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1.
2.
Hall AC Suarez C Hom-Choudhury A Manu AN Hall CD Kirkovits GJ Ghiriviga I 《Organic & biomolecular chemistry》2003,1(16):2973-2982
The synthesis, cation binding and transmembrane conductive properties of a novel group of synthetic ion channels containing a redox-active centre are described. Experiments using a black lipid membrane preparation revealed that these compounds function effectively as ion channels. Subsequent 23Na NMR spectroscopy studies focused on a synthesized ion channel with a ferrocene centre. When incorporated in vesicular bilayers, this channel was demonstrated to support a Na+ flux that was at least six times faster than ion transport by monensin. Since oxidation of the ferrocene moiety completely inhibited the Na+ transport, the redox-active centre provides a potential mechanism for controlling ion flux. 相似文献
3.
S. Suarez A. R. Goñi W. Meckbach P. R. Focke 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1987,6(1):55-59
Using a coaxial cylindric electron spectrometer and an electrostatic ion energy analyzer in tandem, a direct measurement of the difference of the energy of convoy peak electron and the electron equivalent ion energy of protons emerging from the downstream surface of C, Au and Al foils is performed in the proton energy range from 60 to 250 keV. This measurement is made possible using the accepted evidence that for a gas target these energies are equal. It is found that also for the beam foil convoy peak electrons, within an experimental average uncertainty of about ±0.1 eV, there is no difference between these energies. If one accepts that the origin of convoy electrons is from inside the solid, the conclusion is that no retardation by the solid surface potential barrier, which is of the order of a few eV, is observed. This is attributed to the strong electron-ion Coulomb interaction which almost completely overshadows the force exerted on the electron by the field of the surface barrier. 相似文献
4.
The catalytic system methylaluminoxane (MAO) and bis(n-butylcyclopentadienyl)zirconium dichloride ((nBuCp)2ZrCl2) was immobilized on commercial silica, silica-alumina and aluminophosphate calcined at different temperatures. The properties of the supports were determined by using N2 adsorption-desorption isotherms at 77 K, FT-IR spectroscopy and SEM. After aluminium and zirconium impregnation, the catalysts were analyzed by ICP-AES, FT-IR and UV-vis spectroscopy. Ethylene polymerizations were carried out in a Schlenk tube at 70 °C and 1.2 bar of ethylene pressure. The polyethylene obtained was characterized by GPC, DSC and SEM.Catalysts supported on silica-alumina exhibited higher polymerization activity than those supported on silica and aluminophosphate. Besides, the activity of MAO/(nBuCp)2ZrCl2 catalytic system supported on silica-alumina and aluminophosphate decreased strongly with support calcination temperature, while remained almost constant when silica was employed as support. All these experimental features suggest a role of the support acid properties and hydroxyl group population in the generation of active polymerization species. 相似文献
5.
The photometric and fluorometric characteristics of the complex formed by 1,4-dihydroxyanthraquinone with Y(III) in 20–80% water-ethanol solution are described by the study of several variables. The stoichiometry and stability constant of the complex in the solution are 1:1 and log K = 4.57, respectively. The 1,4-dihydroxyanthraquinone-Y(III) solid complex has been prepared and studied by infrared spectroscopy and thermal analysis. The thermal behavior of this compound has been studied using thermogravimetry and differential scanning calorimetry techniques and the residue verified by X-ray diffraction. 相似文献
6.
Abstract Solid solutions Ca1-xGdxF2+x for 3 × 10?7≤ x ≤10?1 have been studied by electron paramagnetic resonance (EPR) and ionic thermal currents (ITC). The EPR experiments show the presence of two single-ion sites a cubic and a tetragonal Gd3+ center which co-exist with comparable abundances for intermediate impurity concentrations. The cubic center predominates at very low and high concentrations. Seven different relaxation processes have been identified from the ITC spectra and the variation of their intensity vs. x was measured. The absolute concentrations of the cubic and nn Gd3+ dipoles were calculated. The scavenging of interstitial fluorines by the neutral clusters explains both the abundance of cubic sites at high concentration and the variety of orientable clusters detected by ITC. 相似文献
7.
FRANCK-CONDON FACTORS AND R-CENTROIDS FOR THE GREEN-YELLOW SYSTEM OF LA16O AND LA18O ARE REPORTED. CALCULATION INCLUDES ROTATION-VIBRATION INTERACTION, AND A SIGNIFICANT VARIATION WHEN THE ROTATIONAL QUANTUM NUMBER CHANGES HAS BEEN FOUND. 相似文献
8.
Jeffrey Trautmann Alirica I. Suarez Pakamas Tongcharoensirikul Gregory W. Muth Charles M. Thompson 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):471-477
Dimethyl thiophosphite reacts with aliphatic aldehydes and ketones, Michael acceptors, and N-benzyl imines to afford excellent yields of f -hydroxy phosphonothionates, g -substituted phosphonothionates and f -amino phosphonothionates, respectively. Dealkylation of f -amino phosphonothionates affords N-benzyl f -amino phosphonothioic acids. Dimethyl thiophosphite reacts with electrophiles at a significantly greater rate than dimethyl phosphite. 相似文献
9.
10.
Carlos B. Suarez 《光谱学快报》2013,46(7):705-712
We have obtained a new set of vibrational constants of WO using available rotational and isotopic shifts measurements. Some difficulties in the analysis are pointed out. 相似文献