexes.

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