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11.
The method is based on the separation of Tl(I) as Tl(2)HPMo(12)O(40), stripping of the molybdate, and measurement of the peak current in differential-pulse polarography of the molybdenum. The calibration graph is linear over the range 2-12 ppm of thallium. The relative standard deviation is 1.2% (7 replicates each containing 500 microg of thallium). The current due to reduction of the molybdenum is three times that for reduction of the equivalent amount of Tl(I) in the thallous phosphomolybdate precipitate, making the indirect approach more sensitive than direct polarographic determination of the Tl(I). 相似文献
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Michael Cargnelli M. Bazzi G. Beer C. Berucci L. Bombelli A. M. Bragadireanu A. Clozza G. Corradi C. Curceanu A. d’Uffizi C. Fiorini F. Ghio B. Girolami C. Guaraldo R. S. Hayano M. Iliescu T. Ishiwatari M. Iwasaki P. Kienle P. Levi Sandri V. Lucherini J. Marton S. Okada D. Pietreanu K. Piscicchia M. Poli Lener T. Ponta R. Quaglia A. Rizzo A. Romero Vidal E. Sbardella A. Scordo H. Shi D. L. Sirghi F. Sirghi H. Tatsuno A. Tudorache V. Tudorache O. Vazquez Doce E. Widmann J. Zmeskal 《Hyperfine Interactions》2012,209(1-3):121-126
The $\overline{K}N$ system at rest plays a key role for the understanding of strong interaction of hadrons with strangeness involved. The experiment SIDDHARTA used X-ray spectroscopy of kaonic atoms to measure the strong interaction induced shift and width of the ground state. It was the first experiment on kaonic He3 and deuterium ever, kaonic hydrogen was measured with improved precision resulting in $\epsilon_{1s} = -283 \pm 36 \mbox{(stat)} \pm 6 \mbox{(syst)}$ eV and $\Gamma_{1s} = 541 \pm 89 \mbox{(stat)} \pm 22 \mbox{(syst)}$ eV. Additionally a scheme for an improved future experiment on kaonic deuterium is introduced in this contribution. 相似文献
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Adel Mostafa Hassan S. Bazzi 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,74(1):180-187
The interactions of the electron donors 2-aminopyridine (2APY) and 3-aminopyridine (3APY) with the π-acceptors tetracyanoethylene (TCNE), 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ), 2-chloro-1,3,5-trinitrobenzene (picryl chloride, PC), and 2,3,5,6-tetrachloro-1,4-benzoquinone (chloranil) were studied spectrophotometrically in chloroform at room temperature. The electronic and infrared spectra of the formed molecular charge transfer (CT) complexes were recorded. Photometric titration showed that the stoichiometries of the reactions were fixed and depended on the nature of both the donor and the acceptor. The molecular structures of the CT-complexes were, however, independent of the position of the amino group on the pyridine ring and were formulated as [(APY)(TCNE)], [(APY)(DDQ)], [(APY)(PC)], and [(APY) (chloranil)]. The formation constants (KCT), charge transfer energy (ECT) and molar extinction coefficients (CT) of the formed CT-complexes were obtained. 相似文献
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The synthesis, X-ray structure, and electrochemical and photophysical characterization of [Ru(phen)(2)dpq-n][PF(6)](2) (phen = phenanthroline, dpq-n = dipyridoquinoxaline-norbornene) are described. This complex contains a Ru(phen)(3)(2+) moiety in close conjugation with a norbornene unit and is the first example of a Ru(II) diimine complex capable of undergoing ring-opening metathesis polymerization. Luminescence studies of this complex showed an increase in quantum efficiency in polar solvents and in water. Preliminary ring-opening metathesis polymerization studies, carried out at low monomer-to-initiator ratio, showed the formation of an oligomeric mixture composed mainly of the dimer of this complex. This dimer exhibits photophysical and redox properties similar to those of the monomer, indicating that the Ru(phen)(3)(2+) moiety remains intact during the polymerization. 相似文献
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Kristian Piscicchia Johann Marton Sergio Bartalucci Massimiliano Bazzi Sergio Bertolucci Mario Bragadireanu Michael Cargnelli Alberto Clozza Raffaele Del Grande Luca De Paolis Carlo Fiorini Carlo Guaraldo Mihail Iliescu Matthias Laubenstein Marco Miliucci Edoardo Milotti Fabrizio Napolitano Andreas Pichler Alessandro Scordo Hexi Shi Diana Laura Sirghi Florin Sirghi Laura Sperandio Oton Vazquez Doce Johann Zmeskal Catalina Curceanu 《Entropy (Basel, Switzerland)》2020,22(11)
The VIP collaboration is performing high sensitivity tests of the Pauli Exclusion Principle for electrons in the extremely low cosmic background environment of the underground Gran Sasso National Laboratory INFN (Italy). In particular, the VIP-2 Open Systems experiment was conceived to put strong constraints on those Pauli Exclusion Principle violation models which respect the so-called Messiah–Greenberg superselection rule. The experimental technique consists of introducing a direct current in a copper conductor, and searching for the X-rays emission coming from a forbidden atomic transition from the L shell to the K shell of copper when the K shell is already occupied by two electrons. The analysis of the first three months of collected data (in 2018) is presented. The obtained result represents the best bound on the Pauli Exclusion Principle violation probability which fulfills the Messiah–Greenberg rule. 相似文献
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K. Barouni A. Kassale L. Bazzi R. Salghi B. Hammouti A. Albourine S. El Issami O. Jbara M. Bouachrine 《Research on Chemical Intermediates》2014,40(3):991-1002
Inhibition of corrosion of copper in 1M HNO3 solution by four amino acids, proline (Pro), phenylalanine (Phe), tyrosine (Tyr), and tryptophan (Try), has been studied by use of gravimetric and electrochemical polarization measurements. The results obtained the from two different techniques are comparable, and show that Tyr and Try act as good inhibitors of corrosion of copper in 1 mol L?1 HNO3. Correlation between inhibition efficiency and quantum chemical calculations, performed using semi empirical (AM1 and MNDO) and ab-initio methods, is discussed. 相似文献
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Ring opening metathesis polymerization (ROMP) of five- to eight-membered cyclic olefins: Computational,thermodynamic, and experimental approach 下载免费PDF全文
Antsar R. Hlil Janos Balogh Salvador Moncho Haw-Lih Su Robert Tuba Edward N. Brothers Mohammed Al-Hashimi Hassan S. Bazzi 《Journal of polymer science. Part A, Polymer chemistry》2017,55(18):3137-3145
Ring opening metathesis polymerization (ROMP) of a series of low-strain cyclic olefins and their hydroxyl derivatives using second generation Hoveyda–Grubbs catalyst has been investigated. Additionally, density functional theory (DFT) calculations were performed to evaluate the ring strain energies of the cyclic olefins and their hydroxyl derivatives, coupled with kinetic studies for the ROMP reactions. It was found that among different ring size monomers, Cy8 having a relatively moderate ring strain energy in comparison with the other cyclic olefins, exhibited the highest monomer conversion. The effect of temperature (0, 10, 15, and 25 °C) and monomer concentration (1 M; 2.5 M and 5 M for Cy5 ; and 1 M and 5 M for Cy7 ) for the cyclic olefins Cy5 and Cy7 were investigated. In general, the experimental results for the kinetic ROMP studies obtained using complex HG2 correlate really well with the DFT calculations determined for the ring strain energies of the cyclic olefins. For comparison, DFT calculations predicted the following trend for the ring strain energies Cy8 > Cy5 > Cy7 > Cy6 , and the polymerizations carried out experimentally followed the same trend in terms of monomer conversion, with the exception of Cy5 and Cy7 at lower concentrations, which followed this trend Cy8 > Cy7 > Cy5 > Cy6 . © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3137–3145 相似文献
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A. Ebrahimi M. Habibi-Khorassani S. Bazzi 《Journal of the Iranian Chemical Society》2011,8(4):908-918
The effects of structural parameters and intramolecular interactions on N-glycosidic bond length in 3-methyl-2??- deoxyadenosine (3MDA) and 2??-deoxyadenosine (DA) were investigated employing quantum mechanical methods. All calculations were performed at B3LYP/6-311++G** level in the gas phase. The N-glycosidic bond length strongly depends on sugar configuration; it is shorter in syn conformation relative to anti in many cases where they have the same sugar ring configuration. The sugar conformation can influence the N-glycosidic bond through interaction with the O4?? atom. The impact of intramolecular improper hydrogen bonds and H-H bonding interactions on N-glycosidic bond length was investigated in DA and 3MDA and their modeled structures. Improper hydrogen bonds decrease N-glycosidic bond length while H-H bonding interactions increase it. 相似文献