Conversion of endohedral <Superscript>133</Superscript>Xe-fullerene to endohedral <Superscript>133</Superscript>Xe-fullerenol to be used in nuclear medicine

Summary Hydrophilic endohedral ¹³³Xe-fullerenols, [¹³³Xe@C₆₀(OH)_xand ¹³³Xe@C₇₀(OH)_x], were synthesized from hydrophobic endohedral ¹³³Xe-fullerenes. The yield of endohedral ¹³³Xe-fullerenols extracted in water was about 40% and 23% for C₆₀and C₇₀, respectively. The products stored in 0.9% NaCl solution at 20 °C were stable enough to be used in nuclear medicine.     

An application of silaned glass beads to the preconcentration and spectrophotometric determination of traces of phosphorus with molybdate

Silaned glass beads are applied to the preconcentration and spectrophotometric determination of phosphorus as the phosphomolybdenum blue complex. Traces of phosphorus in water are collected as a phosphomolybdenum blue complex on a column of the beads. The phosphomolybdenum blue is eluted with N,N-dimethylformamide and the absorbance of the eluate continuously monitored at 700 nm. The height of the very sharp peak obtained is proportional to the amount of phosphorus present and 0.1-0.5 mug of phosphorus in a 10-ml sample can be determined reproducibly. Interference from arsenate is eliminated by addition of a reducing agent. High concentrations of silica cause a small positive error. This method is applicable to the analysis of river water and sea-water samples.     

Comparison of quantitative methods for analysis of polyphasic pharmaceuticals

Adequate very sensitive quantification methods are needed for the development and are also now required for the monitoring of undesirable solid form(s) as routine tests. The pre-requisite for quantitation are selectivity, sensitivity and most important the purity of standards and their proper storage, what is a challenge for metastable forms. Several analytical techniques are available such as X-ray diffraction, spectroscopy, thermal analysis and microcalorimetry. The different steps of the validation of the analytical methods and problems to be solved are discussed. Examples illustrate the different techniques and compare their possible advantages and limits. The relative standard deviation of measurements should allow for checking the homogenization procedure of mixtures for calibration. The validation should be carried out following ICH guidelines for validation of analytical methods. Comparison of different techniques in adequate concentration range add confidence in the analytical results.     

Temperature influence on hydrogen sorption in palladium limited-volume electrodes (Pd-LVE)

The effect of temperature on hydrogen and deuterium electrosorption into a palladium LVE (limited-volume electrode) has been investigated. A decrease in hydrogen capacity (H/Pd ratio) with increasing temperature has been observed. Temperature strongly influences the plots of measured H(D)/Pd values vs. potential scan rate. In addition, hydrogen absorption was found to be dependent on the composition of the surrounding electrolyte solution. These results have confirmed the hypothesis that two different mechanisms of hydrogen desorption from the palladium electrode take place, namely electrochemical oxidation and non-electrochemical recombination. Further, the ratio between the rate constants for these two processes has been found to change with temperature. Electronic Publication     

Kinetics of thermal decomposition of alkaline phosphates

Summary The thermal behavior of KH₂PO₄, NaH₂PO₄ and Na₂HPO₄ under non-isothermal conditions using TG method with different heating rates was studied. The values of the reaction rate were processed by means of Friedmans differential-isoconversional method. A dependence of the activation energy vs. conversion was observed. Therefore a procedure based on the compensation effect (suggested by Budrugeac and Segal) was applied. A less speculative data processing protocol was offered by the non-parametric kinetics method suggested by Serra, Nomen and Sempere. Three steps were observed by non-isothermal heating: a dehydration, a dimerization and a polycondensation. The differences in the intimate reaction mechanism are determined by the initial number of water molecules.     

Interaction of gas phase atomic hydrogen with Pt(111):Direct evidence for the formation of bulk hydrogen species

Employing hot tungsten filament to thermal dissociate molecular hydrogen,we generated gas phase atomic hydrogen under ultra-high vacuum(UHV)conditions and investigated its interaction with Pt(111) surface.Thermal desorption spectroscopy(TDS)results demonstrate that adsorption of molecular hy- drogen on Pt(111)forms surface Had species whereas adsorption of atomic hydrogen forms not only surface Had species but also bulk Had species.Bulk Had species is more thermal-unstable than surface Had species on Pt(111),suggesting that bulk Had species is more energetic.This kind of weakly- adsorbed bulk Had species might be the active hydrogen species in the Pt-catalyzed hydrogenation reactions.     

Selective growth of ag nanowires on Si(111) surfaces by electroless deposition

Electroless deposition of Ag on atomically flat H-terminated Si(111) surfaces in aqueous alkaline solutions containing Ag ions produced two different sizes of Ag nanowires along atomic step edges: (1) a narrow nanowire of 10 nm in width and 0.5 nm in height and (2) a wide nanowire of 35 nm in width and 11 nm in height. The narrow and wide nanowires were formed by immersion in the solutions containing less than 1 ppb and 8 ppm dissolved-oxygen concentrations, respectively. This result indicates that the dissolved oxygen initiates the formation of Ag nucleation sites and that the fabrication method has a possibility of controlling the size of Ag nanowires.     

An Easy One-Pot Procedure for the Synthesis of <Emphasis Type="Italic">N</Emphasis>-Sulfonyl Phosphorous Ylides and Sulfonyl Iminophosphoranes

Summary. Reaction of triphenylphosphine and an electron deficient acetylenic ester in the presence of strong N–H acid such as alkyl and aryl sulfamides or acetamide produces phosphorous ylides at room temperature in CH₂Cl₂. The aryl sulfamide phosphoranes undergo a smooth transformation reaction in boiling toluene and produce iminophosphoranes.     

Synthesis of multisubstituted 1,3-butadienes using the ruthenium-catalysed double addition of trimethylsilyldiazomethane to alkynylboronates

The ruthenium-catalysed double addition of trimethylsilyldiazomethane to alkynes developed by Dixneuf and co-workers was applied to the synthesis of 2-alkyl- or 2-aryl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-bis(trimethylsilyl)-1,3-butadienes by use of alkynylboronates instead of alkynes. Di- and tetrasubstituted 1,3-butadienes were prepared from a 2-boryl-1,4-disilyl-1,3-butadiene, using the Suzuki-Miyaura coupling reaction, iodolysis of the alkenylsilane moieties with N-iodosuccinimide and hydrolysis of the carbon-silicon bonds with trifluoroacetic acid. The same compound was converted also to a bicyclic compound, a trisubstituted 1,3-butadiene and a dienone through the Diels-Alder reaction, oxidation of the alkenylboronate moiety and the Mukaiyama aldol reaction.