Synthesis of tricyclic aromatic compounds by the intramolecular pauson-khand reaction promoted by molecular sieves(,)(1)

Pauson-Khand reactions are carried out with different substituted aromatic enynes, yielding tricyclic cyclopentenones related to natural products such as chromenes. Enynes are easily obtained in a two-step approximation from the corresponding salicylaldehydes. The reaction is promoted by dissolved TMANO (trimethylamine N-oxide) and/or 4 A molecular sieves. This new way of induction for the Pauson-Khand reaction increases yields remarkably, allowing the reaction of some substituted alkenes which fail to react in the absence of the zeolite. Isomerization of the double bond of the cyclopentenone ring is observed except when nonterminal triple bonds are used. For trisubstituted alkenes, an interrupted Pauson-Khand process is observed with moderate yields.     

QCD Calculation ofK0 - [`(K)]0K^0 - \bar K^0 mixing from three-point function sum rules

We calculate theB parameter for mixing in the framework of QCD sum rules for a three-point function involving pseudoscalar currents, and contrast our results with other calculations. We findB=0.5±0.1±0.2, where the first error reflects uncertainties in the various QCD parameters and the second one is an estimate of uncalculated three-loop radiative and higher order quark mass corrections.     

Numerical Analysis of the Behaviour of Tooth Intrarradial Posts by the Finite Element Method

The aim of this work is to study the behaviour of a carbon/epoxi post housed in a canine tooth after endodontic treatment in order to support the typical loads present during mastication. The three-D basic design of the dental piece consisting of tooth + post was carried out with a three-dimensional parametric design program. We study the stresses and displacements of the different elements of the dental piece under normal load conditions, and present the results and conclusions.     

Spectroscopic study of the aluminium/lumogallion system in the presence of non-ionic surfactants

The effects of different non-ionic ethylene oxide condensate surfactants on the fluorescence and the molecular absorption of the aluminium/lumogallion system are reported. Ethylene oxide condensates with fatty alcohols give higher micellar enhancement factors than tert-octylphenols or nonylphenols; ethylene oxide/propylene oxide copolymers provide only a 50% increase in the fluorescence of the complex. The aluminium/lumogallion seems to form mixed micelles with the fatty alcohol condensates; the strong complex/micelle interaction provides increased absorbance of the complex at 500 nm and higher fluorescence enhancement, allowing the detection of 0.11 μg l^?1 aluminium.     

MRI findings in osteofibrous dysplasia

A case of osteofibrodysplasia of the long bones in a 4-year-old girl is reported with ipsilateral tibial and fibular involvement. The radiological pattern of the lesions suggested fibrodysplasia but not their MRI signal characteristics. This diagnostic imaging mismatch and the bifocality of the lesion were the tell-tale indications for the confirmatory bone biopsy yielding osteofibrous dysplasia of Campanacci.     

Determination of trace amounts of cobalt in water by solid-phase spectrophotometry after preconcentration on a nitroso R salt chelating resin

A sensitive method for the determination of microamounts of cobalt by ion-exchanger spectrophotometry has been developed. The chromogenic agent, Nitroso-R-Salt (NRS), was loaded on an anionic-exchange resin (Amberlite CG-400). The absorbance of the NRS-cobalt complex on the chelating resin was measured at 508 nm. The best conditions for the preconcentration of cobalt on the resin before the spectrophotometric determination were a pH value of 6, temperature of 80 °C, and heating times of 45 or 90 min for 50 and 400 ml of sample, respectively. The detection limits were 27 ng/ml (50-ml samples) and 1.8 ng/ml (400-ml samples). Interference by other metals was investigated. The method is useful for determination of cobalt in natural waters.     

Detection efficiency calculations using Geant4 for a broad-energy germanium gamma spectrometer

In assistance of radionuclide measurements at Canada’s Comprehensive Nuclear-Test-Ban Treaty (CTBT) laboratory, a Geant4 Monte Carlo application has been developed in simulating a broad-energy germanium detector and calculating detection efficiencies. The detector model was optimized in a reliable and non-biased manner through simultaneous tuning on gap distance and detector dimension, and was validated over various realistic measurement scenarios. All work is based on a series of experiments which covers the typical energy range of gamma radiation in environmental analysis, and considers the variety of the CTBT sample type, dimension and distance-to-detector. In all cases, the predicted efficiencies are consistent with the empirical ones within 5%, with a typical deviation of 3% in majority.     

Picture change error correction of radon atom electron density

The importance of the picture change error (PCE) correction in the quasirelativistic electron density of radon atom is presented. PCE correction is considered for the infinite order two-component (IOTC) and second order Douglas-Kroll-Hess (DKH2) wave functions. Implementation details of PCE correction of electron density are outlined. The result section presents the radial distributions of electron density ρ(r) and the 4πr(2)ρ(r) function of the radon atom in the nuclear region. The PCE corrected and contaminated DKH2, IOTC electron densities are presented and compared with the Dirac-Coulomb Hamiltonian and nonrelativistic electron densities. Besides, some additional effects in electron density and SCF energy are considered, such as spin-orbit coupling, the inclusion of the Gaunt term, and the finite nucleus model effects. The effects of p(2)Vp(2) and p(2)ρ(r)p(2) analytic integral classes within IOTC Hamiltonian and PCE correction of IOTC electron density are considered.     

Infrared microspectroscopic study of the thermo-oxidative degradation of hydroxy-terminated polybutadiene/isophorone diisocyanate polyurethane rubber

Hydroxy-terminated polybutadiene/isophorone diisocyanate (HTPB/IPDI) polyurethane rubber which was aged in air at elevated temperatures has been studied by infrared microspectroscopy. Spectra were collected in transmission mode on microtomed samples. Analysis of sets of spectra taken across the sectioned material showed that most of the degradation occurred in the polybutadiene part of the polymer and that the urethane linkage was essentially unchanged. The trans isomer of the polybutadiene appears to be preferentially degraded compared with the vinyl isomer. The IR technique does not provide significant information about the cis isomer. The IR spectra indicated that likely degradation products included acids, esters, alcohols, and small amounts of other products containing a carbonyl functional group. Band area ratios, supported by a principal components analysis, were used to derive degradation profiles for the material. These profiles were steep-sided indicating an oxygen diffusion limited process.