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101.
Masao Kato Takao Shiraga Tatsumi Kimura Takashi Fukuda Hiro Matsuda Hachiro Nakanishi 《先进技术聚合物》2002,13(2):120-126
We synthesized some novel rigid NLO‐active maleimide copolymers bearing DR‐1 moieties ( PMPD , PHSD and PHND ). All copolymers exhibited high Tg's (190~197 °C), good solubilities for common solvents and excellent film‐forming properties. Dependence of film thickness on the d33 value for the poled copolymer films induced by corona poling was investigated and it was demonstrated that in less than thickness of 0.3 µm decrease of the thickness gives rise to remarkable increase in the d33 value. The poled copolymer films exhibited large d33 values (270 × 10?9 esu (film thickness 0.13 µm) for PMPD , 290 × 10?9 esu (0.12 µm) for PHSD and 350 × 10?9 esu (0.08 µm) for PHND ) as well as large r33 values (51.0 pmV?1 for PMPD and 60.4 pmV?1 for PHND ) which are significantly large compared to the value of LiNbO3 (31 pmV?1) as a typical EO material. The d33 values of the poled copolymers were kept constant even after standing 1000h at 80 °C, although a small decrease was observed at an initial stage. Further, the d33 values did not change up to ca. 123 °C upon heating at the rate of 10 °C/min in all cases. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
102.
Based on experimental data about the density of very dilute solutions of H2O and D2O in 1,4-dioxane, hexamethylphosphotriamide, and acetonitrile at 278.15 K-318.15 K we determined the limiting partial molar volume (error ±0.03 cm3·mol−1) and dilatability of the water component. A correlation equation has been derived which relates the isotope effect (IE) in the limiting excess partial molar dilatability of water to the energy of the H2O-solvent hydrogen bond. The stated IE may be used as a “structural indicator” for evaluating the ability of an aprotic dipolar solvent to undergo specific interactions through hydrogen bonding.Original Russian Text Copyright © 2004 by E. V. Ivanov, V. K. Abrosimov, and E. Yu. Lebedeva__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 6, pp. 1020–1026, November–December, 2004. 相似文献
103.
The solid state thermochemical decomposition kinetics and activation energy of neat 1,3,5,5-tetranitrohexahydropyrimidine (DNNC) and its DNNC-d6 deuterium labeled analogue were obtained by isothermal differential scanning calorimetry (IDSC) at 142, 145, and 148 °C. Global rate constants and kinetic deuterium isotope effect (KDIE) data from the exothermic decomposition process suggest that homolytic CH bond rupture, in one or both types of chemically non-equivalent methylene (CH2) groups of the DNNC ring structure, constitutes the exothermic rate-controlling step. A DNNC-d6 energy of activation equal to 115 kJ/mol was determined for this initial autocatalytic exothermic energy release from which a 106 kJ/mol activation energy was calculated for unlabeled DNNC. This exothermic autocatalytic decomposition process follows an extended endothermic induction period for DNNC which shows a higher 128 kJ/mol activation energy during which a catalytic initiating species may form by a rate-controlling step different from CH bond rupture. 相似文献
104.
Synthesis and properties of novel poly(amide-imide)s containing pendent diphenylamino groups 总被引:1,自引:0,他引:1
A new dicarboxylic acid, 2,4-bis(N-trimellitoyl)triphenylamine, bearing two preformed imide rings was synthesized from the condensation of 2,4-diaminotriphenylamine and trimellitic anhydride at 1:2 molar ratio. A series of poly(amide-imide)s (PAIs) with inherent viscosities of 0.38-0.66 dl/g were prepared by triphenyl phosphite-activated polycondensation from the diimide-dicarboxylic acid with various aromatic diamines. All the resulting PAIs were readily soluble in a variety of organic solvents and formed strong and tough films via solution casting. These PAIs have useful levels of thermal stability associated with moderately high glass-transition temperatures (259-314 °C) and 10% weight loss temperatures in excess of 530 °C in nitrogen or in air. 相似文献
105.
Li Qiu WANG Xiao Jun PENG* Rong ZHANG Guo Quan XU Jing Nan CUI State Key Laboratory of Fine Chemicals Dalian University of Technology Dalian 《中国化学快报》2003,(1)
Indocyanine dyes as fluorescent labeling reagents have been used in bioanalysis1,2. Arylsulfonate indocyanine dyes 1d and 1e developed by Waggoner A. S. et al.3,4 have excellent fluorescent properties combined with good aqueous solubility, are a new generation of fluorescent label compounds for proteins, oligonucleotides and other compounds containing hydroxyl, mercaptol or primary amine groups5. However, photostability of these dyes has been a problem. Z. G. YAO et al.6 reported that p… 相似文献
106.
B. Kummer 《Journal of Optimization Theory and Applications》1991,70(3):561-582
The paper shows that Thibault's limit sets allow an iff-characterization of local Lipschitzian invertibility in finite dimension. We consider these sets as directional derivatives and extend the calculus in a way that can be used to clarify whether critical points are strongly stable inC
1,1 optimization problems.Many fruitful discussions with colleagues D. Klatte and K. Tammer as well as with H. Th. Jongen and F. Nozicka have influenced the present investigations in a very constructive manner. For the original papers concerning the sets f(x; u), the author is indebted to Prof. L. Thibault. 相似文献
107.
Hideki Takayasu Misako Takayasu Astero Provata Greg Huber 《Journal of statistical physics》1991,65(3-4):725-745
We study a generalized aggregation process in which charged particles diffuse and coalesce randomly on a lattice. For one-dimensional and mean-field models, we show that there exists a statistically-invariant steady state when randomly charged particles are continuously injected. The steady-state charge distribution obeys a power law with the exponent depending both on the type of the injection and on the spatial dimension. The response of the system to a perturbation (i.e., relaxation) is characterized by either a power law decay (t
–
,1) or a compressed exponential decay [exp(–t
),>1]. 相似文献
108.
A substituted polyacetylene bearing a furan ring, poly(2-propynyl 2-furoate) (PPF), was synthesized for the first time with palladium acetylide complex catalysts in CHCl3 at 60℃ to give a soluble and stable polymer with a yield of ca.75%. Some features for polymerization of 2-propynyl 2-furoate are described and discussed. The resulting polymer was characterized by IR, GPC and ^1H-NMR analysis. 相似文献
109.
Ball-like molecules with strong dipoles (labels) were mixed with synthetic polyisoprene (IR305) in low concentrations (<1%) and measured dielectrically in the frequency range 10–2–107 Hz and the temperature range –70–0°C (glass relaxation region). Calorimetric measurements showed that this type of label has a plasticizing effect on the polymeric matrix. The dielectric measurements showed that these ball-like molecules relax through cooperative rotations with the polymeric segments and at the same relaxation frequency. In addition, the label molecules showed a high-frequency local relaxation process. The relaxation strength ratio of the local process (X
local) to the total relaxation strength of the label was found to be dependent on the volume as well as on the shape of the label. A comparison between the relaxation behaviors of the ball-and rod-like molecules, having the same volume, showed that the length of the label is also an important parameter for the determination of the local contribution as well as of the cooperative relaxation mechanism of the label. The label relaxation process is discussed in relation to the molecular packing of the host polymer. 相似文献
110.
Chaoyang Wang Fang Zeng Xinxing Liu Shuizhu Wu Ping Liu 《European Polymer Journal》2005,41(1):185-191
The complexation between poly(ethylene imine) (PEI) and poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS) or AMPS copolymers was investigated with the relative excimer emission intensity IE/IM of a cationic probe 1-pyrenemethylamine hydrochloride (PyMeA · HCl), fluorescence nonradiative energy transfer (NRET) IPy/INp of naphthalene to pyrene labels, the fluorescence anisotropy r and IE/IM of pyrene labels. PEI was a hyperbranched weak polycation in acid solution, which formed complex with anionic polyelectrolytes due to the electrostatic attraction. The IE/IM of PyMeA · HCl probe decreased to zero, the intra-, intermolecular NRET IPy/INp and IE/IM of pyrene labels on the AMPS copolymers reached their maxima when χ was increased from 0 to 2.4, which was defined as the mole ratio of the amino group in PEI to the AMPS group in the polyanion. These facts indicated the formation of nonstoichiometric complex of the oppositely charged polyelectrolytes when χ = 2.4 at the concentration much lower than their overlap concentrations. The intermolecular aggregate appeared as indicated by an increase in the intermolecular IPy/INp and r with χ up to 2.4 due to neutralizing and hydrophobizing the polyelectrolytes and the bridging effect of the PEI chain bound on different polyanion chains. At high pH, PEI became a neutral polymer and did not bind with the AMPS anion to form the complex as illustrated by the constant value of r for the pyrene labels attached to the AMPS polyanion as that without addition of PEI. The amino group in PEI quenched pyrene and naphthalene emission, resulting a decrease in both INp and IPy. 相似文献