Complexation of polymer-bound imino diacetate-type chelating agents with some transition-metal ions. Effect of charged polymer chains on chelate formation reactions

1988 ◽  
Vol 84 (3) ◽  
pp. 841 ◽  
Author(s):  
Yoshimi Kurimura ◽  
Kiyomi Takato
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Chelating Agents ◽  
Transition Metal Ions ◽  
Polymer Chains ◽  
Chelate Formation ◽  
Charged Polymer

Competition between Cd(II) and other divalent transition metal ions during complex formation with amino acids, peptides, and chelating agents

2016 ◽  
Vol 327-328 ◽  
pp. 55-69 ◽  
Author(s):  
Maurizio Remelli ◽  
Valeria M. Nurchi ◽  
Joanna I. Lachowicz ◽  
Serenella Medici ◽  
M. Antonietta Zoroddu ◽  
...  
Keyword(s):  
Amino Acids ◽  
Complex Formation ◽  
Transition Metal ◽  
Metal Ions ◽  
Chelating Agents ◽  
Transition Metal Ions

o-hydroxyaroyl-isonicotinoyl hydrazones as chelating agents with divalent transition metal ions

1994 ◽  
Vol 19 (3) ◽  
Author(s):  
RamadanM. El-Bahnasawy ◽  
SomiaE. El-Meleigy ◽  
Abd-Alla El-Tawansi
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Chelating Agents ◽  
Transition Metal Ions

The N-acylhydrazine grouping as a ligand. I. Coordination compounds of Keto- and Enol-N-acylhydrazines with cobalt(II), nickel(II), and copper(II)

1972 ◽  
Vol 25 (2) ◽  
pp. 289 ◽  
Author(s):  
JF Alcock ◽  
RJ Baker ◽  
AA Diamantis
Keyword(s):  
Complex Formation ◽  
Transition Metal ◽  
Metal Ions ◽  
Coordination Compounds ◽  
Chelating Agents ◽  
Transition Metal Ions ◽  
Enol Form ◽  
Oxidation States ◽  
Keto Form ◽  
Formation Of Complexes

Ligands containing the N-acylhydrazine grouping, RCONHKH2, act as bidentate chelating agents with transition metal ions. Cationic complexes of coba1t(11), nickel(11), and copper(11) containing the ligands coordinated in the keto form were isolated, but the ligands also reacted in the enol form producing neutral complexes with cobalt(111) and copper(11). Complex formation in the enol form was facilitated by condensation of the ligands with acetone to produce the N'-iso-propylidene derivatives, from which keto complexes were also isolated. Under certain conditions N-acylhydrazines can act as reducing agents, leading to the formation of complexes containing copper in both oxidation states (I) and (11). Using N-benzoylhydrazine, this reaction can be utilized as a benzoylating medium for amines.

Subcomponent self-assembly of polymer chains based on dynamic and geometrical coordination diversity of the first row transition metal ions

2014 ◽  
Vol 5 (4) ◽  
pp. 1202-1209 ◽  
Author(s):  
Xuewen Wu ◽  
Na Xu ◽  
Zhengguang Zhu ◽  
Yuanli Cai ◽  
Ying Zhao ◽  
...  
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Self Assembly ◽  
Transition Metal Ions ◽  
Polymer Chains

HREM Study of electron-induced surface radiation damage in ReO3

1991 ◽  
Vol 49 ◽  
pp. 636-637
Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Metal Oxides ◽  
Electron Irradiation ◽  
Transition Metal Oxides ◽  
Carbon Film ◽  
Transition Metal Ions ◽  
Surface Radiation ◽  
Valence Transition ◽  
Electron Microscopes

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.

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.

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