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41.
A series of titanium complexes [(Ar)NC(CF3)CHC(R)O]2TiCl2 (4b: Ar = -C6H4OMe(p), R = Ph; 4c: Ar = -C6H4Me(p), R = Ph; 4d: Ar = -C6H4Me(o), R = Ph; 4e: Ar = α-Naphthyl, R = Ph; 4f: Ar = -C6H5, R = t-Bu; 4g: Ar = -C6H4OMe(p); R = t-Bu; 4h: Ar = -C6H4Me(p); R = t-Bu; 4i: Ar = -C6H4Me(o); R = t-Bu) has been synthesized and characterized. X-ray crystal structures reveal that complexes 4b, 4c and 4h adopt distorted octahedral geometry around the titanium center. With modified methylaluminoxane (MMAO) as a cocatalyst, complexes 4b-c and 4f-i are active catalysts for ethylene polymerization and ethylene/norbornene copolymerization, and produce high molecular weight polyethylenes and ethylene/norbornene alternating copolymers. In addition, the complex 4c/MMAO catalyst system exhibits the characteristics of a quasi-living copolymerization of ethylene and norbornene with narrow molecular weight distribution. 相似文献
42.
P.S. Vijayanand 《European Polymer Journal》2007,43(5):2046-2056
The novel methacrylic monomer, 4-nitro-3-methylphenyl methacrylate (NMPM) was synthesized by reacting 4-nitro-3-methylphenol dissolved in ethyl methyl ketone (EMK) with methacryloyl chloride in the presence of triethylamine as a catalyst. The homopolymer and copolymers of NMPM with glycidyl methacrylate having different compositions were synthesized by free radical polymerization in EMK solution at 70 ± 1 °C using benzoyl peroxide as free radical initiator. The homopolymer and the copolymers were characterized by FT-IR, 1H NMR and 13C NMR spectroscopic techniques. The solubility tests were tested in various polar and non-polar solvents. The molecular weight and polydispersity indices of the copolymers were determined using gel permeation chromatography. The glass transition temperature of the copolymers increases with increase in NMPM content. The thermogravimetric analysis of the polymers performed in air showed that the thermal stability of the copolymer increases with NMPM content. The copolymer composition was determined using 1H NMR spectra. The monomer reactivity ratios were determined by the application of conventional linearization methods such Fineman-Ross (r1 = 1.862, r2 = 0.881), Kelen-Tudos (r1 = 1.712, r2 = 0.893) and extended Kelen-Tudos methods (r1 = 1.889, r2 = 0.884). 相似文献
43.
《Electroanalysis》2006,18(11):1097-1104
Copolymerization of an osmium(II) functionalized pyrrole moiety, osmium‐bis‐N,N'‐(2,2′‐bipyridyl)‐N‐(pyridine‐4‐ylmethyl‐(8‐pyrrole‐1yl–octyl)‐amine)chloride ( I ) with 3‐methylthiophene was carried out. The resulting conducting polymer film exhibited a clear redox couple associated with the Os3+/2+ response and the familiar conducting polymer backbone signature. The effect of film thickness upon the redox properties of the copolymer was investigated in organic electrolyte solutions. Scanning electron micrographs (SEM) along with energy dispersive X‐ray (EDX) spectra of the copolymerized films were undertaken, both after formation and redox cycling in neutral buffer solution. These clearly show that electrolyte is incorporated into the polymer film upon redox cycling through the Os3+/2+ redox system. The Os3+/2+ response associated with the copolymer was seen to be significantly altered in the presence of ascorbic acid both in acidic and neutral pH buffer solutions. This pointed to an electrocatalytic reaction between the ascorbic acid and the Os3+ form of the copolymer. Under acidic conditions the copolymer film exhibited a sensitivity of 1.76 (±0.05) μA/mM with a limit of detection (LOD) of 1.45 μM for ascorbic acid. Under neutral pH conditions the copolymer exhibited a sensitivity of 19.26 (±1.05) μA/mM with a limit of detection (LOD) of 1.28 μM for ascorbic acid. 相似文献
44.
Lyotropic liquid crystalline poly(aryl ether ketone) copolymer containing phthalazinone moiety and biphenyl mesogen 总被引:1,自引:0,他引:1
Qingmin Sun 《European Polymer Journal》2007,43(8):3683-3687
A novel lyotropic liquid crystalline material poly(aryl ether ketone) copolymer containing phthalazinone moiety and biphenyl mesogen named P-8515 was developed by a mild solution polycondensation method. The molecular weight (Mn) was 53,000 and the value of molecular weight distribution index (MDI) was 2.49 detected by GPC. The critical concentration (C∗) of P-8515 was 36 wt% and P-8515 exhibited characteristic nematic lyotropic liquid crystalline phases in NMP solution at different concentrations and the phase morphology changed to a typical threaded texture when shear forces were induced from PLM observations. The Tg value was 238 °C and the value for 5% weight loss temperature was 515 °C in nitrogen from DSC and TGA determinations, respectively. 相似文献
45.
Investigations on a new class of polyamides obtained by interfacial polycondensation from amine-chloral derivatives, e.g., 2,2-bis(p-aminophenyl)-1,1,1-trichloromethane or 2,2-bis(p-aminophenyl)-1, 1-dichloroethylene and terephthaloyl chloride, have been carried out. It was found that the interfacial process proceeds in the most advantageous way in acidic medium at 0°C using equivalent volume amounts and equimolar concentrations of methylene chloride and water phases in the presence of a stoichiometric quantity of triethylamine as the hydrogen acceptor. 相似文献
46.
Polymer-bound alkylthiopurine and -pyrimidine bases were prepared and used as the polymeric reagents for the reactions of nitrile, olefin, and enone formation. The corresponding low molecular weight compounds were also prepared for comparison. Differences in the reactivity of these reagents were related to the change in tautomerism of the purine and pyrimidine moieties. 相似文献
47.
Maria Pizzoli Giovanni Pezzin Giuseppina Ceccorulli 《Journal of Macromolecular Science: Physics》2013,52(2):241-250
Samples of poly(vinyl chloride) plasticized with variable amounts of either dibutyl phthalate (DPB) or dicyclohexyl phthalate (DCHP) were investigated by dynamic-mechanical measurements in the β relaxation temperature range. In this range of temperature, a superposition of the relaxation due to the cyclohexyl group with the PVC β peak was found for the samples plasticized with DCHP. By studying the dependence of the activation energy and of the peak broadness on the DCHP concentration it was possible to show that the PVC β relaxation is reduced to zero at the critical plasticizer weight fraction W1 = 0.2. For the PVC-DBP series the β peak disappears at the same plasticizer content. These results strengthen the hypothesis that the β peak of PVC is due to a kind of cooperative motion since 1 mole of plasticizer for every 20 repeating units of the polymer is sufficient to suppress the PVC β relaxation. 相似文献
48.
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50.
The free-radical initiated copolymerization of 2-(4-chloro-1-naphtyloxy)-2-oxoethyl methacrylate (ClNOEMA) with 2-(diethylamino) ethyl methacrylate (DEAEMA) was carried out in 1,4-dioxane solution at 70 ± 1°C using 2,2′-azobisisobutyronitrile (AIBN) as an initiator with different monomer-to-monomer ratios (ranging from 0.15 to 0.85) in the feed. The copolymer composition obtained by elemental analysis led to the determination of reactivity ratios employing Fineman-Ross (F-R) and Kelen-Tüdös (KT) linearization methods. These parameters were also estimated using a non-linear computational fitting procedure, known as reactivity ratios error in variable model (RREVM). The prepared homo and copolymers were tested for their antimicrobial activity against bacteria and yeast. These copolymers have been converted into novel salts by reaction with the iodemethane (CH3I). The copolymers and the corresponding salts have been characterized fully by a range of spectroscopic analysis techniques. The electrical conductivity dependence of temperature of the polymers were measured and the polymers exhibit the semi-conducting behavior, confirming that the electrical conductivity increases with increasing temperature. The poly(CINOEMA-co-DEAEMA) polymer doped by CH3I for 15 min shows the highest conductivity. The optical band gap, activation energy and room temperature conductivity values of these polymers were obtained. These electronic parameters suggest that the poly(CINOEMA-co-DEAEMA)s doped by CH3I for 15 min is an organic semiconductor with the thermally activated conduction mechanism. 相似文献