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排序方式: 共有108条查询结果,搜索用时 15 毫秒
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N. Daryabari T. Akbarzadeh M. Amini R. Miri H. Mirkhani A. Shafiee 《Journal of the Iranian Chemical Society》2007,4(1):30-36
The new analogues of nifedipine, in which 2-nitrophenyl group at position 4 is replaced by phenylisoxazolyl substituent, were synthesized. The symmetrical dialkyl 1,4-dihydro-2,6-dimethyl-4-(5-phenylisoxazol-3-yl)pyridine-3,5-dicarboxylates were prepared by classical Hantzsch condensation, and the asymmetrical analogues were synthesized using a procedure reported by Dagnino that involved the condensation of alkyl acetoacetate with alkyl 3-aminocrotonate and 5-phenylisoxazole-3-carboxaldehyde. The structure of all compounds was confirmed by IR, 1H NMR and Mass spectra. In vitro calcium channel antagonist activities were evaluated as calcium channel antagonists using the high K+ concentration of guinea-pig ileum longitudinal smooth muscle (GPILSM) assay. These compounds exhibited moderate calcium antagonist activity (IC50 = 10?7 to 10? 5 M range) relative to the reference drug nifedipine (IC50 = 1.10 ± 0.40 × 10?8 M). 相似文献
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Boumediene Abdellaoui Sofiane E. H. Miri Ireneo Peral Tarik M. Touaoula 《NoDEA : Nonlinear Differential Equations and Applications》2014,21(4):453-490
In this paper we deal with the following quasilinear parabolic problem $$\left\{\begin{array}{l@{\quad}l} (u^\theta)_t - \Delta_p {u} = \lambda \frac{u^{p - 1}}{|x|^{p}} + u^q + f,\,\, u \geq 0 \quad {\rm in} \;\;\Omega \times (0, T),\\ u(x, t) = 0 \quad\qquad\qquad\qquad\qquad\qquad\qquad {\rm on}\; \partial \Omega \times(0, T),\\ u(x, 0) = u_0(x), \,\,\, \qquad\qquad\qquad\qquad\qquad x \in\; \Omega,\end{array}\right.$$ where θ is either 1 or (p ? 1), \({N \geq 3, \,\Omega \subset \mathcal{IR}^N}\) is either a bounded regular domain containing the origin or \({\Omega \equiv \mathcal{IR}^N}\) , 1 < p < N, q > 0 and u 0 ≥ 0, f ≥ 0 with suitable hypotheses. The aim of this work is to get natural conditions to show the existence or the nonexistence of nonnegative solutions. In the case of nonexistence result, we analyze blow-up phenomena for approximated problems in connection with the classical Harnack inequality, in the Moser sense, more precisely in connection with a strong maximum principle. We also study when finite time extinction (1 < p < 2) and finite speed propagation (p > 2) occur related to the reaction power. 相似文献
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The aim of this work is to establish the existence of multi-peak solutions for the following class of quasilinear problems where \(\epsilon\) is a positive parameter, \(N\geq2\), \(V\), \(f\) are continuous functions satisfying some technical conditions and \(\phi\) is a \(C^{1}\)-function.
相似文献
$$ - \mbox{div} \bigl(\epsilon^{2}\phi\bigl(\epsilon|\nabla u|\bigr)\nabla u \bigr) + V(x)\phi\bigl(\vert u\vert\bigr)u = f(u)\quad\mbox{in } \mathbb{R}^{N}, $$
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Pierre Thureau Simone Sturniolo Miri Zilka Fabio Ziarelli Stéphane Viel Jonathan R. Yates Giulia Mollica 《Magnetic resonance in chemistry : MRC》2019,57(5):256-264
Structure determination of functional organic compounds remains a formidable challenge when the sample exists as a powder. Nuclear magnetic resonance crystallography approaches based on the comparison of experimental and Density Functional Theory (DFT)-computed 1H chemical shifts have already demonstrated great potential for structure determination of organic powders, but limitations still persist. In this study, we discuss the possibility of using 13C-13C dipolar couplings quantified on powdered theophylline at natural isotopic abundance with the help of dynamic nuclear polarization, to realize a DFT-free, rapid screening of a pool of structures predicted by ab initio random structure search. We show that although 13C-13C dipolar couplings can identify structures possessing long range structural motifs and unit cell parameters close to those of the true structure, it must be complemented with other data to recover information about the presence and the chemical nature of the supramolecular interactions. 相似文献
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Direct cyanation, using the heterogeneous Friedel-Crafts system cyanogen bromide/aluminium chloride, has given good yields of the following carbonitriles: anthracene-9-, chrysene-6-, 2-methyl-1-naphtho-, 4-methyl-1-naphtho-, 1-naphtho-, phenanthrene-9-, 2,4,6-trimethylbenzo-, triphenylene-1- and triphenylene-2-carbonitriles. 相似文献
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Experiments by Gittings, Bandyopadhyay and Durian (Europhys. Lett. 65, 414 (2004)) demonstrate that light possesses a higher probability to propagate in the liquid phase of a foam due to total
reflection. The authors term this observation photon channelling which we investigate in this article theoretically. We first
derive a central relation in the work of Gitting et al. without any free parameters. It links the photon's path-length fraction f in the liquid phase to the liquid fraction ɛ. We then construct two-dimensional Voronoi foams, replace the cell edges by
channels to represent the liquid films and simulate photon paths according to the laws of ray optics using transmission and
reflection coefficients from Fresnel's formulas. In an exact honeycomb foam, the photons show superdiffusive behavior. It
becomes diffusive as soon as disorder is introduced into the foams. The dependence of the diffusion constant on channel width
and refractive index is explained by a one-dimensional random-walk model. It contains a photon channelling state that is crucial
for the understanding of the numerical results. At the end, we shortly comment on the observation that photon channelling
only occurs in a finite range of ɛ. 相似文献
9.
Molecular adjustment of the electronic properties of nanoporous electrodes in dye-sensitized solar cells 总被引:2,自引:0,他引:2
Rühle S Greenshtein M Chen SG Merson A Pizem H Sukenik CS Cahen D Zaban A 《The journal of physical chemistry. B》2005,109(40):18907-18913
Molecular modification of dye-sensitized, mesoporous TiO2 electrodes changes their electronic properties. We show that the open-circuit voltage (V(oc)) of dye-sensitized solar cells varies linearly with the dipole moment of coadsorbed phosphonic, benzoic, and dicarboxylic acid derivatives. A similar dependence is observed for the short-circuit current density (I(sc)). Photovoltage spectroscopy measurements show a shift of the signal onset as a function of dipole moment. We explain the dipole dependence of the V(oc) in terms of a TiO2 conduction band shift with respect to the redox potential of the electrolyte, which is partially followed by the energy level of the dye. The I(sc) shift is explained by a dipole-dependent driving force for the electron current and a dipole-dependent recombination current. 相似文献
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