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141.
Amir Behzadnia Majid Montazer Abousaeid Rashidi Mahnaz Mahmoudi Rad 《Photochemistry and photobiology》2014,90(6):1224-1233
Nano nitrogen‐doped titanium dioxide was rapidly prepared by hydrolysis of titanium isopropoxide at 75–80°C using in situ sonochemical synthesis by introducing ammonia. Various concentrations of titanium isopropoxide were examined to deposit nano nitrogen‐doped titanium dioxide through impregnation of the wool fabric in ultrasound bath followed by curing. The antibacterial/antifungal activities of wool samples were assessed against two common pathogenic bacteria including Escherichia coli and Staphylococcus aureus and the diploid fungus Candida albicans. The sonotreated wool fabrics indicated no adverse effects on human dermal fibroblasts. The presence of nanoparticles on the sonotreated wool fabrics were confirmed by FE‐SEM images and EDS patterns and X‐ray mapping and the crystalline size of nanoparticles were estimated through XRD results. The role of both pH and precursor concentration on the various properties of the fabric was investigated and the optimized conditions introduced using response surface methodology. 相似文献
142.
In this paper, we introduce a general modeling approach for the crosstalk phenomenon within electro-magnetic systems. We model the phenomenon by bilateral coupling of two sets of differential equations, namely non-stationary Maxwell equations and circuit equations. Considering these two sets of equations as input-output systems, the bilateral coupling approach connects the output of one system to the input of the other system and conversely, via coupling and re-coupling relations. The coupling of these two sets leads to a set of partial differential-algebraic equations modeling the crosstalk phenomenon. (© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
143.
p‐Toluenesulfonic acid catalyzed the one‐pot, three‐component synthesis of 3‐aminoimidazo[1,2‐a]pyridines and pyrazines through a condensation reaction of a 2‐aminoazine, an aldehyde, and an isocyanide at room temperature. This methodology affords a number of 3‐aminoimidazo[1,2‐a]pyridines in reasonable yields and short reaction times without any significant optimization of the reaction conditions. 相似文献
144.
On Thiomercurates. 3. About BaHgS2 The hitherto unknown carminred BaHgS2 was prepared by heating binary sulfides [intimate mixtures, Ba:Hg = 1.00:1, in quartz-seales, 600–650°C, 2–3 d (powder), or 700–750°C, 8–10 d (single crystals)]. BaHgS2 crystallizes orthorhombic with a = 4.215, b = 14.388, c = 7.338 Å, space group Pmc21. The new structure was elucidated by diffractometer data (MoKα), 1199 of 1228 independent hkl, R = 8.8, RW = 9.2% as final result (Parameter see text). Effective Coordination Numbers, ECoN, Mean Fictive Ionic Radii, MEFIR, and the Madelung Part of Lattice Energy, MAPLE are discussed. 相似文献
145.
F. Radó 《Archiv der Mathematik》1969,20(3):311-319
Ohne Zusammenfassung 相似文献
146.
Mohammad Navid Soltani Rad Ali Khalafi-Nezhad Mohammad Ali Faghihi Abolfath Parhami 《Tetrahedron》2008,64(8):1778-1785
A convenient and efficient one-pot N-alkylation of nucleobases from alcohols using N-(p-toluenesulfonyl)imidazole (TsIm) is described. In this method, treatment of alcohols with a mixture of purine or pyrimidine nucleobase, TsIm, K2CO3, and triethylamine in refluxing DMF regioselectively furnishes the corresponding N-alkyl nucleobases in good yields. This methodology is highly efficient for various structurally diverse primary alcohols. 相似文献
147.
A highly stereoselective method for preparing ( Z)- and ( E)-enol triflates derived from substituted acetoacetate derivatives is described. The salient feature of this methodology is the use of Schotten-Baumann-type conditions to control enolate geometry using either aqueous LiOH ( Z-selective) or aqueous (Me)(4)NOH ( E-selective) in combination with triflic anhydride to provide a practical and predictable approach to these valuable substrates. 相似文献
148.
Farideh Namvar Susan Azizi Rosfarizan Mohamad Amin Boroumand Moghaddam Mozhgan Soltani Fazele Moshfegh 《Research on Chemical Intermediates》2016,42(3):1571-1581
Palm pollen (PP) has been widely used in nutrition, pharmaceutical and cosmetic industries. In the present study, we explored the potential of PP in the synthesis of a silver nanoparticle (Ag NP). PP was used as both reducing and stabilizing agent. The Ag/PP nanocomposite was examined by field emission electron microscopy, X-ray diffraction, Fourier transform infrared (FT-IR) spectroscopy, ultraviolet spectroscopy and zeta potential measurement. The biosynthesized NPs showed surface plasmon resonance centered at 425 nm with an average particle size measured to be 23 nm and a zeta potential of ?30.9 mV. Prominent FT-IR signals were obtained and ascribed to phenolic and carbohydrate compounds involved in the formation of the Ag NPs, and proteins which participated in stabilization of the Ag NPs. The biologically synthesized Ag NPs were found to be extremely effective against E. coli (13.8 ± 0.25 mm) with a minimum inhibitory concentration of 20 µg/mL. Thus, such biosynthesized Ag NPs can be used in medicinal applications. 相似文献
149.
The maximum nullity over a collection of matrices associated with a graph has been attracting the attention of numerous researchers for at least three decades. Along these lines various zero forcing parameters have been devised and utilized for bounding the maximum nullity. The maximum nullity and zero forcing number, and their positive counterparts, for general families of line graphs associated with graphs possessing a variety of specific properties are analysed. Building upon earlier work, where connections to the minimum rank of line graphs were established, we verify analogous equations in the positive semidefinite cases and coincidences with the corresponding zero forcing numbers. Working beyond the case of trees, we study the zero forcing number of line graphs associated with certain families of unicyclic graphs. 相似文献
150.
Scandium,yttrium, and ytterbium bisalkyl complexes stabilized by monoanionic amidopyridinate ligands
D. M. Lyubov V. Yu. Rad’kov A. V. Cherkasov G. K. Fukin A. A. Trifonov 《Russian Chemical Bulletin》2016,65(11):2594-2600
A reaction of Sc, Y, and Yb amidopyridinate dichlorides with the corresponding amount of LiCH2SiMe3 was used to synthesize bis(trimethylsilylmethyl) complexes (Ap)Ln(CH2SiMe3)2-(THF) (Ap is N-mesityl-6-(2,4,6-triisopropylphenyl)pyridine-2-amide (Ap9Me), Ln = Y (2); Ap is N-(2,6-diisopropylphenyl)-6-(2,4,6-triisopropylphenyl)pyridine-2-amide (Ap*), Ln = Sc (3), Yb (4)). An exchange reaction of yttrium amidopyridinate dichloride derivative 1 with 4 equiv. of ButLi in hexane gave the corresponding di-tert-butyl derivative Ap9MeY(But)2(THF) (5). Molecular structures of complexes 3 and 4 were established by X-ray diffraction. A method of the ligand solid angles was used to calculate the completion degree of the metal atom coordination sphere for the series of isomorphic derivatives (Ap*)Ln(CH2SiMe3)2(THF) containing the central metal ions with different ionic radii (Sc, Y, Yb, Lu). According to this method, the amidopyridinate ligand solid angle in these complexes virtually does not vary, while the solid angles of coordinated THF molecule and alkyl ligands vary within a wide range. 相似文献