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91.
Dan He Seok Kyun Noh Won Seok Lyoo 《Journal of polymer science. Part A, Polymer chemistry》2011,49(21):4594-4602
Past research has examined the atom transfer radical polymerization (ATRP) with high oxidation state metal complexes and without the need for any additives such as reducing agent or free radical initiator. To extend this research, half‐metallocene ruthenium(III) (Ru(III)) catalysts were used for the polymerization of methyl methacrylate (MMA) for the first time. These catalysts were generated in situ simply by mixing phosphorus‐containing ligand and pentamethylcyclopentadienyl (Cp*) Ru(III) polymer ((Cp*RuCl2)n). The complexes in their higher oxidation state such as Cp*RuCl2(PPh3) were air‐stable, highly active, and removable catalysts for the ATRPs of MMA with both precision control of molecular weight and narrow polydispersity index. The addition of ppm amount of metal catalyst contributed to the formation of very well‐defined homopolymers and copolymers. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
92.
93.
Based on calculations using density functional theory, we show that C60 can act as a chemical Faraday cage in which a highly magnetic metal cluster with a high chemical reactivity can be encapsulated. As an example, we find that C60 can encapsulate a Fe3 cluster, while it is much less likely to encapsulate a Fe2 cluster. Spin multiplicity (=9) of the Fe3@C60 is very high, being comparable to that (=11) of a free Fe3 cluster. Geometrically, the triangular plane of the cluster is perpendicular to a S6 axis of the fullerene. 相似文献
94.
Hye Seok Park Dong Wan Seo Seung Woo Choi Young Gi Jeong Ju Ho Lee Dong Il Kim Whan‐Gi Kim 《Journal of polymer science. Part A, Polymer chemistry》2008,46(5):1792-1799
Branched sulfonated poly(ether ketone sulfone)s (Br‐SPEKS) were prepared with bisphenol A, bis(4‐fluorophenyl)sulfone, 3,3′‐disodiumsulfonyl‐4,4′‐difluorobenzophenone, and THPE (1,1,1‐tris‐p‐hydroxyphenylethane), respectively, at 180 °C using potassium carbonate in NMP (N‐methylpyrrolidinone). THPE, as a branching agent, was used with 0.4 mol % of bisphenol A to synthesize branched copolymers. Copolymers containing 10–50 mol % disulfonated units were cast from dimethylsulfoxide solutions to form films. Linear sulfonated poly(ether ketone sulfone)s (SPEKS) were also synthesized without THPE. The films were converted from the salt to acid forms with dilute hydrochloric acid. A series of copolymers were studied by Fourier transform infrared, 1H‐NMR spectroscopy, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Sorption experiments were conducted to observe the interaction of sulfonated polymers with water and methanol. The ion‐exchange capacity (IEC), a measure of proton conductivity, was evaluated. The synthesized Br‐SPEKS and SPEKS membranes exhibit conductivities (25 °C) from 1.04 × 10?3 to 4.32 × 10?3 S/cm, water swell from 20.18 to 62.35%, IEC from 0.24 to 0.83 mequiv/g, and methanol diffusion coefficients from 3.2 × 10?7 to 4.7 × 10?7 cm2/S at 25 °C. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1792–1799, 2008 相似文献
95.
Zhigang Xue Seok Kyun Noh Won Seok Lyoo 《Journal of polymer science. Part A, Polymer chemistry》2008,46(9):2922-2935
2‐[(Diphenylphosphino)methyl]pyridine (DPPMP) was successfully used as a bidentate ligand in the iron‐mediated atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) with various initiators and solvents. The effect of the catalytic system on ATRP was studied systematically. Most of the polymerizations with DPPMP ligand were well controlled with a linear increase in the number‐average molecular weights (Mn) versus conversion and relatively low molecular weight distributions (Mw/Mn = 1.10–1.3) being observed throughout the reactions, and the measured molecular weights matched the predicted values. Initially added iron(III) bromide improved the controllability of the polymerization reactions in terms of molecular weight control. The ratio of ligand to metal influenced the controllability of ATRP system, and the optimum ratio was found to be 2:1. It was shown that ATRP of MMA with FeX2/DPPMP catalytic system (X = Cl, Br) initiated by 2‐bromopropionitrile (BPN) was controlled more effectively in toluene than in polar solvents. The rate of polymerization increased with increasing the polymerization temperature and the apparent activation energy was calculated to be 56.7 KJ mol?1. In addition, reverse ATRP of MMA was able to be successfully carried out using AIBN in toluene at 80 °C. Polymerization of styrene (St) was found to be controlled well by using the PEBr/FeBr2/DPPMP system in DMF at 110 °C. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2922–2935, 2008 相似文献
96.
An efficient one-step method to prepare aryl-substituted carbazoles via tandem double or triple CC bond formations by multiple Suzuki couplings and CN bond formation by Cadogan cyclization has been developed. The developed method employs commercially available or easily preparable polybromonitrobenzenes and arylboronic acids as starting materials, tolerates various functional groups, and provides good yields. 相似文献
97.
Jin Seok Woo Chung-Hyun Cho Do Han Kim Eun Hui Lee 《Experimental & molecular medicine》2010,42(9):614-627
During membrane depolarization associated with skeletal excitation-contraction (EC) coupling, dihydropyridine receptor [DHPR, a L-type Ca2+ channel in the transverse (t)-tubule membrane] undergoes conformational changes that are transmitted to ryanodine receptor 1 [RyR1, an internal Ca2+-release channel in the sarcoplasmic reticulum (SR) membrane] causing Ca2+ release from the SR. Canonical-type transient receptor potential cation channel 3 (TRPC3), an extracellular Ca2+-entry channel in the t-tubule and plasma membrane, is required for full-gain of skeletal EC coupling. To examine additional role(s) for TRPC3 in skeletal muscle other than mediation of EC coupling, in the present study, we created a stable myoblast line with reduced TRPC3 expression and without α1SDHPR (MDG/TRPC3 KD myoblast) by knock-down of TRPC3 in α1SDHPR-null muscular dysgenic (MDG) myoblasts using retrovirus-delivered small interference RNAs in order to eliminate any DHPR-associated EC coupling-related events. Unlike wild-type or α1SDHPR-null MDG myoblasts, MDG/TRPC3 KD myoblasts exhibited dramatic changes in cellular morphology (e.g., unusual expansion of both cell volume and the plasma membrane, and multi-nuclei) and failed to differentiate into myotubes possibly due to increased Ca2+ content in the SR. These results suggest that TRPC3 plays an important role in the maintenance of skeletal muscle myoblasts and myotubes. 相似文献
98.
Past research has demonstrated that hologram of a real world object can be acquired by scanning it with a single two-dimensional optical scan. The technology commonly referred to as optical scanning holography (OSH), have found important applications such as in microscopy, pattern recognition, 3D holographic display, and optical remote sensing. As holograms are often employed to capture three dimensional objects with high resolution, large amount of data is required to represent them. In this paper we propose a method for compressing holograms based on Delta modulation. Specifically, we apply our proposed method for holograms captured by OSH. Experimental evaluation reveals that our proposed approach is capable of attaining a compression ratio of 64 times, and still preserves favorable fidelity on the reconstructed images. In addition, both the encoding and decoding processes of the proposed method are very low in complexity, hence enabling real-time operation. 相似文献
99.
A double lambda four-level system could be implemented with biexcitonic transitions on GaAs quantum well. We observed that the phase dependent biexcitonic transition could be explained by interference between one-photon and three-photon transition in a double lambda four-level system. An ultralow-light switch pulse could control 80% of biexcitonic absorption, which demonstrated all-optical switching with biexcitonic double lambda system. 相似文献
100.
Min Hwan Lee Kyung Min Kim Seul Ji Song Sang Ho Rha Jun Yeong Seok Ji Sim Jung Gun Hwan Kim Jung Ho Yoon Cheol Seong Hwang 《Applied Physics A: Materials Science & Processing》2011,102(4):827-834
The bipolar resistive switching mechanisms of a p-type NiO film and n-type TiO2 film were examined using local probe-based measurements. Scanning probe-based current–voltage (I–V) sweeps and surface potential/current maps obtained after the application of dc bias suggested that resistive switching is
caused mainly by the surface redox reactions involving oxygen ions at the tip/oxide interface. This explanation can be applied
generally to both p-type and n-type conducting resistive switching films. The contribution of oxygen migration to resistive
switching was also observed indirectly, but only in the cases where the tip was in (quasi-) Ohmic contact with the oxide. 相似文献