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91.
Pasquale Longo Alfonso Grassi Fabia Grisi Stefano Milione 《Macromolecular rapid communications》1998,19(5):229-233
1-Vinylcyclohexene was polymerized in the presence of several homogeneous catalytic systems consisting of methylaluminoxane and group 4 metallocenes such as CpTiCl3, [isopropyl(cyclopentadienyl)(1-fluorenyl)]ZrCl2,rac-[ethylenebis(1-indenyl)] ZrCl2, (CH3)2Si(Cp)2ZrCl2, CpZrCl3. The structure of the polymers depends on the catalyst. In fact, with CpTiCl3, [isopropyl(cyclopentadienyl)(1-fluorenyl)]ZrCl2 and rac-[ethylenebis-(1-indenyl)]ZrCl2 the polymers are chemo-, regio- and stereoregular with 1,4 cis, 1,4 trans and 1,2 isotactic structure, respectively. 相似文献
92.
Pasquale Blasi 《Brazilian Journal of Physics》2014,44(5):426-440
The last decade has been dense with new developments in the search for the sources of Galactic cosmic rays. Some of these developments have confirmed the tight connection between cosmic rays and supernovae in our Galaxy, through the detection of gamma rays and the observation of thin non-thermal X-ray rims in supernova remnants. Some others, such as the detection of features in the spectra of some chemicals, opened new questions on the propagation of cosmic rays in the Galaxy and on details of the acceleration process. Here, I will summarize some of these developments and their implications for our understanding of the origin of cosmic rays. I will also discuss some new avenues that are being pursued in testing the supernova origin of Galactic cosmic rays. 相似文献
93.
94.
Rolf Holderegger Luigi M. Venanzi Fiorella Bachechi Pasquale Mura Luigi Zambonelli 《Helvetica chimica acta》1979,62(7):2159-2167
The preparation of the nucleophile trans-[RuCl(NO)( 1 )], where 1 is the bidentate ligand Ph2PCH2C18CH2PPh2, and of the five-coordinate species [RuCl(CO)(NO)( 1 )], [RuCl(CO)(NO)(Ph2PCH2Ph)2] and [RuCl(NO)( 2 )( 1 )] are reported. The crystal structure of [RuCl(CO)(NO)( 1 )] shows that the coordination around the metal atom is distorted trigonal bipyramidal with the phosphorus atoms in axial positions. The Ru? N? O bond angle is 142.8°. 1H- and 31P-NMR. and \documentclass{article}\pagestyle{empty}\begin{document}$ \tilde \nu $\end{document}NO IR.-data for the above complexes are reported and related to the coordination geometry. 相似文献
95.
K. B. Wiles V. A. Bhanu A. J. Pasquale T. E. Long J. E. McGrath 《Journal of polymer science. Part A, Polymer chemistry》2004,42(12):2994-3001
Nonlinear monomer reactivity ratios for the homogeneous free‐radical copolymerization of acrylonitrile and methyl acrylate were determined from 1H NMR and real‐time Fourier transform infrared (FTIR) analyses. All 1H NMR data were obtained on polymers isolated at low conversions (<10%), whereas the FTIR data were collected in situ. The copolymerizations were conducted in N,N‐dimethylformamide at 62 °C and were initiated with azobisisobutyronitrile. The real‐time FTIR technique allowed for many data points to be collected for each feed composition, which enabled the calculation of copolymer compositions (dM1/dM2) with better accuracy. Monomer reactivity ratios were estimated with the Mayo–Lewis method and then were refined via a nonlinear least‐squares analysis first suggested by Mortimer and Tidwell. Thus, monomer reactivity ratios at the 95% confidence level were determined to be 1.29 ± 0.2 and 0.96 ± 0.2 for acrylonitrile and methyl acrylate, respectively, which were valid under the specific system conditions (i.e., solvent and temperature) studied. The results are useful for the development of acrylonitrile (<90%) and methyl acrylate, melt‐processable copolymer fibers and films, including precursors for carbon fibers. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2994–3001, 2004 相似文献
96.
We introduce a procedure which transforms a given incidence structure into another one, provided certain conditions are met.Work performed under the auspices of GNSAGA of CNR supported by the 40% and 60% grants of MURST. 相似文献
97.
98.
99.
Pasquale Curcio Christelle Zandanel Alain Wagner Charles Mioskowski Rachid Baati 《Macromolecular bioscience》2009,9(6):596-604
This paper describes a new type of surface imprinting technique that combines the advantages of both the semi‐covalent approach and one‐stage miniemulsion polymerization. This process has been successfully applied for the preparation of glucose surface‐imprinted nanoparticles. The selective artificial receptors for glucopyranoside were fully characterized by IR, TEM and BET analyses, and their molecular recognition abilities by binding experiments carried out in batch processes. The molecular affinity and selectivity of the glucose molecularly imprinted polymers were accurately quantified. These characteristics are essential for verification of the efficiency of the developed surface imprinting process. The imprinting effect was clearly demonstrated using the batch rebinding method. We have found that the glucose imprinted polymers produced using the optimized one‐stage mini‐emulsion exhibited quite fast kinetics of binding and equilibration with glucopyranoside templates, compared to polymers prepared by bulk polymerization technique, as well as extremely low levels of unspecific bindings. We also demonstrated that glucose molecular imprinted polymer (MIP) exhibited very good selectivity for its original template compared to other glycopyranoside derivatives, such as galactose. Finally, the extraction of the binding properties from isotherms of binding by fitting to the bi‐Langmuir and Freundlich models allowed the determination of the affinity constant distribution of the binding sites. This imprinting protocol allowed the determination of an affinity constant (KD), involving exclusively H‐bonding interactions, for the glucose MIP ( P2C ) with the best template 1 , in CH3CN as the solvent system.
100.
Rodríguez Nieto FJ Pasquale MA Cabrera CR Arvia AJ 《Langmuir : the ACS journal of surfaces and colloids》2006,22(25):10472-10482
The topography of platinum electrodes produced by electrodeposition (19 to 200 mC cm-2) on highly oriented pyrolytic graphite (HOPG) under different potential modulations was investigated by atomic force microscopy, scanning tunneling microscopy, and H-atom electrosorption voltammetry. To modulate electrodeposition, (i) triangular potential cycling at 0.1 V s-1, (ii) a linear cathodic potential at 0.1 V s-1 and anodic potential step cycling, and (iii) square wave potential cycling at 5000 Hz were utilized. AFM and STM imaging showed that at lower platinum loading the HOPG surface was partially covered by a 3D sublayer of platinum. Electrodes produced by procedure (i) were made of faceted platinum aggregates of about 200 nm and nanoclusters in the range of 5-20 nm; those that resulted from procedure (ii) consisted of anisotropic aggregates of nanoclusters arranged as quasi-parallel domains. These electrodes from (i) and (ii) behaved as fractal objects. The electrodes resulting from procedure (iii) exhibited a flat surface that behaved as a Euclidean object. For all WEs, as the platinum loading was increased the HOPG surface was fully covered by a thin 3D layer of platinum aggregates produced by electrodeposition and coalescence phenomena. Large platinum loading led to electrodes with fractal geometry. Statistical parameters (root-mean-square height, skewedness, kurtosis, anisotropy, Abbot curve, number of protrusions and valleys, and fractal dimension) were obtained from the analysis of AFM and STM imaging data. Platinum electrodeposition coupled to either H-adatom formation for procedures (i) and (ii) or phonon dispersion for (iii) was involved in the surface atom rearrangements related to electrofaceting. The H-adatom electrosorption voltammetry data were used to evaluate the real electrode surface area via the voltammetric charge and to advance a tentative explanation of the contribution of the different crystallographic facets to the global electrochemical process dominated by weak H-Pt adsorption interactions. 相似文献