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101.
Parrondo’s Paradox has gained a fair amount of attention due to it being counter-intuitive. Given two stochastic processes, both of which are losing in nature, it is possible to have an overall net increase in capital by periodically or randomly alternating between the two processes. In this paper, we analyze the paradox with a different approach, in which we start with one process and seek to derive its complementary process. We will also state the conditions required for this to occur. Possible applications of our results include the development of future models based on the paradox. 相似文献
102.
Hui Shen Guocheng Deng Sami Kaappa Tongde Tan Ying‐Zi Han Sami Malola Shui‐Chao Lin Boon K. Teo Hannu Hkkinen Nanfeng Zheng 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(49):17895-17899
Surface organic ligands play a critical role in stabilizing atomically precise metal nanoclusters in solutions. However, it is still challenging to prepare highly robust ligated metal nanoclusters that are surface‐active for liquid‐phase catalysis without any pre‐treatment. Now, an N‐heterocyclic carbene‐stabilized Au25 nanocluster with high thermal and air stabilities is presented as a homogenous catalyst for cycloisomerization of alkynyl amines to indoles. The nanocluster, characterized as [Au25(iPr2‐bimy)10Br7]2+ (iPr2‐bimy=1,3‐diisopropylbenzimidazolin‐2‐ylidene) ( 1 ), was synthesized by direct reduction of AuSMe2Cl and iPr2‐bimyAuBr with NaBH4 in one pot. X‐ray crystallization analysis revealed that the cluster comprises two centered Au13 icosahedra sharing a vertex. Cluster 1 is highly stable and can survive in solution at 80 °C for 12 h, which is superior to Au25 nanoclusters passivated with phosphines or thiols. DFT computations reveal the origins of both electronic and thermal stability of 1 and point to the probable catalytic sites. This work provides new insights into the bonding capability of N‐heterocyclic carbene to Au in a cluster, and offers an opportunity to probe the catalytic mechanism at the atomic level. 相似文献
103.
Genlin Sun Jeong Soo Kim Yune Sung Kim Hyun Joo An Won Jo Cheong 《Journal of separation science》2019,42(16):2612-2620
A stationary phase was prepared by chemical derivatization of the support particles with a layer of copolymer composed of styrene and N‐phenyl acrylamide. Silica monolith particles of ca. 2.6 µm (volume‐based average) have been prepared as the support particles by sol‐gel reaction followed by differential sedimentation. The particles were reacted with 3‐chloropropyl trimethoxysilane followed by sodium diethyldithiocarbamate to introduce an initiator moiety. Then, the copolymer layer was immobilized via reversible addition‐fragmentation transfer polymerization. The resultant phase was packed in glass‐lined stainless‐steel micro‐columns (1 x 150 mm) and evaluated for the separation of a mixture composed of five peptides (Trp‐Gly, Thr‐Tyr‐Ser, angiotensin I, isotocin and bradykinin). The effect of monomer mixing ratio (styrene versus N‐phenyl acrylamide) on the chromatographic separation efficiency of the stationary phase was examined. A number of theoretical plates (N) as high as 33 600 plates/column (224 000 plates/m, 4.46 µm plate height) was achieved using the column packed with the optimized stationary phase. The column‐to‐column reproducibility based on three columns packed with three different batches of stationary phase was found satisfactory in separation efficiency, retention factor, and asymmetry factor. 相似文献
104.
Genlin Sun Ashraf Ali Yune Sung Kim Jeong Soo Kim Hyun Joo An Won Jo Cheong 《Journal of separation science》2019,42(24):3621-3630
A phase with both hydrophobic and hydrophilic functionalities has been synthesized by modification of ground silica monolith particles with C18 and 1‐[3‐(trimethoxysilyl)propyl] urea ligands. A series of phases was prepared by changing the ratio of the two ligands to determine the optimal ratio in view of separation efficiency. The resultant optimized stationary phase was packed in narrow‐bore glass‐lined stainless‐steel columns (1 × 300 mm and 2.1 × 100 mm) and used for the separation of synthetic peptides and proteins. The average numbers of theoretical plates (N) of 52 100/column (174 000/m, 5.75 µm plate height) and 35 500/column (118 000/m, 8.47 µm plate height) were achieved with the 300 mm column at a flow rate of 25 µL/min (0.86 mm/s) in 60:40 v/v acetonitrile/30 mM aqueous ammonium formate for the mixture of peptides (Thr‐Tyr‐Ser, Val‐Ala‐Pro‐Gly, angiotensin I, isotocin, and bradykinin) and for the mixture of proteins (myoglobin, human serum albumin, and insulin), respectively. Fast analysis of the peptides and proteins was also carried out at a flow rate of 0.9 mL/min (6.88 mm/s) with the 100 mm column and all the analytes were eluted within 2 min with good separation efficiency. 相似文献
105.
Radaelli PG Chapon LC Daoud-Aladine A Vecchini C Brown PJ Chatterji T Park S Cheong SW 《Physical review letters》2008,101(6):067205
We employ neutron spherical polarimetry to determine the nature and population of the coexisting antiferromagnetic domains in multiferroic YMn2O5. By applying an electric field, we prove that reversing the electrical polarization results in the population inversion of two types of in-plane domains, related to each other by inversion. Our results are completely consistent with the exchange-striction mechanism of ferroelectricity, and support a unified model where cycloidal ordering is induced by coupling to the main magnetic order parameter. 相似文献
106.
We report discovery of collinear-magnetism-driven ferroelectricity in the Ising chain magnet Ca3Co2-xMn(x)O6 (x approximately 0.96). Neutron diffraction shows that Co2+ and Mn4+ ions alternating along the chains exhibit an up-up-down-down ( upward arrow upward arrow downward arrow downward arrow) magnetic order. The ferroelectricity results from the inversion symmetry breaking in the upward arrow upward arrow downward arrow downward arrow spin chain with an alternating charge order. Unlike in spiral magnetoelectrics where antisymmetric exchange coupling is active, the symmetry breaking in Ca3(Co,Mn)2O6 occurs through exchange striction associated with symmetric superexchange. 相似文献
107.
Wu W Kiryukhin V Noh HJ Ko KT Park JH Ratcliff W Sharma PA Harrison N Choi YJ Horibe Y Lee S Park S Yi HT Zhang CL Cheong SW 《Physical review letters》2008,101(13):137203
We have studied quasi-two-dimensional multiferroic LuFe2O4 with strong charge-spin-lattice coupling, in which low-temperature coercivity approaches an extraordinary value of 9 T in single crystals. The enhancement of the coercivity is connected to the collective freezing of nanoscale pancakelike ferrimagnetic domains with large uniaxial magnetic anisotropy ("Ising pancakes"). Our results suggest that collective freezing in low-dimensional magnets with large uniaxial anisotropy provides an effective mechanism to achieve enhanced coercivity. This observation may help identify novel approaches for synthesis of magnets with enhanced properties. 相似文献
108.
D.G. Park D.W. Kim C.S. Angani V.P. Timofeev Y.M. Cheong 《Journal of magnetism and magnetic materials》2008
The magnetic properties of stainless steel have been investigated using a radio frequency (RF) high-temperature superconductivity (HTS) SQUID (Superconducting QUantum Interference Device)-based susceptometer. The nuclear grade 304 stainless steel is nonmagnetic at a normal condition but it changes to a partially ferromagnetic state associated with martensitic transformation under a plastic deformation. The magnetic moment of the 304 stainless steels was increased with an increasing cold work rate, and decreased with an increasing annealing temperature. The change of mechanical properties such as yield strength and ultimate tensile strength (UTS) are also analyzed in terms of deformation-induced martensitic transformation. 相似文献
109.
110.
Nonlinear Dynamics - Despite depleting the resources in their environments, some species and societies are capable of sustainable habitat expansion by alternating between a low-growth migratory... 相似文献