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11.
N. A. A. Rossi R. G. Jones S. J. Holder 《Journal of polymer science. Part A, Polymer chemistry》2003,41(1):30-40
ABA block copolymers of methyl methacrylate and methylphenylsilane were synthesized with a methodology based on atom transfer radical polymerization (ATRP). The reaction of samples of α,ω‐dihalopoly(methylphenylsilane) with 2‐hydroxyethyl‐2‐methyl‐2‐bromoproprionate gave suitable macroinitiators for the ATRP of methyl methacrylate. The latter procedure was carried out at 95 °C in a xylene solution with CuBr and 2,2‐bipyridine as the initiating system. The rate of the polymerization was first‐order with respect to monomer conversion. The block copolymers were characterized with 1H NMR and 13C NMR spectroscopy and size exclusion chromatography, and differential scanning calorimetry was used to obtain preliminary evidence of phase separation in the copolymer products. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 30–40, 2003 相似文献
12.
Michaël Lejeune Andrea Valsesia Martin Kormunda Pascal Colpo François Rossi 《Surface science》2005,583(1):L142
In this work, chemically and topographically nanopatterned surfaces were produced by a top-down processing approach for biosensing devices. The nanopatterning was the result of the combination of plasma polymerisation (pp) of biofunctional materials and colloidal lithography techniques. The morphological and chemical properties induced by the plasma deposition-etching treatment were characterised by optical method combining ellipsometry and Fourier Transform Infrared spectroscopy studies. This method supported by atomic force microscopy measurements, allowed the full optical characterization of each step of the top-down process. The optical characterization of the end-up nanopatterned samples demonstrated that the chosen process is able to produce well-defined nanostructured surfaces with controlled chemical and morphological properties. 相似文献
13.
Within the 1/N expansion of O(N) nonlinear σ models for d≤4 it is possible to separate consistently the spin-wave and the massive-mode contributions to the scaling part of the free energy near criticality, and to evaluate them to O(1/N). For critical dimensions d=2+2/n the Abe-Hikami anomaly is recovered, while for d=2 the removal of the spin-wave term is justified. 相似文献
14.
J. P. Leroy J. Micheli G. C. Rossi K. Yoshida 《Zeitschrift fur Physik C Particles and Fields》1990,48(4):653-661
In this paper we present a non-trivial check of the consistency of the quantization of a gauge theory with fermions (QCD) in the temporal gauge. We use the approach based on the finite time Feynman propagation kernel, in which the Gauss law is imposed as a constraint on the states by means of a functional integration over all the time independent gauge transformations acting on the boundary values of the fields. We spell out in detail the “Feynman rules” when fermions are present and we compute, as an example, the gauge invariant correlation function $$\begin{gathered} G(t) = \left\langle {\bar \psi (0,t)(\gamma _5 \gamma _0 )\frac{{1 - \gamma _0 }}{2}P} \right. \hfill \\ \left. { \cdot \exp \left( {ig\int\limits_0^t {A_0 (0,t')dt'} } \right)(\gamma _5 \gamma _0 )^ + (0,0)} \right\rangle \hfill \\ \end{gathered} $$ up to orderg 2, obtaining the expected result. 相似文献
15.
16.
Simultaneous separation and identification of hashish constituents by coupled liquid chromatography-mass spectrometry (HPLC-MS) 总被引:1,自引:0,他引:1
C. Rustichelli V. Ferioli F. Vezzalini M. C. Rossi G. Gamberini 《Chromatographia》1996,43(3-4):129-134
Summary This paper reports the use of liquid chromatography for the separation and determination of the major cannabinoids extracted from hashish samples. The direct coupling to the mass spectrometer enables the selective identification both of neutral and acidic cannabinoids. The developed method does not require any preliminary derivatization and should, therefore, be of interest in forensic analysis for simple and unequivocal determination of hashish constituents.Part of this work was presented at the 2nd Italian-Spanish Joint Meeting of Medicinal Chemistry, 30 August–3 September 1995, Ferrara, Italy. 相似文献
17.
Giampiero Bettinetti Milena Sorrenti Laura Catenacci Franca Ferrari Silvia Rossi Ilaria Salvadeo Paolo Carraro 《Journal of inclusion phenomena and macrocyclic chemistry》2007,57(1-4):329-332
Triacetyl α-cyclodextrin, triacetyl β-cyclodextrin and triacetyl γ-cyclodextrin were tested as possible hydrophobic carriers
to prolong the release of hydrophilic teicoplanin (TCP). Physical–chemical characterization of individual components, drug-carrier
physical mixtures at 0.5, 0.67 and 0.75 mass fraction of carrier, and the respective interaction products by kneading or evaporative
crystallization under microwave irradiation was carried out using differential scanning calorimetry (DSC) and thermogravimetric
analysis (TGA). In vitro drug release in pH 7.4 phosphate buffer at 37 °C was determined by intrinsic dissolution rate (IDR)
measurements on non disintegrating compressed discs. Solid-state interactions of TCP with triacetyl α-cyclodextrin by evaporative
crystallization and kneading and with triacetyl β-cyclodextrin by evaporative crystallization (probably resulting in carrier
amorphization) were demonstrated. The role of carrier hydrophobicity, carrier mass fraction and preparation method of solid
drug-carrier combinations on solid-state drug-carrier interactions and slowing down of TCP release was assessed. Modulation
of drug release can be achieved using TCP-triacetyl γ-cyclodextrin combinations at 0.5 mass fraction of carrier. 相似文献
18.
19.
Roubin P Chandesris D Rossi G Lecante J Desjonquères MC Tréglia G 《Physical review letters》1986,56(12):1272-1275
20.
Stefano Vecchio Alessia Catalani Vanessa Rossi Mauro Tomassetti 《Thermochimica Acta》2004,420(1-2):99-104
The thermal behaviour of acetanilide (Ac) and two of its analogues, namely the para-ethoxyacetanilide (p-Eto Ac) and the para-bromoacetanilide (p-Br Ac), which are used as analgesics in the pharmaceutical industry was studied with a simultaneous TG/DSC unit. The examined analgesics showed two endothermic DSC peaks due to melting and vaporization. By combining the experimental TG data with the corresponding reference vapour pressure data obtained with the Antoine equation the plot of P versus v was derived. From the slope of this equation the constant k-value was determined for Ac. Then, using the same k-value the vapour pressures of p-Eto Ac and p-Br Ac were determined in the same temperature range. The vaporization enthalpies for all the studied compounds were obtained from different methods and a very good agreement was found. Vaporization follows a zero-order kinetics. The activation energy of vaporization (Evap) was calculated from the dynamic TG experiments, using the Arrhenius equation. 相似文献