Search results for "Solid-state"
showing 10 items of 530 documents
Syntheses and structure of bis(pentamethylcyclopentadienyl)dithiophosphinato complexes
1997
Bis(pentamethylcyclopentadienyl)phosphane Cp*2PH reacts with sulfur under basic conditions to give the corresponding dithiophosphinate salts M+ CP*2PS−2 (5 M+ = HNEt+3, 6 M+ = Li+), which are formed via the intermediate CP*2P(S)H (4). Both salts on treatment with cobalt(II) chloride give rise to the transition metal dithiophosphinate 7. The structures of this new type of diorganodithiophosphinate complexes in the solid state have been investigated. © 1997 John Wiley & Sons, Inc. Heteroatom Chem 8: 521–525, 1997
Synthesis and Characterisation of Chiral Triazole-Based Halogen-Bond Donors: Halogen Bonds in the Solid State and in Solution
2017
A general platform for the synthesis of various chiral halogen-bond (XB) donors based on the triazole core and the characterisation of factors that influence the strength of the halogen bond in the solid state and in solution are reported. The characterisation of XB donors in the solid state by X-ray crystallography and in solution by 1H NMR titration can be used to aid the design of new XB donors. We describe the first example of a XB between iodotriazoles and thioureas in solution. In addition, the enantiodiscrimination of acceptors in solution through halogen-bond participation is described.
Adsorbents and columns in analytical high-performance liquid chromatography: A perspective with regard to development and understanding
2012
A brief historical survey is presented on the evaluation of silica adsorbents in analytical HPLC. The theory of analytical HPLC is mostly still being based on the height equivalent to a theoretical plate concept and the van Deemter equation that was derived from gas phase adsorption involving a linear adsorption isotherm and fast mass transfer kinetics. One can obviously wonder whether the use of the van Deemter equation is relevant and valid for the evaluation of the performance of HPLC systems, where most often the liquid solutes involve charged molecules in electrolytes and in very many cases the adsorbates are macromolecules having diffusion coefficients of small magnitude. Instead of t…
Friction Based Solid State Welding Processes
2012
In the last decade the industrial use of solid state welding processes based on frictional forces work decaying into heat is continuously increasing due to their strong advantages with respect to traditional fusion techniques. Several advances have been proposed by the scientific community regarding process mechanics, material flow and also the computer aided engineering of the operation with the aim to maximize the mechanical performances of the welded joints. In the paper Friction Stir Welding (FSW) and Linear Friction Welding (LFW) operations are considered and a review of the most relevant research issues and results is provided.
Magnetic Ion Exchange Interactions in NiO—MgO Solid Solutions
2006
In this work, a review of recent experimental data and their interpretation for NicMg1−c O solid solutions is given. In particular, the influence of exchange interactions between Ni2+ ions on the structural, optical, magnetic, and vibrational properties is discussed.
Phenylene motion in polycarbonate and polycarbonate/additive mixtures
1987
Pulsed deuteron NMR line shapes have been analysed to characterize type and time scale of the phenylene group motion in glassy bisphenol-A polycarbonate. The motional mechanism involvesπ-flips about theC1C4 axis augmented by small angle fulctuations about the same axis, reaching a rms amplitude of ±35‡ at 380 K. The distribution of correlation times for theπ-flips is heterogeneous in nature and can be described either by a log-Gaussian or an asymmetric distribution with a more rapid decay at high correlation times comparable to the Williams-Watts distribution. From both distributions essentailly the same mean activation energy of 37 kJ/mol is obtained, whereas the temperature dependent widt…
The polarization dependence of x‐ray photoelectron yield of a Au photocathode
1994
We report a measurement of the total photoelectron yield of gold as a function of the incident x‐ray polarization. Polarized x rays with energies of 2.5, 2.7, and 4.0 keV were used to excite a gold photocathode at a glancing incidence angle between 5° and 50°. Contrary to a previous report, we found no measurable polarization dependence for all three x‐ray energies. We conclude that the modulation factor, i.e., the fractional change of the total yield when the polarization state is varied, is less than 4%.
Inclusion complexes of cyclomaltooligosaccharides (cyclodextrins) with melatonin in solid phase
2005
Fourier transform infrared spectrometry (FT-IR) and X-Ray diffraction (XRD) investigations were carried out on MLT plus α-, β- and γ-CD physical mixtures and lyophilized or crystalline MLT/α-, β-, γ-CD complexes. Inclusion complexes formation between MLT and cyclodextrins in solid phase has been emphasized by the significant differences between IR and XRD spectra of physical mixtures with respect to those of the complexes. The structure of MLT CDs complexes in the solid state as well as the biochemical and pharmaceutical implications are discussed.
Piranilidena atvasinājumu optiskās un pastiprinātas spontānās emisijas īpašības PVK matricā
2015
Organiskie materiāli ir daudzsološi dažādiem moderniem pielietojumiem, tai skaitā optiski ierosinātiem organiskajiem cietvielu lāzeriem, kuriem vajadzīgi materiāli ar augstu pastiprināšanās koeficientu un zemām ierosmes enerģijām. Vairumā organisko sistēmu šie parametri ir limitēti krāsvielu molekulu kristalizācijas dēļ. Tādēļ savienojumi ar samazinātu kristalizēšanos būtu ļoti noderīgi. Šajā darbā tika pētītas plānās kārtiņas ar jauniem plaši zināmās krāsvielas DCM atvasinājumiem PVK polimēra matricā dažādās koncentrācijās. Kārtiņām tika uzņemti fotoluminiscences spektri un veikti pastiprinātas spontānās emisijas (PSE) mērījumi. Tika novērota spēcīga koncentrācijas ietekme uz emisijas spek…
Solution and solid-state studies on the halide binding affinity of perfluorophenyl-armed uranyl–salophen receptors enhanced by anion–π Interactions
2016
The enhancement of the binding between halide anions and a Lewis acidic uranyl-salophen receptor has been achieved by the introduction of pendant electron- deficient arene units into the receptor skeleton. The association and the occurrence of the elusive anion-p interaction with halide anions (as tetrabutylammonium salts) have been demonstrated in solution and in the solid state, providing unambiguous evidence on the interplay of the concerted interactions responsible for the anion binding.