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131.
Patrycja Wytrych Jzef Utko Julia Kak Maciej Ptak Mariusz Stefanski Tadeusz Lis Jolanta Ejfler ukasz John 《Molecules (Basel, Switzerland)》2022,27(1)
In alkali metal and lanthanide coordination chemistry, triphenylsiloxides seem to be unduly underappreciated ligands. This is as surprising as that such substituents play a crucial role, among others, in stabilizing rare oxidation states of lanthanide ions, taking a part of intramolecular and molecular interactions stabilizing metal-oxygen cores and many others. This paper reports the synthesis and characterization of new lithium [Li4(OSiPh3)4(THF)2] (1), and sodium [Na4(OSiPh3)4] (2) species, which were later used in obtaining novel gadolinium [Gd(OSiPh3)3(THF)3]·THF (3), and erbium [Er(OSiPh3)3(THF)3]·THF (4) configuration, it can result in res were determined for all 1–4 compounds, and in addition, IR, Raman, absorption spectroscopy studies were conducted for 3 and 4 lanthanide compounds. Furthermore, direct current (dc) variable-temperature magnetic susceptibility measurements on polycrystalline samples of 3 and 4 were carried out in the temperature range 1.8–300 K. The 3 shows behavior characteristics for the paramagnetism of the Gd3+ ion. In contrast, the magnetic properties of 4 are dominated by the crystal field effect on the Er3+ ion, masking the magnetic interaction between magnetic centers of neighboring molecules. 相似文献
132.
A notion of anin-tree is introduced. It is then used to characterize and count plane embeddings of outerplanar graphs. In-trees have also been applied in the study of independent vertex covers of faces in outerplanar graphs.This research was partially supported by the grant RP.I.09, from the Institute of Informatics, University of Warsaw. Hospitality of the Institute of Datalogy, University of Copenhagen where this research has been completed is gratefully acknowledged. 相似文献
133.
Turowski M Yamakawa N Meller J Kimata K Ikegami T Hosoya K Tanaka N Thornton ER 《Journal of the American Chemical Society》2003,125(45):13836-13849
Hydrogen/deuterium isotope effects on hydrophobic binding were examined by means of reversed-phase chromatographic separation of protiated and deuterated isotopologue pairs for a set of 10 nonpolar and low-polarity compounds with 10 stationary phases having alkyl and aryl groups bonded to the silica surface. It was found that protiated compounds bind to nonpolar moieties attached to silica more strongly than deuterated ones, demonstrating that the CH/CD bonds of the solutes are weakened or have less restricted motions when bound in the stationary phase compared with the aqueous solvent (mobile phase). The interactions responsible for binding have been further characterized by studies of the effects of changes in mobile phase composition, temperature dependence of binding, and QSRR (quantitative structure-chromatographic retention relationship) analysis, demonstrating the importance of enthalpic effects in binding and differentiation between the isotopologues. To explain our results showing the active role of the hydrophobic (stationary) phase we propose a plausible model that includes specific contributions from aromatic edge-to-face attractive interactions and attractive interactions of aliphatic groups with the pi clouds of aromatic groups present as the solute or in the stationary phase. 相似文献
134.
Jana Beinhauer Liangqiao Bian Hui Fan Marek Šebela Maciej Kukula Jose A. Barrera Kevin A. Schug 《Analytica chimica acta》2015
Estrone (E1), estradiols (α/β-E2), and estriol (E3) are four major metabolically active estrogens exerting strong biological activities at very low circulating concentrations. This paper reports a sensitive and efficient method with automated, on-line clean-up and detection to determine trace estrogens in a small volume of serum samples using liquid chromatography–electrospray ionization–tandem mass spectrometry directly, without off-line liquid–liquid or solid-phase extraction pretreatments. Serum aliquots (charcoal stripped fetal bovine serum, 100 μL) were spiked with four estrogen standards and their corresponding isotope-labeled internal standards, then bulk derivatized with 2-fluoro-1-methyl-pyridium p-toluenesulfonate (2-FMP) to establish the calibration curves and perform method validation. Calibration was established in the concentration ranges of 5–1000 pg mL−1, and demonstrated good linearity of R2 from 0.9944 to 0.9997 for the four derivatized estrogens. The lower detection limits obtained were 3–7 pg mL−1. Good accuracy and precision in the range of 86–112% and 2.3–11.9%, respectively, were observed for the quality control (QC) samples at low, medium, and high concentration levels. The stability tests showed that the derivatized serum samples were stable 8 h after derivatization at room temperature and at least to 48 h if stored at −20 °C. The method was applied to measure trace estrogens in real human and bovine serum samples, and three of four estrogen compounds studied were observed and quantified. 相似文献
135.
The synthesis of 2-phenylsparteine-N16-oxide (7) and its perchlorate salt (7-H+) was carried out. On the basis of spectral data, and by comparison with appropriate sparteine-N-oxides, the mechanism of formation and the structures of the two new compounds were proposed. It was found, the basicity of the new N-oxide is unexpectedly high and comparable to the basicity of quaternary ammonium hydroxides. The structure and the strength of intramolecular H-bond in 7-H+ makes 7 an excellent “catcher” proton or specific ”sponge” proton. 相似文献
136.
Dramatic rate acceleration was observed for N-sulfopropylation of heterocyclic compounds (1a-h) using 1,3-propane sultone(2) under microwave irradiation affording the N-sulfopropylated compounds (3a-h) in 68–95% yield. 相似文献
137.
138.
Zbigniew Florjaczyk Wodzimierz Krawiec Wadysaw Wieczorek Maciej Siekierski 《Journal of Polymer Science.Polymer Physics》1995,33(4):629-635
The conducting properties of solid electrolytes comprising random poly(ethylene oxide-co-propylene oxide) (of 84 : 16 monomer units mole ratio) and lithium, sodium, potassium, cesium, and rubidium salts have been studied. The systems containing some lithium or sodium salts achieved conductivity levels as high as 10?5–10?4 S/cm at ambient temperature and greater than 10?3 S/cm at 100°C. However, the systems with rubidium and cesium salts exhibit conductivities a few orders of magnitude smaller. DSC studies show that the electrolytes studied are characterized by a high content of an amorphous phase (95–100%). It is suggested that the copolymer exhibits lower complexing abilities than that of poly(ethylene oxide), which results in a higher flexibility of electrolytes containing small cations and poor dissociation of the salts having large cations. © 1995 John Wiley & Sons, Inc. 相似文献
139.
We introduce a Hamiltonian system with many degrees of freedom for which the nonvanishing of (some) Lyapunov exponents almost everywhere can be established analytically.Supported in part by the Sloan Foundation and the NSF Grant DMS-8807077 相似文献
140.
Maciej Walcerz Ewa Bulska Adam Hulanicki 《Fresenius' Journal of Analytical Chemistry》1993,346(6-9):622-626
Summary A detailed study of interfering processes in the determination of As, Sb and Se using a twin-channel hydride generation flow-system is presented. The influence of As, Sb, Se and Sn on all three studied elements has a similar character and occurs in the gas phase only. In the presence of bismuth and tellurium interferences occur also in the liquid phase. It was found that arsenic and antimony may influence the analytical signals of elements with analytical lines in the range from 190 to 235 nm by non-specific absorption due to molecular band spectra.Dedicated to Professor Dr. Wilhelm Fresenius on the occasion of his 80th birthday 相似文献