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141.
Vladimir A. Andreev Margarita A. Man’ko Vladimir I. Man’ko Nguyen Cong Thanh Nguyen Hung Son Stanislav D. Zakharov 《Journal of Russian Laser Research》2009,30(6):591-598
Tomographic probability representation is introduced for fermion fields. The states of the fermions are mapped onto the probability
distribution of discrete random variables (spin projections). The operators acting on the fermion states are described by
fermionic tomographic symbols. The product of the operators acting on the fermion states is mapped onto the star-product of
the fermionic symbols. The kernel of the star-product is obtained. The antisymmetry of the fermion states is formulated as
a specific symmetry property of the tomographic joint probability distribution associated with the states. 相似文献
142.
Amauri J. Paula Rodrigo Parra Maria A. Zaghete Jos A. Varela 《Solid State Communications》2009,149(39-40):1587-1590
Because of the environmental concerns, the manufacture of ceramics based on lead titanate zirconate [Pb(Zr1−xTix)O3−PZT] has been condemned because of the lead toxicity. In this context, the electromechanical properties of sodium, potassium and lithium niobate [(Na0.5−x/2K0.5−x/2Lix)NbO3−NKLN] at the morphotropic phase boundary granted these materials the position of most suitable candidate to replace PZT. However, the production of these ceramics is rather critical mainly because of a natural tendency of forming secondary phases. To help with the studies of the synthesis of this lead-free piezoceramic, this work presents an evaluation of the crystallization of the (Na0.47K0.47Li0.06)NbO3 phase by solid-state reactions. TG-DTA, XRD, dilatometric and ferroelectric hysteresis analyses indicated that a secondary phase (K3Li2Nb5O15) crystallizes at temperatures above 850 C and also during the sintering of the powders compacts at 1080 C. To prevent the formation of this phase, the addition of Na2Nb2O6.nH2O microfibers obtained through a microwave hydrothermal synthesis was performed in the sintering process. After to this addition, the suppression of the K3Li2Nb5O15 phase occurred and an increase of the NKLN electrical properties was then obtained. 相似文献
143.
Patricia Lara Margarita Paneque Prof. Dr. Manuel L. Poveda Prof. Dr. Laura L. Santos Dr. José E. V. Valpuesta Verónica Salazar Dr. Ernesto Carmona Prof. Dr. Salvador Moncho Gregori Ujaque Dr. Agustí Lledós Prof. Dr. Celia Maya Dr. Kurt Mereiter Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(36):9046-9057
Experimental and theoretical studies on equilibria between iridium hydride alkylidene structures, [(TpMe2)Ir(H){?C(CH2R)ArO }] (TpMe2=hydrotris(3,5‐dimethylpyrazolyl)borate; R=H, Me; Ar=substituted C6H4 group), and their corresponding hydride olefin isomers, [(TpMe2)Ir(H){R(H)C? C(H)OAr}], have been carried out. Compounds of these types are obtained either by reaction of the unsaturated fragment [(TpMe2)Ir(C6H5)2] with o‐C6H4(OH)CH2R, or with the substituted anisoles 2,6‐Me2C6H3OMe, 2,4,6‐Me3C6H2OMe, and 4‐Br‐2,6‐Me2C6H2OMe. The reactions with the substituted anisoles require not only multiple C? H bond activation but also cleavage of the Me? OAr bond and the reversible formation of a C? C bond (as revealed by 13C labeling studies). Equilibria between the two tautomeric structures of these complexes were achieved by prolonged heating at temperatures between 100 and 140 °C, with interconversion of isomeric complexes requiring inversion of the metal configuration, as well as the expected migratory insertion and hydrogen‐elimination reactions. This proposal is supported by a detailed computational exploration of the mechanism at the quantum mechanics (QM) level in the real system. For all compounds investigated, the equilibria favor the alkylidene structure over the olefinic isomer by a factor of between approximately 1 and 25. Calculations demonstrate that the main reason for this preference is the strong Ir–carbene interactions in the carbene isomers, rather than steric destabilization of the olefinic tautomers. 相似文献
144.
A laser-induced fluorescence (LIF) system was optimized using a solution of Micrococcus luteus in ethanol/water 50% (v/v) to obtain spectra in the gas phase of 46 bioaerosols. Experimental designs such as Plackett-Burman and factorial design were applied. The fluorescence spectra were treated chemometrically by principal component analysis, linear discriminant analysis and hierarchical cluster analysis to classify the microorganisms according to family, morphology and gram. The best results were obtained using LDA. The method was applied to air samples and the LIF results allowed to characterize bioaerosols reliability. The robustness of the technique was demonstrated by the identification of many bacteria. 相似文献
145.
Raúl Colorado‐Peralta Cristina A. Lpez‐Rocha Sonia A. Snchez‐Ruiz Rosalinda Contreras Angelina Flores‐Parra 《Heteroatom Chemistry》2011,22(1):59-71
The structure and reactivity of a series of new ethylaminedithiazinanes and bis‐diethylaminedithiazinanes synthesized from formaldehyde, NaSH, and N,N‐dimethyl‐ethylene‐diamine ( 1 ), N‐methyl‐ethylene‐diamine ( 2 ), and N‐ethyl‐ethylene‐diamine ( 3 ) are reported. Compound 1 afforded 2‐([1,3,5]‐dithiazinan‐5‐yl)‐ethylene‐N,N‐dimethyl‐amine ( 4 ). The reaction of 4 with dry CH2Cl2 gave N‐{2‐([1,3,5]dithiazinan‐5‐yl)‐ethylene}‐N‐chloromethyl‐N,N‐dimethyl‐ammonium chloride ( 5 ) in high yield, whereas in wet CH2Cl2 and DMSO provided a mixture of 5 with N‐{2‐([1,3,5]‐dithiazinan‐5‐yl)‐ethylene}‐N,N‐dimethyl‐ammonium hydrochloride ( 6 ).bis‐{2‐([1,3,5]‐Dithiazinan‐5‐yl)‐ethylene‐N‐alkyl‐amino}‐methylene‐disulfides ( 7 ) and ( 8 ) formed by two dithiazinanes linked through the chain (CH2)2 NRCH2 S S CH2 NR (CH2)2‐ ( 7 R = methyl, 8 R = ethyl) reacted with CH2Cl2 giving after neutralization of the hydrolysis products the ethylaminedithiazinanes with different pendant N‐groups [ (CH2)2NMeH2+( 9 ); (CH2)2NEtH2+ ( 10 ); (CH2)2NMeH ( 11 ); (CH2)2NEtH ( 12 ); (CH2)2NMeHBH3 ( 13 ) (CH2)2NEtHBH3 ( 14 ). (CH2)2NMe2BH3 ( 15 ), and (CH2)2NEtMeBH3.( 16 )]. The x‐ray diffraction analyses of compounds 5 , 6 , 9 , and 10 are reported. Variable temperature NMR experiments afforded the Δ G≠ of the ring interconversion of the six‐membered heterocycles 6 , 9 , and 10 . © 2010 Wiley Periodicals, Inc. Heteroatom Chem 22:59–71, 2011; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.20657 相似文献
146.
Nylon surface modification: 2. Nylon-supported composite films 总被引:1,自引:0,他引:1
Herrera-Alonso M McCarthy TJ Jia X 《Langmuir : the ACS journal of surfaces and colloids》2006,22(4):1646-1651
We have developed techniques for the introduction of reactive functional groups to nylon surfaces via site-specific reactions targeting at the naturally abundant amide repeating units on the surface. In this report, we describe the fabrication of nylon-supported composite surfaces using the most efficient modification methods we have developed. N-Alkylation with (3-glycidoxypropyl)triethoxysilane (GPTES) in the presence of potassium tert-butoxide (t-BuOK) leads to surfaces with silica-like reactivity. Subsequent chemical vapor deposition using tetrachlorosilane (SiCl4) and water results in composite films with a thin layer of silica, which was made hydrophobic by reaction with a fluorinated silane reagent. Reduction of the amide groups with borane-THF (BH3-THF) complex leads to a 69% conversion of surface amides to the corresponding secondary amine groups. Alginate was chosen as the model polyelectrolyte for the introduction of a hydrated surface layer. Because of the strong electrostatic interaction between alginate and the amine-enriched nylon surfaces, the adsorption is fast and concentration-independent (within the concentration range studied). The polysaccharide coats the surface homogeneously, without the formation of large aggregates. The amine surfaces obtained by reduction with BH3-THF ((BH3-THF)nylon-NH) and by alkylation with 2-bromoethylamine hydrobromide (BEA-HBr, (EBA-HBr)nylon-NH2) were also used to study gold deposition through electroless plating. Immobilization of a negatively charged metal complex (AuCl4(-)) was achieved through electrostatic interaction. Gold particles disperse preferentially in the bulk of (EBA-HBr)nylon-NH2 films, while they remain confined to the outer surface layer of (BH3-THF)nylon-NH films. 相似文献
147.
N-nitrosodimethylamine (NDMA) is a probable human carcinogen of concern that has been identified as a drinking water contaminant. U.S. Environmental Protection Agency Method 521 has been developed for the analysis of NDMA and 6 additional N-nitrosamines in drinking water at low ng/L concentrations. The method uses solid-phase extraction with coconut charcoal as the sorbent and dichloromethane as the eluent to concentrate 0.50 L water samples to 1 mL. The extracts are analyzed by gas chromatography-chemical ionization tandem mass spectrometry using large-volume injection. Method performance was evaluated in 2 laboratories. Typical analyte recoveries of 87-104% were demonstrated for fortified reagent water samples, and recoveries of 77-106% were demonstrated for fortified drinking water samples. All relative standard deviations on replicate analyses were < 11%. 相似文献
148.
U.S. Environmental Protection Agency (EPA) Method 535 has been developed in order to provide a method for the analysis of "Alachlor ESA and other acetanilide degradation products," which are listed on EPA's 1998 Drinking Water Contaminant Candidate List. Method 535 uses solid-phase extraction with a nonporous graphitized carbon sorbent to extract the ethane sulfonic acid (ESA) and oxanilic acid degradates of propachlor, flufenacet, dimethenamid, alachlor, acetochlor, and metolachlor from finished drinking water matrixes. Separation and quantitation of the target analytes are achieved with liquid chromatography/tandem mass spectrometry. Dimethachlor ESA and butachlor ESA were chosen during the method development as the surrogate and internal standard. Drinking water samples were dechlorinated with ammonium chloride without adversely affecting the analyte recoveries. Typical mean recoveries of 92-116% in deionized water and 89-116% in ground water were observed with relative standard deviations of <5%. 相似文献
149.
Margarita Suárez Hector Novoa Yamila Verdecia Amaury Alvarez Rolando Pérez Dolores Molero Norbert M. Blaton Nazario Martín 《Tetrahedron》2006,62(7):1365-1371
Unprecedented 2-iminium chloride salts of 5,8-dihydro-2H-pyrido[3,2-e][1,3]thiazines derivatives (8) were easily synthesized in one step from the corresponding o-chloroformyl-1,4-dihydropyridine (2) and thiourea. The structural study has been carried out by X-ray crystallography and theoretical calculations at the B3LYP/6-31G* levels and reveal that the new salts exhibit appropriate structural features to behave as calcium channel modulators. 相似文献
150.
Glasses in the MoO3-CuO-PbO system are obtained at high cooling rates (104-105 K/s) and characterized using X-ray diffraction (XRD), differential thermal analysis (DTA), infrared (IR) and X-ray photoelectron spectroscopy (XPS). Two glass formation regions are determined: one with compositions having a high MoO3 content (50-80 mol%) and the other in the PbO-rich compositions (65-80 mol%). In the region of MoO3-rich compositions the building units of the amorphous network are МоО6, МоО4 and CuO4 groups. For these high MoO3 contents and respectively low PbO concentrations, the lead oxide is supposed to act as a network modifier while at high content PbO is found to be the main glass network former. In latter case the structure of glasses is formed by chains of PbOn (n = 3, 4) polyhedra, between which there are isolated MoO4 and CuO4 complexes. IR and XPS data reveal the existence of Mo-O-Mo, Mo-O-Me(Me’) (where Me = Cu2+, Cu1+ and Me’ = Pb) and Me(Me’)-O-Me(Me’) bonds in the amorphous network. Surprising result is found for low PbO content (10 mol%) where the lead oxide acts as glass network modifier: the actual MoO3 content drops strongly which is accompanied with a significant increase of the actual CuO content with respect to their nominal MoO3-CuO composition. Such effect is not observed in PbO-rich composition (70 mol%) where PbO has a role of network former. 相似文献