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991.
The preparation of polymer microcapsules of well defined size in the range of 10–50 μm with different shell thickness to
core diameter ratios is described. An aerosol of monodisperse droplets of a homogeneous ternary liquid system which contained
a hydrophobic component and a hydrophilic component dissolved in a high-volatile mutual solvent, was produced by dispersing
with a vibrating-orifice aerosol generator. After the evaporation of the solvent in a nitrogen atmosphere the particles demix
and form a two-phase droplet of core-shell type. These droplets were illuminated with UV light and polymerized to highly monodisperse
microcapsules with a solid polymer shell and a liquid core. The properties of the resulting particles (size, size distribution,
shell thickness, shape and surface characteristics) were investigated by scanning electron microscopy, Raman spectroscopy
on single optically levitated particles, and confocal Raman micro spectroscopy. The microcapsules were highly monodisperse
and have spherical shape.
Received: 24 July 1996 Accepted: 29 August 1996 相似文献
992.
In this review, thin films of SiO2 on Mo(1 1 2) and MgO(1 0 0) on Mo(1 0 0) have been characterized using metastable impact electron and ultraviolet photoelectron spectroscopies (metastable impact electron spectroscopy (MIES) and ultraviolet photoelectron spectroscopy). The electronic and chemical properties of the thin films are identical to those of the corresponding bulk oxides. For different prepared defective SiO2 surfaces, additional features are observed in the band-gap region. These features arise from vacancies or excess oxygen and are consistent with theoretical predictions of additional occupied states in the band-gap due to point defects. Extended defect sites on SiO2 and MgO are identified using MIES by a narrowing of the O(2p) features with a reduction in the density of extended defect sites. MIES of adsorbed Xe (MAX) is also used to estimate the density of extended defect sites. Furthermore, it is shown that CO is an appropriate probe molecule for estimating the defect density of MgO surfaces. Upon Ag exposure, the change in the work function of a low defect MgO(1 0 0) versus a high defect surface is markedly different. For a sputter-damaged MgO(1 0 0) surface, an initial decrease of the work function was found, implying that small Ag clusters on this surface are electron deficient. In contrast, for SiO2 no significant change of the work function upon Ag exposure with increasing defect density was observed. On MgO(1 0 0), the presence of defect sites markedly alter the electronic and chemical properties of supported Ag clusters. Such a strong influence of defect sites was not found for Ag clusters on SiO2. 相似文献
993.
The mechanism of photooxidation of phenothiazine in liquid and frozen (77 K) aqueous micellar solutions of the surfactant (sodium dodecyl sulfate) was studied by ESR. The main reaction of electrons formed by the photochemical oxidation of phenothiazine in a liquid micellar solution of the anionic surfactant is the reduction of molecular oxygen dissolved in the aqueous bulk phase. 10-Methylphenothiazine was used as a stable radical cation probe in a liquid solution. The influence of electrolytes on the photoionization yield in both frozen and liquid solutions of the surfactant was studied. 相似文献
994.
Investigation of the Interactions of β‐Peptides with DNA Duplexes by Circular Dichroism Spectroscopy
Kenji Namoto James Gardiner Thierry Kimmerlin Dieter Seebach 《Helvetica chimica acta》2006,89(12):3087-3103
The interaction of β‐peptides with the DNA duplexes of dA20dT20 and a GCN4‐binding CRE sequence was examined. To gauge the factors that govern these interactions, two β‐pentadecapeptides, 1 and 2 , a β‐dodecapeptide, 3 , three β‐decapeptides, 4 – 6 , three β‐heptapeptides, 7 – 9 , and β‐octaarginine 10 were designed and synthesized. The β‐peptides were conceived to adopt a β‐peptide 314 helix, in which the side chains at position i and i + 3 are aligned vertically along one side of the helix. The side chains of Lys, Asn, and Arg were positioned such that potential H‐bonding sites were created for a helical conformation to interact with the base pairs of DNA. CD Analysis showed that β‐peptides 1, 2 , and 10 interacted with dA20dT20. In addition, β‐peptides 1 and 2 showed significant interaction with a DNA‐duplex 20mer containing the ATF/CREB recognition sequence for the regulatory protein GCN4. It is impossible, at this stage of the investigation, to make a safe proposal about the actual nature of the interaction of the structures(s) of the complexes, the formation of which is suggested by the CD spectra reported herein. 相似文献
995.
996.
D. L. Lipilin A. M. Churakov Yu. A. Strelenko V. A. Tartakovsky 《Russian Chemical Bulletin》2007,56(8):1566-1568
Treatment of 2-(tert-butyl-NNO-azoxy)anilines with phosgene at 20 °C was proposed as a novel route to 1,2,4-benzotriazin-3(4H )-one 1-oxides. This method involves a new reaction, viz., an intramolecular interaction of the tert-butyl-NNO-azoxy group with a C-electrophile (leading to the formation of the N(2)—C(3) bond of the triazine ring) followed by elimination
of the tert-butyl group. Complete assignment of the signals in the 1H and 13C NMR spectra of the compounds obtained was performed.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1507–1509, August, 2007. 相似文献
997.
Shul"gin V. F. Zlatogorskii S. M. Zub V. Ya. Larin G. M. 《Russian Chemical Bulletin》2002,51(12):2273-2276
The binuclear vanadyl(ii) complexes [(VO)2·2Py·2EtOH]·mH2O with acyldihydrazones of salicylaldehyde (H4L) and dicarboxylic acids were synthesized and studied. In these complexes, two chelate vanadyl(ii) complexes with the tridentate bicyclic ligands are linked to each other by the polymethylene bridges —(CH2)
n
— of different lengths varying from one to four units. The ESR spectra of solutions of these complexes, unlike those of analogous copper(ii) complexes, have an isotropic signal with an eight-line hyperfine structure (g = 1.972, a
V = 93·10–4 cm–1) typical of monomeric vanadyl complexes, which indicates that no exchange interactions occur between the paramagnetic centers through the polymethylene chain. 相似文献
998.
Hossein?EshghiEmail author Sayyed Faramarz?Tayyari Esmaiel?Sanchuli 《Monatshefte für Chemie / Chemical Monthly》2004,135(9):1101-1111
Summary. The regioselective ring opening of epoxides using elemental iodine and bromine in the presence of o-phenylenediamine as a new catalyst affords vicinal iodo alcohols and bromo alcohols in high yields. The major advantages of this method are versatility, high regioselectivity, a cheap and commercially available catalyst, mild and neutral reaction conditions, and short reaction times. Fourier transform Raman spectroscopy was used to study the reaction of iodine with o-phenylenediamine. The results indicate that the complex [(Diamine)I]+·I5– is formed, and we suggest that the major nucleophile is the pentaiodide ion. This bulky nucleophile has a fundamental role in the high regioselectivity observed attacking the less sterically hindered epoxide carbon. 相似文献
999.
1000.
A single crystal of a new sodium calcium iron (III) phosphate, Na4CaFe4(PO4)6, has been synthesized by a flux method and characterized by X-ray diffraction, Mössbauer spectroscopy and magnetic susceptibility measurements. The compound crystallizes in the monoclinic space group C2/c(a=12.099(5) Å, b=12.480(5) Å, c=6.404(2) Å, β=113.77(3)°, Z=2, R1=0.022, Rw2=0.066). The crystal structure belongs to the alluaudite type, characterized by the X(2)X(1)M(1)M(2)2(PO4)3 general formula. The open framework results from Fe2O10 units of edge-sharing FeO6 octahedra, which alternate with M(1)O6 octahedra (M(1)=Na+Ca) that form infinite chains. These chains are linked together through the common corners of PO4 tetrahedra yielding two distinct tunnels of sodium cation occupation. This compound is antiferromagnetic with a Néel temperature of 35 K. Mössbauer parameters are consistent with the structural results. 相似文献