Search results for "Stoichiometry"
showing 10 items of 270 documents
Spectrophotometric study on the thermodynamics of binding of α- and β-cyclodextrin towards some p-nitrobenzene derivativesElectronic supplementary in…
2003
Binding properties of native α- and β-cyclodextrin towards some nitrobenzene derivatives have been studied by means of UV-vis spectrophotometry. The former host is able to form complexes having 1 : 1 and 1 : 2 stoichiometric ratios with these guests, while only 1 : 1 complexes are detected with the latter host. A careful analysis of the thermodynamic parameters for complexation equilibria, under the perspective of the enthalpy–entropy compensation effect, reveals that binding abilities of the two different hosts are subject to different features.
The role of potassium and hydrogen ions in the Prussian Blue ⇆ Everitt's Salt process
1998
Cyclic voltammetry experiments have proved very useful in the knowledge and understanding of the role of the potassium and hydrogen ions during the Prussian Blue ⇄ Everitt's Salt process. While potassium ions act as a stoichiometric reactant, the hydrogen ions play a very important role in the kinetics of the electron-hopping process. The entropy change for the reaction PB ⇄ ES has proved to be dependent on the degree of crystallinity of the film, indicating that this entropy change is related to the fixation of inner counterions on the crystal structure of the films.
Discrete bond model (DBM) of sodium silicate glasses derived from XPS, Raman and NMR measurements
1993
In sodium silicate glasses, the fraction of differently bound Si species Q[i] (i = 0−4), depending on the number i of bridging oxygens bound to the quarternary silicon, is a function of stoichiometry and the Na/Si ratio. Sodium silicate glasses were investigated by high resolution X-ray photoelectron spectroscopy. To explain the differences in chemical shifts and linewidths of the O 1s signal of the bridging and the non-bridging oxygen as a function of alkali concentration, and extended glass model was developed. This new model takes into account the influence of the alkali concentration on the Q[i] distribution and on the appearance and concentrations of differently bound bridging oxygens …
A new improved synthesis of the 110 K bismuth superconducting phase: freeze-drying of acetic solutions
1992
Abstract Metastability has greatly hindered the separated synthesis of the high-temperature superconducting phases represented as (Bi1−x, Pbx)2Sr2Can−1CunO4 + 2n (n = 2, 2-2-1-2, Tc≈80 K, and n = 3, 2-2-2-3, Tc≈110 K). By careful control of the synthetic variables, it becomes possible to obtain the 110 K phase as the only superconducting one through processing of freeze-dried acetic solutions. This technique leads to homogeneously sized (5–10 μm) micaceous platelets of the superconducting material.
Self-Assembled Polymers Based on bis-Tetra-Urea Calix[4]arenes Connected via the Wide Rim
2008
Six double calixarenes were synthesised in which two tetra-urea calix[4]arenes are linked by a rigid spacer between the urea functions at their wide rim. The dimerisation of their tetra-urea parts leads to hydrogen-bonded polymeric assemblies in apolar solvents. The addition of the stoichiometric amount of a tetra-tosylurea calix[4]arene disrupts the polymeric structures due to the preferred formation of heterodimeric capsules between tetra-aryl and tetra-tosylurea calix[4]arenes. The existence of polymeric assemblies was further established by AFM studies on spin-coated samples.
X-Ray Scattering Studies of Organic Monolayers on Electrolytic Solutions: Arachidic Acid on CdCl2
1992
The interaction between a charged monolayer of fatty acid molecules on the surface of a CdCl2 aqueous solution and the ions below has been investigated by means of X-ray Reflection and Grazing-Incidence Diffraction. A stoichiometric, localised layer of Cd++ ions forms an epitaxial 2×3 superstructure below the 2D-crystalline fatty acid monolayer.
Spectroscopic behaviour of metal–drug complexes. Infrared spectra of Cu(II) complexes with 5-amino-1,3,4-thiadiazole-2-thiol (Hatm)
1997
Abstract The infrared spectra of the drug Hatm and its copper (II) complexes with stoichiometry [Cu(atm) 2 (H 2 O)] and [Cu(Hatm)(HIm) 2 (SO 4 )] are reported and discussed. The Raman spectrum of Hatm is also reported. An assignment of Hatm, HIm, H 2 O and SO 4 modes in the complexes is proposed in comparison with the modes of the free ligands. Important information about the metal–ligand vibrations has been obtained.
Microwave-assisted synthesis of novel cyclodextrin–cucurbituril complexes
2011
Microwave irradiation was successfully used in order to obtain stable supramolecular aggregates between cyclodextrins and cucurbiturils, without the participation of any long-chain common ‘molecular thread’ guest. These aggregates were characterised by means of various different techniques, namely NMR, thermogravimetry, polarimetry and ESI-MS. Cross-analysis of experimental data allowed us to obtain insights on the stoichiometries of the composites and their thermal stabilities. The possible structures of the composites are briefly discussed, as well as the actual nature of their intrinsic stability.
Properties of Multi Phase Interfaces on the Tungsten Trioxide Particles in the Thin Films
2000
A wide spectrum of physical and chemical properties of thin films of tungsten trioxide compounds depend on composition, constitution and structure of the film, interaction with environment, and the type of external influences/excitations. The reason is the non-stoichiometric nature of transition metal oxides and properties of d-electrons. The short range order of non-stoichiometric compounds or phases of WO3 has a strong perovskite arrangement of tungsten and oxygen ions [1, 2]. The smallest crystalline clusters of perovskite short range order consist 6÷9 of [WO6]-octahedrons. One of the structural peculiarities-features of tungsten trioxide, related to non-stoichiometry, is a variety of [W…
ChemInform Abstract: One-Pot Synthesis of Pyrrole-2-carboxylates and -carboxamides via an Electrocyclization/Oxidation Sequence.
2015
An electrocyclic ring closure is the key step of an efficient one-pot method for the synthesis of pyrrole-2-carboxylates and -carboxamides from chalcones and glycine esters or amides. The 3,4-dihydro-2H-pyrrole intermediates generated in situ are oxidized to the corresponding pyrroles by stoichiometric oxidants or by catalytic copper(II) and air in moderate to high yields. A wide range of functional groups are tolerated, and further combination with an in situ bromination gives access to polyfunctional pyrrole scaffolds.