Isomorphous Substitution of Transition-Metal Ions in the Nanoporous Nickel Phosphate VSB-5

2005 ◽  
Vol 109 (2) ◽  
pp. 845-850 ◽  
Author(s):  
Sung Hwa Jhung ◽  
Jong-San Chang ◽  
Young Kyu Hwang ◽  
Jean-Marc Grenèche ◽  
Gérard Férey ◽  
...  
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Isomorphous Substitution ◽  
Nickel Phosphate

Transition Metal Ions in Microporous Crystalline Aluminophosphates: Isomorphous Substitution

1999 ◽  
Vol 1999 (4) ◽  
pp. 565-577 ◽  
Author(s):  
Bert M. Weckhuysen ◽  
R. Ramachandra Rao ◽  
Johan A. Martens ◽  
Robert A. Schoonheydt
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Isomorphous Substitution

ChemInform Abstract: Transition Metal Ions in Microporous Crystalline Aluminophosphates: Isomorphous Substitution

ChemInform ◽  
2010 ◽  
Vol 30 (19) ◽  
pp. no-no
Author(s):  
Bert M. Weckhuysen ◽  
R. Ramachandra Rao ◽  
Johan A. Martens ◽  
Robert A. Schoonheydt
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Isomorphous Substitution

scholarly journals Open-framework aluminophosphates: Synthesis, characterization and transition metal modifications

2005 ◽  
Vol 70 (3) ◽  
pp. 371-391 ◽  
Author(s):  
Nevenka Rajic
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Active Sites ◽  
Transition Metal Ions ◽  
Isomorphous Substitution ◽  
Synthesis Conditions ◽  
Open Framework ◽  
Wide Range ◽  
Redox Ability ◽  
Compositional Diversity

This review is a brief summary of open-framework aluminophosphates and their transition metal-substituted modifications. The materials exhibit structural and compositional diversity, as well as a wide range of pore openings, which are crystallographically ordered and can be tuned by an appropriate choice of synthesis conditions. The diameters of the apertures, cages and channels fall in the range of 0.4 to about 1.5 nm, which recommends aluminophosphates for a novel area of application-nanocatalysis. Isomorphous substitution of the framework elements by transition metal ions which possess redox ability creates active sites inside the aluminophosphate lattice and opens routes towards shape selective bi-functional catalysis. In order to obtain an insight into the location of the transition metal ions, different characterization techniques have to be used.

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.

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.

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