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At least 1,063 records · Page 59Linked to original sources
PubMed2004

Phase stability in the systems AeAl(2-x)Mgx (Ae = Ca, Sr, Ba): electron concentration and size controlled variations on the laves phase structural theme.

The systems AeAl(2-x)Mgx (Ae = Ca, Sr, Ba) display electron concentration induced Laves phase structural changes. However, the complete sequence MgCu2 --> MgNi2 --> MgZn2 with increasing x (decreasing electron count) is only observed for Ae = Ca. Compounds SrAl(2-x)Mgx (0 < x < or = 2) and BaAl(2-x)Mgx (x = 0.85 and 2.0) were synthesized and structurally characterized by X-ray diffraction experiments. For the Sr system the structural sequence CeCu2 --> MgNi2 --> MgZn2 occurs with increasing Mg content x. Thus, larger Sr does not allow the realization of the MgCu2 structure at low x. For Ae = Ba a binary compound BaAl2 does not exist, but more Ba-rich Ba7Al13 forms. The reinvestigation of the crystal structure of Ba7Al13 by selected area and convergent beam electron diffraction in a transmission electron microscope revealed a superstructure, which subsequently could be refined from single X-ray diffraction data. The formula unit of the superstructure is Ba21Al40 (space group P31m, Z = 1, a = 10.568(1) angstroms, c = 17.205(6) angstroms). In Ba21Al40 a size match problem between Ba and Al present in Ba7Al13 is resolved. The structure of Ba7Al13 (Ba21Al40) can be considered as a Ba excess variant of the hexagonal MgNi2 Laves phase type structure. An incommensurately modulated variant of the MgNi2 structure is obtained for phases BaAl(2-x)Mgx with x = 0.8-1. At even higher Mg concentrations a structural change to the proper MgZn2 type structure takes place.

Journal Article↗
PubMed2004

Gas-phase and solution-phase polymerization of epoxides by Cr(salen) complexes: evidence for a dinuclear cationic mechanism.

The gas-phase reactions of a series of mass-selected mononuclear and dinuclear Cr(salen) complexes with propylene oxide suggest that the enhanced reactivity of the dinuclear complexes in gas-phase and in solution may derive from a dicationic mechanism in which the alkoxide chain is mu(2)-coordinated to two Lewis acidic metal centers. The double coordination is proposed to suppress backbiting, and hence chain-transfer in the gas-phase homopolymerization of epoxides.

Journal Article↗
PubMed2001

Comparisons in the behavior of stable copper(II), silver(II), and gold(II) complexes in the gas phase: are there implications for condensed-phase chemistry?

Experiments conducted in the gas phase have led to the formation of a series of stable gold(II) complexes with nitrogen- and oxygen-containing ligands. Such complexes are very rare in condensed-phase chemistry. However, there is also a significant group of potential ligands, for example, H2O and NH3, for which stable complexes could not be formed. There are strong similarities between these observations and earlier results presented for silver(II), but both metal ions behave markedly different from copper(II). As a group the majority of successful gold(II) ligands are characterized by being good sigma donor-pi acceptor molecules; however, it is also possible to understand the ability of individual ligands to stabilize the metal ion in terms of a simple electrostatic model. Application of the latter reveals a semiquantitative trend between the physical properties of a ligand, e.g. ionization energy, dipole moment, and polarizability, and the ligand's ability to stabilize either Cu(II), Ag(II), or Au(II). The model successfully accounts for the preference of Cu(II) for aqueous chemistry, in comparison to the complete absence of such behavior on the part of Ag(II) and Au(II). Ligands from recent examples of stable condensed-phase gold(II) complexes appear to meet at least one of the criteria identified from the model.

Journal Article↗
PubMed2002

NMR imaging of the distribution of the liquid phase in a catalyst pellet during alpha-methylstyrene evaporation accompanied by its vapor-phase hydrogenation.

This communication reports the first application of NMR imaging to study the progress of a multiphase heterogeneous catalytic reaction in situ. Various stationary regimes of alpha-methylstyrene (AMS) hydrogenation on a single Pt/gamma-Al2O3 catalyst pellet have been investigated. The two-dimensional maps of the liquid-phase distribution within the pellet have been obtained in the course of the catalytic reaction, with the pellet temperature rising up to 185 degrees C. The large liquid-phase concentration gradients have been shown to exist under conditions of liquid AMS evaporation accompanied by its vapor-phase hydrogenation. It has been demonstrated that despite a substantial broadening of the NMR lines of liquids permeating porous solids the quantification of the relative amounts of AMS and the major reaction product cumene with spatial resolution across the pellet is feasible.

Journal Article↗
PubMed2003

The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism.

The mechanism of the ozonation of isopropyl alcohol was investigated for the gas and the solution phase using second-order many body perturbation theory and density functional theory (DFT) with the hybrid functional B3LYP and a 6-311++G(3df,3pd) basis set. A careful analysis of calculated energies (considering thermochemical corrections, solvation energies, BSSE corrections, the self-interaction error of DFT, etc.) reveals that the gas-phase mechanism of the reaction is dominated by radical or biradical intermediates while the solution-phase mechanism is characterized by hydride transfer and the formation of an intermediate ion pair that includes the HOOO(-) anion. The product distribution observed for the ozonation in acetone solution can be explained on the basis of the properties of the HOOO(-) anion. General conclusions for the ozonation of alcohols and the toxicity of ozone (inhaled or administered into the blood) can be drawn.

Journal Article↗
PubMed1998

Reversed-Phase Ion-Pair High-Performance Liquid Chromatographic Quantitation of Difethialone Residues in Whole-Body Rodents with Solid-Phase Extraction Cleanup.

A reversed-phase ion-pair high-performance liquid chromatographic method was developed for the determination of difethialone residues in laboratory rats (Rattus norvegicus). Difethialone was extracted from rat tissue with chloroform/acetone/formic acid. The extracts were cleaned up by a solid-phase extraction (SPE) procedure using both silica and aminopropyl SPE sorbents, concentrated, and analyzed by reversed-phase ion-pair high-performance liquid chromatography. Difethialone was quantitated via ultraviolet absorbance at 262 nm. A surrogate compound, brodifacoum, was used to correct for method performance. The mean surrogate-corrected recoveries for whole ground rodent fortified at 0.2, 1.0, and 20 µg/g difethialone were 92.3 +/- 7.7, 84.8 +/- 6.6, and 90.2 +/- 3.1%, respectively. The method limit of detection was 0.054 µg/g.

Journal Article↗
PubMed1996

Gas-Phase and Solution-Phase Homolytic Bond Dissociation Energies of H-N(+) Bonds in the Conjugate Acids of Nitrogen Bases.

The oxidation potentials of 19 nitrogen bases (abbreviated as B: six primary amines, five secondary amines, two tertiary amines, three anilines, pyridine, quinuclidine, and 1,4-diazabicyclo[2,2,2]octane), i.e., E(ox)(B) values in dimethyl sulfoxide (DMSO) and/or acetonitrile (AN), have been measured. Combination of these E(ox)(B) values with the acidity values of the corresponding acids (pK(HB)(+)) in DMSO and/or AN using the equation: BDE(HB)(+) = 1.37pK(HB)(+) + 23.1 E(ox)(B) + C (C equals 59.5 kcal/mol in AN and 73.3 kcal/mol in DMSO) gave estimates of solution phase homolytic bond dissociation energies of H-B(+) bonds. Gas-phase BDE values of H-B(+) bonds were estimated from updated proton affinities (PA) and adiabatic ionization potentials (aIP) using the equation, BDE(HB(+))(g) = PA + aIP - 314 kcal/mol. The BDE(HB)(+) values estimated in AN were found to be 5-11 kcal/mol higher than the corresponding gas phase BDE(HB(+))(g) values. These bond-strengthening effects in solution are interpreted as being due to the greater solvation energy of the HB(+) cation than that of the B(+*) radical cation.

Journal Article↗
PubMed2005

Theory of retention in reversed phase liquid chromatography with ternary mobile phases.

The partition model of retention is developed for reversed phase liquid chromatography with multicomponent mobile phases. Simple equations for the retention and selectivity in ternary mobile phases are derived. For the systems in which the ratio of volume fractions of organic modifiers remains fixed, new linear dependences for retention factor and selectivity are proposed. These equations are successfully used to describe experimental data found in the literature. An influence of the nature of organic solvents and proportion in which they are mixed on retention and selectivity is discussed.

Journal Article↗
PubMed2006

Cluster phase chemistry: gas-phase reactions of anionic sodium salts of dicarboxylic acid clusters with water molecules.

A homologous series of anionic gas-phase clusters of dicarboxylic acids (oxalic acid, malonic acid, succinic acid, glutaric acid, and adipic acid) generated via electrospray ionization (ESI) are investigated using collision-induced dissociation (CID). Sodiated clusters with the composition (Na(+))(2)(n+1)(dicarboxylate(2-)(n+1) for singly charged anionic clusters, where n = 1-4, are observed as major gas-phase species. Isolation of the clusters followed by CID results mainly in sequential loss of disodium dicarboxylate moieties for the clusters of succinic acid, glutaric acid, and adipic acid (C4-C6). However, all oxalate (C2) and malonate (C3) clusters and dimers (n = 1) of succinate (C4) and glutarate (C5) exhibit more complex chemistry initiated by collision of the activated cluster with water molecules. For example, with water addition, malonate clusters dissociate to yield sodium acetate, carbon dioxide, and sodium hydroxide. More generally, water molecules serve as proton donors for reacting dicarboxylate anions in the cluster and introduce energetically favorable dissociation pathways not otherwise available. Density functional theory (DFT) calculations of the binding energy of the cluster correlate well with the cluster phase reactions of oxalate and malonate clusters. Clusters of larger dicarboxylate ions (C4-C6) are more weakly bound, facilitating the sequential loss of disodium dicarboxylate moieties. The more strongly bound small dicarboxylate anions (oxalate and malonate) preferentially react with water molecules rather than dissociate to lose disodium dicarboxylate monomers when collisionally activated. Implications of these results for the atmospheric aerosol chemistry of dicarboxylic acids are discussed.

Anions↗
PubMed2000

Effects of phototherapy on the phase relationship between sleep and body temperature rhythm in a delayed sleep phase syndrome case.

We examined polysomnography (PSG) and body temperature of a patient with delayed sleep phase syndrome (DSPS) who was successfully treated with only phototherapy. This case showed a possible improvement of the phase relationship between sleep and body temperature rhythm given that the time of minimum body temperature (mBT) shifted to the latter portion of the sleep phase after constant phototherapy.

Adult↗
PubMed2001

Dual phase helical CT versus portal venous phase CT for the detection of colorectal liver metastases: correlation with intra-operative sonography, surgical and pathological findings.

AIM: To assess whether dual phase helical computed tomography (DPCT) of the liver improves the detection of colorectal liver metastases compared with portal venous phase (PVP) imaging alone. MATERIALS AND METHODS: DPCT was performed in 33 consecutive patients before laparotomy for resection of colorectal liver metastases. CT comprised 8-mm slice collimation with a pitch of 1 to 1.25; imaging was commenced 20-25 and 65-70 s after the start of injection of 150 ml of contrast medium at 5 ml/s to coincide with hepatic arterial phase (HAP) and PVP contrast enhancement, respectively. Four blinded observers independently reviewed the HAP, PVP and DPCT images recording the site and size of all lesions. Alternative-free response receiver operating characteristic (AFROC) methodology was used to analyse the results, which were correlated with surgery, intra-operative ultrasound and histology. RESULTS: The mean observer sensitivities for malignant lesion detection were 75.3% for DPCT, 69.7% for PVP imaging and 66.7% for HAP imaging alone. There was a statistically significant improvement in malignant lesion detection using DPCT when compared with PVP imaging alone (P < 0.05). The mean areas under the AFROC curves were 0.84 for DPCT and 0.82 for PVP (P < 0.03) imaging alone. CONCLUSION: The detection of colorectal liver metastases was marginally better with DPCT than with PVP imaging alone, but the discovery of additional lesions did not affect the management of any of the patients in this study.

Aged↗
PubMedDate not supplied

[Continuity and the quality of medical care for the cardiac patient: cardiac rehabilitation and its interfaces to acute care (phase I) and the process of coming back (phase III)].

Cardiac rehabilitation plays a pivotal role in the care for cardiac patients. Yet without sufficient continuity in the care process, the good results achieved in the different stages of therapy and recovery may not last. The aim of this contribution is to highlight the interfaces of cardiac rehabilitation in regard of process continuity as an aspect of the quality of health care. The results show that continuity between the acute care unit and inpatient rehabilitation programmes (phase I - phase II) seems to be sufficient whereas integrating phases II and III may be open for optimizing.

Aftercare↗
PubMed1998

[Flow quantification of intracardiac shunt volumes using MR phase contrast technique in the breath holding phase].

PURPOSE: Comparison of a breath-hold, velocity-encoded, phase-difference magnetic resonance (MR) sequence for intracardiac shunt flow measurement with the invasive shunt size determination by oximetry. PATIENTS AND METHODS: 10 patients with different cardiac shunts (6 ASD/3 VSD/1 PDA) and four healthy individuals were investigated using a 1.5 Tesla Siemens Vision system. For flow measurements a breath-hold, velocity-encoded, phase-difference magnetic resonance (MR) sequence was used ('through plane', FLASH 2D-sequence, TR/TE 110/5 ms, 'velocity encoding' 250 cm/s). Mean flow (ml/R-R interval) in the ascending aorta, the pulmonary trunk, and the right and left pulmonary arteries was determined. The ratio of the mean flow in the pulmonary circulation (Qp: sum of the mean flows in the right and left pulmonary arteries) and the systemic circulation (Qs: mean flow in the proximal aorta) was compared with the Qp/Qs ratios determined by the invasive oxymetric technique. Oximetry was performed within 24 hours after MR imaging. RESULTS: In the 4 healthy individuals MR flow measurement yielded a Qp/Qs ratio of 0.96 +/- 0.15. In the 10 patients with the various shunt defects, the non-invasive shunt determination by MR gave a Qp/Qs ratio of 2.09 +/- 0.67. The percentage of the calculated shunt sizes was 47.05 +/- 17.45%. In the comparison with the results determined by the invasive oxymetric technique, the MR data showed a strong correlation of r = 0.87. CONCLUSIONS: Breath-hold, velocity-encoded, phase-difference MR-technique enables a reliable quantification of cardiac shunts within a short acquisition time.

Adult↗
PubMed2006

n-pentanol at high pressures: rotational isomerism in the liquid phase and the liquid-solid phase transition.

The vibrational spectrum of liquids constituted of chain molecules is difficult to analyze because it may have contributions of different rotational isomers. In turn, with a proper vibrational assignment, this feature allows us to extract information about the effect of temperature or pressure on the molecular conformations in the liquid state. In this regard, the information on the vibrational spectrum in the solid phase greatly simplifies the vibrational analysis of the different rotational conformers existing in the liquid, as the molecules usually present all-trans conformations in the crystalline state. Here we report room-temperature Raman experiments on n-pentanol performed in a sapphire-anvil cell up to 3 GPa. A detailed analysis of the liquid-solid phase transition occurring at 1.3 GPa is provided. The analysis of the Raman spectrum in the solid phase allows the identification of the bands due to the different rotational isomers present in the liquid. The analysis of the spectral region corresponding to skeletal vibrations of the carbon chain (800-1200 cm(-1)) indicates that gauche conformers are promoted by the application of pressure. The analysis of the intensity ratio of those bands assigned to trans and gauge conformations is used to calculate the change in molecular volume ascribed to the trans-gauge isomerization process. We find a value similar to that found in n-alkanes, i.e., -0.88 cm(3) mol(-1). In addition, we find indication that pressure varies the proportions of the different gauge conformers. Thus, it appears that the GTTt to TGTt transition in the carbon chain is favored at high pressures. As expected, a smaller change in the molecular volume accompanies this conformation change.

Journal Article↗
PubMed1990

Phospholipid in the hexagonal II phase is immunogenic: evidence for immunorecognition of nonbilayer lipid phases in vivo.

Immunization of mice with phosphatidylethanolamine in the hexagonal II phase but not the bilayer phase resulted in the induction of anti-phospholipid antibodies. These antibodies, which were strongly reactive with phosphatidylethanolamine and crossreactive with cardiolipin, had functional lupus anticoagulant activity and were characteristic of autoantibodies common in patients with autoimmune disease. Recognition of the hexagonal II phase by the afferent limb of the immune system suggests that nonbilayer phospholipids can arise in the course of membrane remodeling and induce the autoantibodies of disease.

Animals↗
PubMed2002

Reference phase-shifter for measuring high power microwave impedance by using a phase modulation method.

A basic mechanical phase-shifter is described and proposed for use as a reference circuit for impedance measurements with a phase modulation method. It consists of a section of a curved rectangular waveguide, the length of which is mechanically varied with a stepper motor. The phase-shifter functions without gears. It can be used successfully in industrial set-ups with a pulsed or CW generator which are of low stability in frequency and in amplitude.

Journal Article↗
PubMed2003

Influence of mobile phase composition on retention factors in different HPLC systems with chemically bonded stationary phases.

The influence of mobile phase composition on the retention of selected test analytes in different normal- and reversed-phase chromatographic systems is studied. A novel adsorption model for an accurate prediction of the analyte retention in the column chromatography with binary mobile phase is proposed. Performance of the model is compared with the retention model reported in the literature. Both models are verified for different HPLC systems by use of three criteria: (a). the sum of squared differences between the experimental and theoretical data, (b). approximation of the standard deviation, and (c). the Fisher test.

Journal Article↗
PubMed2005

Adsorption-driven retention in normal-phase chromatography with ternary mobile phases.

The model for retention in chromatographic systems using ternary mobile phases is considered. The driving force for the separation is assumed to be only a difference in adsorptive properties of a solute and all solvents. The effects of mobile phase composition are discussed. A series of very simple dependences between parameters characterizing retention in ternary and binary solvents is presented. The linear relationship is proposed to predict the capacity factor in the ternary mobile phase, for which the ratio of mole fractions of two less-polar solvents remains fixed. Theoretical concepts are verified by comparing the calculated values with experimental data measured in the entire concentration region.

Journal Article↗