Solubilizing the thallium-platinum unit of Tl2Pt(CN)4. Preparation and use of a new crown ether/phosphine hybrid ligand for linking main-group and transition-metal ions

1990 ◽  
Vol 112 (16) ◽  
pp. 6139-6140 ◽  
Author(s):  
Alan L. Balch ◽  
Steven P. Rowley
MRS Advances ◽  
2020 ◽  
Vol 5 (17) ◽  
pp. 907-915 ◽  
Author(s):  
Jessica L. Sargent ◽  
Xunkai Chen ◽  
Mitchell C. Brezina ◽  
Sebastian Aldwin ◽  
John A. Howarter ◽  
...  

ABSTRACTIonic hydrogels are an abundant class of materials with applications ranging from drug delivery devices to high performance concrete to baby diapers. A more thorough understanding of interactions between polyelectrolyte networks and ionic solutes is critical as these materials are further tailored for performance applications in highly targeted ionic environments. In this work, we seek to develop structure-property relationships between polyelectrolyte gels and environments containing high concentrations of multivalent ions. Specifically, this work seeks to elucidate the causes behind differences in hydrogel response to divalent ions of main group metals versus transition metals. PANa-co-PAM hydrogels containing low and high fractions of ionic groups are investigated in solutions of DI water, NaCl, CaCl2, and CuSO4 at concentrations ranging from 5 to 100 mM in order to understand 1) the transient or permanent nature of crosslinks produced in these networks by divalent counter-ions, 2) the role of polymer ionic content in these interactions, and 3) how these interactions scale with salt concentration. Gravimetric swelling and mechanical compression testing are employed to characterize water and salt-swollen hydrogels in order to develop guiding principles to control and manipulate material properties through polymer-counter-ion interactions. The work presented here confirms the formation of permanent crosslinks by transition metal ions, offers explanation for the behavioral discrepancy observed between ionic hydrogels and main group versus transition metal ions, and illustrates how such hydrogel properties scale with counter-ion concentration.


2003 ◽  
Vol 101 (15) ◽  
pp. 2451-2467 ◽  
Author(s):  
PHILIP GEORGE ◽  
JENNY P. GLUSKER ◽  
GEORGE D. MARKHAM ◽  
MENDEL TRACHTMAN ◽  
CHARLES W. BOCK

2002 ◽  
Vol 339 ◽  
pp. 532-542 ◽  
Author(s):  
Jean Michel Grevy ◽  
Fabiola Tellez ◽  
Sylvain Bernés ◽  
Heinrich Nöth ◽  
Rosalinda Contreras ◽  
...  

Polyhedron ◽  
2004 ◽  
Vol 23 (8) ◽  
pp. 1461-1466 ◽  
Author(s):  
Qian-Ling Guo ◽  
Wen-Xiang Zhu ◽  
Shu-Lan Ma ◽  
Shu-Jing Dong ◽  
Miao-Qiong Xu

Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

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.


Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb

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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