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991.
钙作为合金元素对铝在碱溶液中的缓蚀作用及其与酒石酸盐的协同效应 总被引:1,自引:0,他引:1
通过集气法、极化曲线和电化学阻抗谱研究了在铝中添加合金元素钙对其在碱 溶液中的缓蚀作用及其与酒石酸盐的协同效应。实验结果表明,铝电极的腐蚀速率 随钙含量的增加而减小。溶液中不含酒石酸盐时,钙对电极反应的阴极过程有显著 的抑制作用,对阳极过程作用不明显;而当溶液中含有酒石酸盐时,阴极过程和阳 极过程均被显著抑制。阻抗谱的解析结果还表明,钙离子或酒石酸钙络离子是通过 减小反应物在活性位上的反应速率而起缓蚀作用的,它们可能属于界面型缓蚀剂而 非成相型缓蚀剂。 相似文献
992.
Summary The muramyldipeptide derivative B30-MDP has immunoadjuvant activity and vesicleforming ability in aqueous solutions. To assist in the clinical application of B30-MDP to liposomal vaccine, we investigated the physicochemical properties including membrane fluidity, surface charge and particle size of B30-MDP vesicles containing cholesterol, dipalmitoylphosphatidyl-choline (DPPC) or dipalmitoylphosphatidylglycerol (DPPG).The membrane fluidity of B30-MDP/cholesterol vesicles was slightly influenced by cholesterol concentration and temperature. The membrane fluidity of B30-MDP/phospholipid vesicle was dependent on temperature. ESR spectra clearly showed the good miscibility of cholesterol with B30-MDP and the occurrence of phase separation between B30-MDP and phospholipid.The surface charge and particle size of B30-MDP/cholesterol vesicles were hardly influenced by cholesterol concentration in the membrane because the membrane surface was covered with the hydrophilic region of B30-MDP. The effect of this hydrophilic region of B30-MDP on the surface charge and particle size of B30-MDP/phospholipid vesicle was greater than that of phospholipid.This study showed that the membrane structure of B30-MDP/cholesterol vesicle differed from that of B30-MDP/phospholipid vesicle. Further, the hydrophilic region of B30-MDP is considered to play an important role in the physicochemical properties and formation of the vesicle. 相似文献
993.
The title compound (C17H16O2, Mr = 252.30) crystallizes in the monoclinic system,
space group P21/c with a = 11.5763(14), b = 11.0321(11), c = 11.5094(13) (A),β = 114.581(3)°, V=
1336.7(3) (A)3, Z = 4, Dc = 1.254 g/cm3, μ(MoKa) = 0.081 cm-1 and F(000) = 536.00. The final R
and wR are 0.0527 and 0.1285, respectively for 3058 observed reflections (I > 2σ(I)). In the title
molecule, two phenyl rings are rotated oppositely with respect to the central part C(1)-C(2)=C(3)-
C(4) (plane 3) and the dihedral angle between them is 14.8°. The phenone O(1) atom deviates from
plane 3 by 0.291(A). In the crystal the molecules form H-bond chains of R21(6) and R21 (5) types
similar crystals are also presented. 相似文献
994.
995.
The vesicle structures of egg yolks phosphatidylcholine/didodecyldimethylammonium bromide (1 : 1, mass ratio) deposited on mica were studied by atomic force microscopy (AFM) both in aqueous phase and air. In aqueous phase both bilayer and domelike vesicles with a mean diameter of 45 nm were observed, whereas in air the structure was more complicated depending on the initial concentration of vesicles. Vesicles with the original size could only be visualized at very low concentration with a mean diameter of 55 nm, which is a little larger than the result obtained in aqueous phase. At higher concentrations, fused large aggregates and multiple bilayer with a thickness ca. 4 nm of each bilayer were dominated. A plausible adsorption mechanism was proposed based on the experimental results. 相似文献
996.
Dependence of surface-enhanced Raman scattering (SERS) from Calf thymus DNA on anions is investigated.With the silver colloid,the bands at 732,960 and 1333 cm-1 for adenine (A),1466 cm-1 for deoxyribose,and 1652 cm-1 for the C=O group of thymine (T) are observably enhanced.With the presence of the Cl- or SO42- anions,the bands at 732 and 1326/1329 cm-1 for the symmetric stretching and skeletal vibrational modes of adenine (A) are dramatically enhanced,and the enhancement effect with the SO24- ion is more than that with the Cl- ion.The experimental results show that the DNA molecule can be adsorbed on the silver colloid particles through the C6N and N7 of adenine (A),the C=O of thymine (T) and deoxyribose.Moreover,the formed hydrogen bonding of the Cl- or S2O4- ions to the C6NH2 group of adenine (A) can induce larger C6N electronegativity,which is favor for the C6N/N7 cooperative adsorption on the (Ag) n colloid particles. 相似文献
997.
Harry W. Gibson Aurica Farcas Jason W. Jones Zhongxin Ge Feihe Huang Matthew Vergne David M. Hercules 《Journal of polymer science. Part A, Polymer chemistry》2009,47(14):3518-3543
Dibenzo‐24‐crown‐8‐terminated polystyrene ( 5 ) was chain extended to “dimeric” 8 by pseudorotaxane formation with a ditopic guest, α,ω‐bis[p‐(N‐benzylammoniomethyl)phenoxy]heptane bis(hexafluorophosphate) ( 7 ). The three‐armed star polymer 11 was similarly formed by complexation of the dibenzo‐24‐crown‐8‐terminated polystyrene ( 5 ) with a tritopic secondary ammonium salt, 1,3,5‐tris[p‐(benzylammoniomethyl)phenyl]benzene tris(hexafluorophosphate) ( 10 ). Another three‐armed star polymer 13 was self‐assembled from dibenzo‐24‐crown‐8‐terminated polystyrene ( 5 ) and a tetratopic paraquat compound, 1,2,4,5‐tetrakis{p‐N‐[(N′‐methyl‐4,4′‐bipyridinium)methylphenyl]}benzene octakis(hexafluorophosphate) ( 12 ). The above chain extension and star polymer formation processes seemed to be cooperative; that is, the second and third complexation steps proceed with stepwise higher efficiencies than statistically expected. Dibenzo‐24‐crown‐8‐terminated polystyrene ( 5 ) was chain extended with secondary ammonium terminated polystyrene 14 , forming 16 , and also self‐assembled with a secondary ammonium ion terminated polyisoprene 15 to form supramolecular block copolymer 17 . These processes were examined by NMR, mass spectrometry and viscometery. Thus, although binding in these systems is not particularly strong (association constants <104 M?1), these examples provide proof‐of‐principle that pseudorotaxane formation is a viable concept for chain extension and self‐assembly of novel types of block copolymers and star polymers. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3518–3543, 2009 相似文献
998.
999.
Aleksey D. Drozdov 《Journal of Polymer Science.Polymer Physics》2001,39(12):1312-1325
Governing equations are derived for the kinetics of physical aging in polymeric glasses. An amorphous polymer is treated as an ensemble of cooperatively rearranged regions (CRRs). Any CRR is thought of as a string of elementary clusters (ECs). Fragmentation of the string occurs at random times at any border between ECs. Two strings aggregate at random instants to produce a new string. Aggregation and fragmentation are treated as thermally activated processes, and the rate of fragmentation is assumed to grow with temperature more rapidly than the rate of coalescence. A nonlinear differential equation is developed for the distribution of CRRs with various numbers of ECs. Adjustable parameters of the model are found by the fitting of experimental data for polycarbonate, poly(methyl methacrylate), polystyrene, and poly(vinyl acetate) (PVA). Fair agreement is established between observations and results of numerical simulation. For PVAc, the relaxation spectrum found by matching data in a calorimetric test is successfully employed to predict experimental data in a shear relaxation test. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1312–1325, 2001 相似文献
1000.
Inferior players in simple games 总被引:2,自引:0,他引:2
Power indices like those of Shapley and Shubik (1954) or Banzhaf (1965) measure the distribution of power in simple games.
This paper points at a deficiency shared by all established indices: players who are inferior in the sense of having to accept
(almost) no share of the spoils in return for being part of a winning coalition are assigned substantial amounts of power.
A strengthened version of the dummy axiom based on a formalized notion of inferior players is a possible remedy. The axiom
is illustrated first in a deterministic and then a probabilistic setting. With three axioms from the Banzhaf index, it uniquely
characterizes the Strict Power Index (SPI). The SPI is shown to be a special instance of a more general family of power indices
based on the inferior player axiom.
Received: December 1999/Final version: June 2001 相似文献