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91.
92.
Ruben Dario Fonseca Daniel Souza Correa Elaine Cristina Paris Vinicius Tribuzi Apurba Dev Tobias Voss Pedro Henrique Benites Aoki Carlos Jose Leopoldo Constantino Cleber Renato Mendonca 《Journal of Polymer Science.Polymer Physics》2014,52(4):333-337
We present an approach to fabricate ZnO nanowires/polymer composite into three‐dimensional microstructures, based on two‐photon polymerization direct laser writing, a fabrication method that allows submicrometric spatial resolution. The structural integrity of the structures was inferred by scanning electron microscopy, while the presence and distribution of ZnO nanowires was investigated by energy dispersive X‐ray, Raman spectroscopy, and X‐ray diffraction. The optical properties of the produced composite microstructures were verified by imaging the characteristic ZnO emission using a fluorescence microscope. Hence, such approach can be used to develop composite microstructures containing ZnO nanowires aiming at technological applications. © 2013 Wiley Periodicals, Inc. J. Polym. Sci. Part B: Polym. Phys. 2014 , 52, 333–337 相似文献
93.
An alternative proof of the extended Saalschütz summation theorem for the r + 3Fr + 2(1) series with applications 下载免费PDF全文
Yong S. Kim Arjun. K. Rathie Richard B. Paris 《Mathematical Methods in the Applied Sciences》2015,38(18):4891-4900
A simple proof is given of a new summation formula recently added in the literature for a terminating r + 3Fr + 2(1) hypergeometric series for the case when r pairs of numeratorial and denominatorial parameters differ by positive integers. This formula represents an extension of the well‐known Saalschütz summation formula for a 3F2(1) series. Two applications of this extended summation formula are discussed. The first application extends two identities given by Ramanujan and the second, which also employs a similar extension of the Vandermonde–Chu summation theorem for the 2F1 series, extends certain reduction formulas for the Kampé de Fériet function of two variables given by Exton and Cvijovi? & Miller. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
94.
Minoru Yamaji Cecilia Paris Miguel Ángel Miranda 《Journal of photochemistry and photobiology. A, Chemistry》2010,209(2-3):153-157
A photochemical formation process of avobenzone (AB; 4-tert-butyl-4′-methoxydibenzoylmethane) from 1,1-(4-tert-butybenzoyl)(4′-methoxybenzoyl)butane (PrAB) is studied by steady-state and laser flash photolysis in solution. The quantum yield of the formation via the triplet state of PrAB is determined to be 0.23 in degassed acetonitrile at 295 K. The Arrhenius plots of the decay rate of triplet PrAB show that photoelimination proceeds with an activation energy of 6.0 kcal mol?1 and the frequency factor of 4.6 × 1010 s?1. 相似文献
95.
Fanny Kieken Gaud Pinel Jean-Philippe Antignac Fabrice Monteau Anne Christelle Paris Marie-Agnès Popot Yves Bonnaire Bruno Le Bizec 《Analytical and bioanalytical chemistry》2009,394(8):2119-2128
Despite the worldwide existing regulation banning the use of the recombinant equine growth hormone (reGH) as growth promoter,
it is suspected to be used in horseracing to improve performances. Various analytical methods previously developed to screen
for its misuse have encountered some limitations in terms of detection timeframes, in particular during the first days following
reGH administration. A novel strategy involving the characterization of global metabolomic fingerprints in urine samples of
non-treated and reGH-treated horses by liquid chromatography–electrospray–high-resolution mass spectrometry (LC-ESI-HRMS)
is described and assessed in this paper in order to develop a new screening tool for growth hormone abuse in horseracing.
The strategy involves a limited sample preparation of the urine samples and the use of appropriate software for data processing
and analysis. As preliminary work, reproducibility of both sample preparation and mass spectrometry (MS) measurements was
evaluated in order to demonstrate the reliability of the method. Application of the developed protocol on two horses demonstrated
the suitability of the developed strategy and preliminary results showed significant modifications of the metabolome after
treatment with reGH.
相似文献
96.
Chrétien JM Zammattio F Gauthier D Le Grognec E Paris M Quintard JP 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(26):6816-6828
The preparation of polymer-supported allyltin reagents was shown to be possible for both unfunctionalized and functionalized allyl units. These reagents were treated with aldehydes in the presence of cerium(III) or indium(III) salts to afford high yields of homoallylic alcohols, practically uncontaminated with organotin residues (less than 5 ppm). Some mechanism aspects are briefly discussed and the potential for regeneration and reuse of these supported reagents is pointed out. 相似文献
97.
Paris J Gameiro C Humblet V Mohapatra PK Jacques V Desreux JF 《Inorganic chemistry》2006,45(13):5092-5102
PhenHDO3A is a ditopic ligand featuring a tetraazacyclododecane unit substituted by three acetate arms and one 6-hydroxy-5,6-dihydro-1,10-phenanthroline group (PhenHDO3A = rel-10-[(5R,6R)-5,6-dihydro-6-hydroxy-1,10-phenantholin-5-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid). This ligand was specially designed so as to obtain highly stable heteropolymetallic assemblies. PhenHDO3A has been prepared starting from phenanthroline epoxide and either a triprotected tetraazacyclododecane or tert-butyl triester of N,N',N' '-tetraazacyclododecane-triacetic acid. The latter yields PhenHDO3A in a single step. PhenHDO3A forms kinetically stable lanthanide complexes (acid-catalyzed kinetic constant kH = (1.2 +/- 0.2) x 10(-3) s(-1) M(-1)) whose solution structure has been deduced from a quantitative analysis of the paramagnetic shifts and the longitudinal relaxation times of the proton nuclei of YbPhenHDO3A. The alcohol group of the dihydro-phenanthroline unit remains coordinated to the encapsulated metal ion despite the steric crowding brought about by this group. Furthermore, the complexes are monohydrated, as shown by luminescence lifetime measurements on EuPhenHDO3A solutions. Relaxivity titrations at 20 MHz clearly indicate that the phenanthroline unit of GdPhenHDO3A is available for the spontaneous formation of highly stable tris complexes with the Fe2+ and Ni2+ ions. The water-exchange times and the rotational correlation times of GdPhenHDO3A and Fe(GdPhenHDO3A)32+ have been deduced from variable temperature 17O NMR studies and from nuclear relaxation dispersion curves. Despite rather slow water-exchange rates (taum0 = 1.0-1.2 x 10(-6) s), relaxivity gains of 90% have been observed upon the formation of the heterometallic tris complexes. The latter rotate about four times more slowly (taur0= 398 ps) than the monomeric unit (taur0 = 105 ps) and their relaxivity is, accordingly, twice as high. The relaxivity of the tris complexes between 10 and 50 MHz is comparable to relaxivities reported for Gd3+-containing dendrimers of much higher molecular weights. The high relaxivity of the tris-PhenHDO3A lanthanide complexes is attributed to their internal rigidity. 相似文献
98.
Lithuanian Mathematical Journal - We evaluate a weighted sum of Gauss hypergeometric functions for certain ranges of the argument, weights and parameters. We establish the domain of absolute... 相似文献
99.
13C solid-state nuclear magnetic resonance (NMR) experiments were performed on p-terphenyl, p-quaterphenyl, and p-sexiphenyl either in their pristine or doped with alkali metals form. The 13C NMR spectra of doped materials show new resonances by comparison with pristine compounds. For the K-doped materials, these resonances appear in the 90-135 ppm range, while for Na-doped materials, they are observed in the larger 20-150 ppm range. It suggests that the interaction between the alkali ions and the oligomers depends on the nature of the alkali. It is corroborated by 13C NMR experiments after exposure to air that show different behaviors. As expected, air exposure of K-doped samples restores the pristine spectra. This is not the case for Na doping, where the signature of the doped material persists even after exposure to air. In the latter case, some 13C resonances can be assigned to sp3 hybridized carbons and to the quinoid group. It suggests that Na doping induces a polymerization of the oligophenylenes. 相似文献
100.
When precipitates grow with a lattice misfit inside a matrix having cubic crystal symmetry, a transition may occur from an isotropic arrangement of the precipitates to an alignment along the cubic directions of the crystal. Furthermore, if a uniaxial external strain is applied, an additional transition towards tetragonal symmetry can occur by fusion of the precipitates into large plates perpendicular (or long rods parallel) to the direction of applied strain (“rafting”). Recent experiments on Ni-Al-Mo alloys as well as computer simulations relating to these two transitions are reviewed. 相似文献