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891.
Zhi‐En Lin Wei Fan Naotaka Chino Feifei Gao Toshiyuki Yokoi Tatsuya Okubo 《无机化学与普通化学杂志》2006,632(3):465-468
A new organically templated nickel–zinc phosphate, [C2N2H10]·[Ni2.4Zn3.6(PO4)4(HPO4)]·H2O, has been synthesized from an aqueous solution containing NiCl2·6H2O, Zn(OAc)2·2H2O, H3PO4 and ethylenediamine as the structure‐directing agent. The compound crystallizes in the monoclinic system, space group C2/c (No. 15), a = 19.1563(5), b = 5.0316(2), c = 21.1724(5) Å, α = 103.201(3)°, V = 1986.81(11) Å3, Z = 4. It possesses a three‐dimensional framework constructed from MO4 (M = Ni, Zn), PO4, and HPO4 tetrahedra through their vertices. One‐dimensional 8‐ring channels are found in the structure, with the diprotonated organic templates residing in the tunnels and interacting with the inorganic framework by extensive hydrogen bonds. The framework is characterized by infinite helical chains of corner‐sharing MO4 (M = Ni, Zn) tetrahedra. 相似文献
892.
Naohiro Hanyu Mamoru Hatakeyama Toshiyuki Tanaka Masaru Tada Adarsh Sandhu Masanori Abe Hiroshi Handa 《Journal of magnetism and magnetic materials》2009,321(10):1625-1627
For affinity purification of drug target protein we have developed magnetic carriers, narrow in size distribution (184±9 nm), which exhibit minimal non-specific binding of unwanted proteins. The carriers were highly dispersed in aqueous solutions and highly resistant to organic solvents, which enabled immobilization of various hydrophobic chemicals as probes on the carrier surfaces. Utilizing the carriers we have automated the process of separation and purification of the target proteins that had been done by manual operation previously. 相似文献
893.
894.
Visible actions on symmetric spaces 总被引:1,自引:0,他引:1
Toshiyuki Kobayashi 《Transformation Groups》2007,12(4):671-694
A visible action on a complex manifold is a holomorphic action that admits a J-transversal totally real submanifold S. It
is said to be strongly visible if there exists an orbit-preserving anti-holomorphic diffeomorphism σ such that σ|S = id. In this paper we prove that for any Hermitian
symmetric space D = G/K the action of any symmetric subgroup H is strongly visible. The proof is carried out by finding explicitly
an orbit-preserving anti-holomorphic involution and a totally real submanifold S. Our geometric results provide a uniform
proof of various multiplicity-free theorems of irreducible highest weight modules when
restricted to reductive symmetric pairs, for both classical and exceptional cases, for both finite- and infinite-dimensional
cases, and for both discrete and continuous spectra. 相似文献
895.
896.
There is very limited knowledge of the kinematical relations for the velocity structure functions higher than three. Instead, the dynamical equations for the structure functions of the velocity increment are obtained from the Navier–Stokes equation under the assumption of the local homogeneity and isotropy. These equations contain the correlation between the velocity and pressure gradient increments, which is very difficult to know theoretically and experimentally. We have examined these dynamical relations by using direct numerical simulation data at very high resolution at large Reynolds numbers, and found that the contribution of the pressure term is important to the dynamics of the longitudinal velocity with large amplitudes. The pressure term is examined from the view point of the conditional average and the role of the pressure term in the turbulence dynamics is discussed. 相似文献
897.
Shinsuke Ifuku Yoshinobu Tsujii Hiroshi Kamitakahara Toshiyuki Takano Fumiaki Nakatsubo 《Journal of polymer science. Part A, Polymer chemistry》2005,43(21):5023-5031
The 3‐ferrocenoylpropanoyl group, one of the redox species, was introduced at C‐2 and/or C‐3 positions of 6‐O‐(4‐stearyloxytrityl)cellulose. The spreading behavior of the cellulose derivatives on the water surface and the properties of Langmuir–Blodgett (LB) films were investigated. The surface pressure–area isotherm of the cellulose monolayer was changed by the subphase temperature. Uniform monolayers of 6‐O‐(4‐stearyloxytrityl)cellulose 3‐ferrocene propionate (STCFc) could be deposited successively onto several substrates by the horizontal lifting method at 10 mN m?1, and this produced X‐type LB films. The successive uniform depositions of STCFc were confirmed by ultraviolet–visible absorption spectra. X‐ray diffraction measurements indicated that the thickness of the STCFc molecules in the LB films was 1.99 nm. Fourier transform infrared spectroscopy measurements supported the idea that hydrocarbon chains in the LB films were highly ordered (trans‐zigzag) and oriented considerably perpendicular to the surface of the substrate. Moreover, the C?O group of the ferrocenoyl groups was perpendicular to the surface of the substrate, and the ferrocene group was occupied in the water phase. Cyclic voltammograms for the STCFc monolayer on a gold electrode exhibited surface waves. The interfacial electron‐transfer process between the redox site incorporated into the cellulose LB monolayer and the electrode surface was fast enough at a scanning rate lower than 100 mV s?1. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5023–5031, 2005 相似文献
898.
899.
In this study, we assessed the boron adsorption characteristic of our synthesized adsorbent: polyallylamine-beads-glucose (PAA-Glu) by using the adsorption amount and adsorption site availability (ASA), and determined the optimum conditions for PAA-Glu synthesis. ASA is our proposed indicator and it expresses the percentage of the experimental equilibrium adsorption in relation to the theoretical equilibrium adsorption and indicates the availability of adsorption sites (hydroxyl groups) on adsorbents. We investigated the effects of the degree of cross-linking (20, 40 and 60 %), the introduction amount of α-D-glucose (40, 60 and 80 %), and the introduction temperature (30–150 °C) as regards PAA-Glu on the boron adsorption amount. The boron adsorption amount for PAA-Glu (20 % cross-linked, 30 °C) was superior to that for another degree of cross-linked PAA-Glu. However, the ASA for PAA-Glu (60 % cross-linked, 30 °C) exhibited the best value in this synthesized PAA-Glu. Furthermore, we examined the introduction temperature at which glucose was introduced to PAA-Glu (20 % cross-linked) in the 30–150 °C range, and we confirmed that the optimum temperature range for the synthesis of PAA-Glu was 60–80 °C. We found that controlling the space between the main chains of the polymer by using a spacer such as a cross-linker allowed boron molecules to come and go and led to an improvement in the boron adsorption amount and ASA. 相似文献
900.
Toshiyuki Kataoka Tomoyuki Ohishi Tsutomu Yokozawa Takayuki Ikehara 《Journal of Polymer Science.Polymer Physics》2010,48(15):1732-1739
The solution, gelation, and morphological properties of monodisperse aromatic polyamide diblock copolymers consisting of poly(p‐benzamide) (PpBA), poly(m‐benzamide) (PmBA), and poly(N‐octyl m‐benzamide) (POmBA) were investigated. The block copolymers of these polymers, PpBA‐block‐POmBA and PmBA‐block‐POmBA, formed spherical micelles or amorphous aggregates in many solvents in addition to physical gels at concentrations higher than 5 wt %. A temperature‐induced sol‐gel transition was also exhibited for PpBA‐block‐POmBA in solvents with high boiling points such as N,N‐dimethylacetamide and N‐methylpyrrolidone (NMP), although the transition was not entirely thermoreversible; the transition temperature decreased by annealing at ~80 °C. Dynamic light scattering measurements of the PpBA‐block‐POmBA/NMP solutions revealed that metastable micelles in the sol state reorganized into smaller micelles upon annealing at 90 °C. The block copolymer, which forms strong associations, exhibited some transient structure as indicated by the need to sufficiently anneal the solution to reach equilibrium. Network‐like patterns with characteristic length of ~10 μm appeared on the gel surfaces upon evaporation of volatile solvents such as dichloromethane and chloroform, in which the copolymers were observed to aggregate. The unique properties of the copolymers originate from interactions between the highly polar N? H aromatic polyamide blocks. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1732–1739, 2010 相似文献