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41.
Y. Chushkin F. Zontone E. Lima L. De Caro P. Guardia L. Manna C. Giannini 《Journal of synchrotron radiation》2014,21(3):594-599
The progress of tomographic coherent diffractive imaging with hard X‐rays at the ID10 beamline of the European Synchrotron Radiation Facility is presented. The performance of the instrument is demonstrated by imaging a cluster of Fe2P magnetic nanorods at 59 nm 3D resolution by phasing a diffraction volume measured at 8 keV photon energy. The result obtained shows progress in three‐dimensional imaging of non‐crystalline samples in air with hard X‐rays. 相似文献
42.
M.T.S. Alcântara A.J.C. Brant D.R. Giannini J.O.C.P. Pessoa A.B. Andrade H.G. Riella A.B. Lugão 《Radiation Physics and Chemistry》2012,81(9):1465-1470
In this work several hydrogels were obtained with two different poly(vinyl alcohol)s/PVAs as the main polymer in aqueous solutions containing 10% of PVA, 0.6% of agar, and 0.6% of κ-carrageenan (KC), cross-linked by gamma-rays from a 60Co irradiation source. The PVAs tested have different degrees of hydrolysis and viscosities at 4% with values closed to 30 mPa s. The aqueous polymeric solutions were prepared using two distinct processes: the simple process of heating–stirring and that of making use of an autoclave. The purpose of this study was to evaluate the influence of the dissolution process by means of both methods on the hydrogels’ properties obtained. These were investigated by means of degree of cross-linking/gel fraction, degree of swelling in water, and some mechanical properties. The results that are obtained for hydrogels synthesized from solutions of PVA, agar, KC, and blends thereof prepared by both dissolution processes showed higher degrees of swelling for hydrogels from the autoclaved polymer solutions than those from the solutions prepared by simple heating–stirring process. Furthermore, their hydrogels containing totally hydrolyzed PVA displayed higher tensile strength and lower elongation properties. 相似文献
43.
Pietro Tundo Alvise Perosa Maurizio Selva Ludovico Valli Cinzia Giannini 《Colloids and surfaces. A, Physicochemical and engineering aspects》2001,190(3):295-303
A new amphiphilic derivative of fullerene C60 bearing an oligoglycyl tail (C60CHCOgly2OEt, 2) formed stable Langmuir floating films at the air–water interface. This occurred when the molecular assembly was stabilized by anchoring the amphiphilic C60's to the aqueous subphase, via hydrogen bonding interactions between a dipeptide (Gly–L–Leu) dissolved in the water subphase, and the oligoglycyl chain. The compression (π−A) isotherm of the Langmuir floating film constructed in such a way showed no hysteresis, was steep, and evidenced that the monolayer collapsed at a surface pressure π65 mN m−1, thus confirming that the film was tightly packed, extremely stable, and rigid. A limiting area per molecule of 89.1 Å2 was extrapolated, in agreement with the calculated cross-section area of the C60 fullerene. On the contrary, when the dipeptide was absent and pure water was used as the subphase, the π−A isotherm yielded a limiting area <55 Å2 which indicated the formation of multiple layers; moreover it showed significant hysteresis, the film was fragile, and it collapsed at π≈50 mN m−1. Once anchored by the dipeptide, the floating monolayer of 2 could be transferred onto hydrophobic quartz, glass and silicon substrates, by successive vertical dipping cycles, each cycle made up of two down-strokes and two up-strokes, to yield the Langmuir–Blodgett film. Up to 200 down- and up-strokes could be repeated reproducibly, a noteworthy result for non-covalently assembled LB films of fullerenes. The transfer ratio was 1.0, except for the second down-stroke of each cycle that gave a transfer ratio of zero, making the sequence of successful transfers: D, U, U, (cleaning and spreading), D, U, U, (cleaning and spreading), and so on (D=down-stroke, U=up-stroke). The total number of deposited layers was therefore 150. X-ray diffraction spectra were registered and exhibited a peak, which was fitted by a Montecarlo method of simulation to obtain the distribution of the repeat unit responsible for scattering; such distribution, with thickness between 20 and 60 Å, was consistent with the size of the amphiphile and the transfer sequence. The UV–Vis spectra of the LB film exhibited the characteristic C60 bands, and the absorption peaks in the 200–400 nm range were proportional to the number of layers, indicating that the deposition was reproducible and that the molecular environment of C60 in each layer remained constant. 相似文献
44.
Enrico Albizzati Umberto Giannini Gianpiero Morini Maurizio Galimberti Luisa Barino Raimondo Scordamaglia 《Macromolecular Symposia》1995,89(1):73-89
The role of Lewis bases in MgCl2 supported catalysts for olefin polymerization is a subject of continuous interest and discussion in order to obtain more and more active and stereospecific catalysts and to explain their stereoregulating mechanism. Through molecular calculation and conformational analysis it was possible to identify chelating diethers that have the correct oxygen-oxygen distance necessary to tightly coordinate with the Mg ions of the support, even in the presence of other strong Lewis acids, and unable to give secondary reactions with TiCl4, AlR3, Ti-C and Ti-H bonds. The use of these donors has allowed the synthesis of catalytic systems that are both highly active and stereospecific even in the absence of external donors. Kinetic data of propylene polymerization with these catalyst systems are reported. The importance of the distance between the donor atoms in bifunctional Lewis bases has been proved also in the case of new classes of internal donors. Molecular modelling studies have enabled us to formulate models of active sites, located on some corners of MgCl2 crystallites, whose chirality is induced by the presence of a donor molecule in their environment. These models could explain, at least in part, the exceptional increase of isotactic polymer productivity observed for stereospecific catalyst systems, containing only the internal donor, with respect to catalysts lacking the Lewis base and could account for the influence of the donor on the molecular properties of the obtained polymers. 相似文献
45.
46.
The influence of Δ degrees of freedom on the energy-weighted M1 sum rule is investigated and applied to 2H and 4He. Using π- and ρ-exchange potentials a reduction of the potential contribution of the order of 50% is obtained. The absolute value of the sum rule is strongly dependent on the short-range behaviour of the nuclear wave function. Furthermore, the contribution of c.m. effects is evaluated and found to be of the order of 5–10%. 相似文献
47.
48.
Stefano Maiorana Antonio PapagniEmanuela Licandro Rita AnnunziataPiero Paravidino Dario PerdicchiaClelia Giannini Marco BenciniKoen Clays André Persoons 《Tetrahedron》2003,59(34):6481-6488
This paper describes a convenient preparation of tetrathia-[7]-helicene (TH[7]), the generation of the α-anion on the terminal thiophene ring, and the synthesis of the 2-formyl-tetrathia-[7]-helicene (2-CHO-TH[7]). The key intermediate trans-1,2-dibenzodithiophene-ethene, prepared in 97% yield by McMurry coupling of the 2-formyl-benzo[1,2-b;4,3-b′]dithiophene, was transformed into TH[7] using a known procedure. The described method affords TH[7] in 46% overall yield, which is more than four times the yield previously reported in the literature. The α-anion of TH[7], which is easily generated on the α-position of one of the terminal thiophene rings, reacts with electrophilic reagents such as D2O and DMF. The latter reaction proved to be the best way to prepare 2-CHO-TH[7], a key intermediate for the preparation of new substituted heterohelicenes. 相似文献
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50.