Search results for "visual_art"
showing 10 items of 2987 documents
Cytochemical techniques for zinc and heavy metals localization in nerve cells
2002
Zinc is one of the most abundant oligoelements in the living cell. It appears tightly bound to metallothioneins, loosely bound to some metalloproteins and nucleic acids, or even as free ion. Small amounts of zinc ions (in the nanomolar range) regulate a plentitude of enzymatic proteins, receptors, and transcription factors; thus, cells need accurate homeostasis of zinc ions. Some neurons have developed mechanisms to accumulate zinc in specific membrane compartments ("vesicular zinc") which can be revealed using histochemical techniques. This article is a short report on the different direct-indirect experimental approaches for zinc and heavy metal detection in neurons. Substances giving a b…
The geometry of the silver 1,1′-dibenzyl-2,2′-biimidazole complexes
2013
Abstract The argentophilic interactions and interactions of weakly coordinated nitrate and water with silver metal were studied by investigating the reaction of 1,1′-dibenzyl-2,2′-biimidazole (Bn2bim) with silver nitrate. Three new silver complexes [Ag4(Bn2bim)4(NO3)2]·4(CH3CH2OH)·2(NO3)·0.5(H2O) (1), [Ag4(Bn2bim)4(H2O)4]·4(NO3) (2) and [Ag4(Bn2bim)4(NO3)4]·6(CH2Cl2)·2(H2O) (3) were synthesized and characterized. Complexes 1-3 have rare tetranuclear twisted closed cyclic structure with four bridging biimidazoles and variable nitrate/water ratio. The interactions between the nitrate ligand and Ag as well as water ligands and Ag are considered to be weak due to the ease of exchanging them. Th…
Mononuclear coordination compounds based on a novel chelating triazole ligand: 1-vinyl-3-acetylamino-1,2,4-triazole
2002
The synthesis, X-ray structure, magnetic and spectroscopic properties of new Co(II), Ni(II) and Cu(II) complexes with 1-vinyl-3-acetylamino-1,2,4-triazole (vaat) are reported. The crystal structures of [Ni(vaat)2(H2O)2](NO3)2 and [Cu(vaat)2(H2O)2]Cl2 have been determined by X-ray diffraction. In these mononuclear complexes, the metal ion is surrounded by two water molecules in axial positions and two oxygen and two nitrogen (N4) atoms coming from two trans-oriented chelating vaat molecules. Anions are noncoordinated and are involved in a hydrogen bonding network. The complex cations of [Cu(vaat)2(H2O)2]Cl2 are aligned within chains. In the structure of [Ni(vaat)2(H2O)2](NO3)2 the nitrate an…
Optical properties of different polymer thin films containing in situ synthesized Ag and Au nanoparticles
2009
Here we report on the in situ synthesis of Ag and Au nanoparticles inside several polymer matrixes by solid-state chemical reduction of a metallic salt. Poly(ethyleneimine) (PEI), poly(hydroxyethyl methacrylate) (PHEMA), poly(vinylpyrrolidone) (PVP), novolak, poly(4-vinylphenol) (P4VP), poly(4-vinylphenol)-co-(methyl methacrylate) (P4VP-co-MMA) and poly(styrene-co-allyl alcohol) (PS-co-AA) were able to reduce Ag(I) and Au(III) to the corresponding nanoparticles during the baking process. The nanoparticle diameters of Ag and Au were found to range from 2 to 25 nm. TEM also indicated a uniform distribution of nanoparticles embedded in the thin film. This approach is suitable for controlling t…
Divalent metal phosphonates – new aspects for syntheses, in situ characterization and structure solution
2016
Abstract Divalent metal phosphonates are promising hybrid materials with a broad field of application. The rich coordination chemistry of the phosphonate linkers enables the formation of structures with different dimensionalities ranging from isolated complexes and layered structures to porous frameworks incorporating various functionalities through the choice of the building blocks. In brief, metal phosphonates offer an interesting opportunity for the design of multifunctional materials. Here, we provide a short review on the class of divalent metal phosphonates discussing their syntheses, structures, and applications. We present the advantages of the recently introduced mechanochemical pa…
Evaporation of tungsten oxides: A mass-spectrometric study of the vapour contents
1995
Abstract The evaporation of bulk oxides of WO2 and WO3 and oxidised tungsten surfaces (metallic tungsten heated in an oxygen atmosphere) have been studied by the means of mass-spectrometry. The principal constituents of the vapour are found to be molecules of WO2, WO3, W2O6 and W3O9. These results differ from earlier reports, where the presence of molecules smaller than W3O9 in the mass-spectrum was interpreted as an artifact due to electron impact dissociation of larger polymers.
Model Pumices Supported Metal Catalysts
1997
The catalyzed, selective hydrogenation, in liquid phase, of 1,3-cyclooctadiene was studied on a series of Pd catalysts supported on natural pumice, model pumices (with variable content of alkali metal ions), silica, and sodium-doped silica. At constant pressure of H2(1 atm.) the reaction follows a zero-order kinetic for all the Pd catalysts. At low metal dispersion (Dx < 20%), Pd/pumice catalysts exhibit higher activity as compared to Pd/silica catalysts; the turnover frequency is maintained even at high metal dispersion in Pd/pumice but Pd/silica and Pd/model pumices without alkali ions show a decrease in activity. At increasingDx, the binding energy shift of Pd 3dlevel is negative in Pd/p…
Polymeric scaffolds prepared via Thermally Induced Phase Separation (TIPS): Tuning of structure and morphology
2007
Scaffolds suitable for tissue engineering applications were prepared by Thermally Induced Phase Separation (TIPS) starting from a ternary solution PLLA/dioxane/water. The experimental protocol consisted of three consecutive steps, a first quench from the homogeneous solution to an appropriate demixing temperature (within the metastable region), a holding stage for a given residence time and a final quench from the demixing temperature to a low temperature (within the unstable region). A large variety of morphologies, in terms of average pore size and interconnection, were obtained upon modifying the demixing time and temperature, owing to the interplay of nucleation and growth processes dur…
Coordination ability of pentapeptides with two dehydro-amino acid residues inserted into their sequences.
2004
The study on the binding ability of tested ligands have shown that insertion of two dehydro-amino acid residues into peptide sequences makes them more effective in metal ion binding than ligands with one dehydro-amino acid residue. The ligand with two Z(Delta)Phe residue form more stable complexes than his analogues with one Z(Delta)Phe residue. Interesting is this that position of Z(Delta)Phe residue in peptide chain have impact on Cu(II)-complexes formation.
Anion coordination chemistry in aqueous solution of polyammonium receptors
2006
The behavior of polyamines as receptors of selected families of anions in water is explored. First metallocyanide interaction with saturated polyammonium hosts is analyzed both in solution and in the solid state. The utility of potentiometry, multinuclear NMR, microcalorimetry and cyclic voltammetry to describe solution features of this chemistry is described for selected systems. Sulfate, phosphate, polyphosphate and nucleotide interactions with large polyammonium receptors are then reviewed. Hydrogen bond formation is discussed from a thermodynamic point of view. The influence of the presence of aromatic fragments within the structure on the binding strength is discussed. Factors affectin…