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981.
离散坐标法在计算生物组织内光场空间角分布中的应用 总被引:5,自引:5,他引:0
从辐射传输理论出发,研究了准直光照下层状生物组织内漫射光场的角分布.在辐射传输方程的基础上,采用离散坐标法得到了描述层状生物组织内漫射光传输问题的微分方程组形式,并用特征值-特征矢量方法对其进行了求解,给出了通解形式.结合边界条件对两类典型生物组织内漫射光场角分布进行了数值计算-各向同性组织和前向散射组织,给出了组织内不同深度处漫射光场空间角分布曲线.通过对计算结果比较分析,得到了生物组织内漫射光场空间角分布随深度的变化规律,及边界效应和光学参量对组织内漫射光场空间角分布的影响. 相似文献
982.
Nagaoka S Fukuzawa H Prümper G Takemoto M Takahashi O Yamaguchi K Kakiuchi T Tabayashi K Suzuki IH Harries JR Tamenori Y Ueda K 《The journal of physical chemistry. A》2011,115(32):8822-8831
In an aim to create a "sharp" molecular knife, we have studied site-specific fragmentation caused by Si:2p core photoionization of bridged trihalosilyltrimethylsilyl molecules in the vapor phase. Highly site-specific bond dissociation has been found to occur around the core-ionized Si site in some of the molecules studied. The site specificity in fragmentation and the 2p binding energy difference between the two Si sites depend in similar ways on the intersite bridge and the electronegativities of the included halogen atoms. The present experimental and computational results show that for efficient "cutting" the following conditions for the two atomic sites to be separated by the knife should be satisfied. First, the sites should be located far from each other and connected by a chain of saturated bonds so that intersite electron migration can be reduced. Second, the chemical environments of the atomic sites should be as different as possible. 相似文献
983.
Zurawski A Mai M Baumann D Feldmann C Müller-Buschbaum K 《Chemical communications (Cambridge, England)》2011,47(1):496-498
Homoleptic frameworks of the formula [Sr(1-x)Eu(x)(Im)(2)] (1) (x = 0.01-1.0; Im(-) = imidazolate anion, C(3)H(3)N(2)(-)) are hybrid materials that exhibit an intensive green luminescence. Tuning of both emission wavelength and quantum yield is achieved by europium/strontium substitution so that a QE of 80% is reached at a Eu content of 5%. Even 100% pure europium imidazolate still shows 60% absolute quantum efficiency. Substitution of Sr/Eu shows that doping with metal cations can also be utilized for coordination compounds to optimize materials properties. The emission is finely tuneable in the region 495-508 nm via variation of the europium content. The series of frameworks [Sr(1-x)Eu(x)(Im)(2)] presents dense MOFs with the highest quantum yields reported for MOFs so far. 相似文献
984.
Rotili D Altun M Hamed RB Loenarz C Thalhammer A Hopkinson RJ Tian YM Ratcliffe PJ Mai A Kessler BM Schofield CJ 《Chemical communications (Cambridge, England)》2011,47(5):1488-1490
Photoactivated cross-linking of peptides to proteins is a useful strategy for identifying enzyme-substrate and protein-protein interactions in cell lysates as demonstrated by studies on the human hypoxia inducible factor system. 相似文献
985.
Fang S Fueangfung S Lin X Zhang X Mai W Bi L Green SA 《Chemical communications (Cambridge, England)》2011,47(4):1345-1347
Synthetic oligodeoxynucleotide is purified by capping failure sequences with an acrylated phosphoramidite followed by polymerization and product extraction. The method is suitable for large scale oligonucleotide drug purification. 相似文献
986.
Chunguang Wang Zishou Zhang Kancheng Mai 《Journal of Thermal Analysis and Calorimetry》2011,106(3):895-903
β-nucleated PP/PET blends were prepared using nano-CaCO3 supported β-nucleating agent (β-NA), PP as matrix, and PET as dispersion phase. The effects of preparation methods, PET content, and melting temperature
on the non-isothermal crystallization behavior and the melting characteristic and polymorphic composition of PP in the blends
were investigated by differential scanning calorimeter (DSC) and wide angle X-ray diffraction (WAXD). The results indicated
that the PP crystallized predominantly in β-modification in the presence of β-NA. However, efficiency of β-NA for PP crystallization decreased with addition of PET and increasing PET contents. The β-nucleation of β-NA for PP crystallization in the blends was dependant on the preparation methods. The high β-nucleation and high β-PP content were obtained for PP/PET blend prepared at the temperature of 265 °C and added the β-NA into the blend at the temperature of 180 °C. However, the addition of β-PP or β-NA into blends at 265 °C decreased the β-nucleation, and no β-PP was formed because the β-NA mainly dispersed on the PET dispersion phase or at the interface between PP and PET. 相似文献
987.
Tyrosinase inhibitory activity-guided fractionation of the bark of Peltophorum dasyrachis (yellow batai) led to the isolation of the six active compounds which were characterised as six flavonoids: apigenin (1), (+)-2,3-trans-dihydrokaempferol (2), (+)-2,3-trans-dihydrokaempferol-3-O-α-L-rhamnoside (3), (+)-4',7-dimethoxy-2,3-trans-dihydroquercetin (4), (+)-2,3-trans-dihydroquercetin (5) and (-)-2,3-trans-dihydroquercetin-3-O-α-L-rhamnoside (6). All compounds were isolated for the first time from the bark of P. dasyrachis. Moreover, all compounds were evaluated for tyrosinase activities towards L-DOPA as the substrate. We observed that compounds 2 and 5 showed potent inhibitory effects (IC?? values were 126?±?3.2 and 210?±?5.8?μM, respectively). In general, for flavonoids the 3',4'-dihydroxy group's substituent is a more potent inhibitor than the 4'-hydroxy group substituent, i.e. quercetin?>?kaempferol. Interestingly, our result in the oxidation of L-DOPA showed that the 4'-hydroxy group substituent (compound 2) is a more potent inhibitor than the 3',4'-dihydroxy group substituent (compound 5). This result showed a new relationship between tyrosinase inhibitory activities and flavonoids. The kinetic analyses by Lineweaver-Burk plots showed that both the compounds 2 and 5 behaved as competitive inhibitors of L-DOPA oxidation. 相似文献
988.
In situ oxidation study of Pt(110) and its interaction with CO 总被引:1,自引:0,他引:1
Butcher DR Grass ME Zeng Z Aksoy F Bluhm H Li WX Mun BS Somorjai GA Liu Z 《Journal of the American Chemical Society》2011,133(50):20319-20325
Many interesting structures have been observed for O(2)-exposed Pt(110). These structures, along with their stability and reactivity toward CO, provide insights into catalytic processes on open Pt surfaces, which have similarities to Pt nanoparticle catalysts. In this study, we present results from ambient-pressure X-ray photoelectron spectroscopy, high-pressure scanning tunneling microscopy, and density functional theory calculations. At low oxygen pressure, only chemisorbed oxygen is observed on the Pt(110) surface. At higher pressure (0.5 Torr of O(2)), nanometer-sized islands of multilayered α-PtO(2)-like surface oxide form along with chemisorbed oxygen. Both chemisorbed oxygen and the surface oxide are removed in the presence of CO, and the rate of disappearance of the surface oxide is close to that of the chemisorbed oxygen at 270 K. The spectroscopic features of the surface oxide are similar to the oxide observed on Pt nanoparticles of a similar size, which provides us an extra incentive to revisit some single-crystal model catalyst surfaces under elevated pressure using in situ tools. 相似文献
989.
Araoz R Servent D Molgó J Iorga BI Fruchart-Gaillard C Benoit E Gu Z Stivala C Zakarian A 《Journal of the American Chemical Society》2011,133(27):10499-10511
Pinnatoxins belong to an emerging class of potent marine toxins of the cyclic imine group. Detailed studies of their biological effects have been impeded by unavailability of the complex natural product from natural sources. This work describes the development of a robust, scalable synthetic sequence relying on a convergent strategy that delivered a sufficient amount of the toxin for detailed biological studies and its commercialization for use by other research groups and regulatory agencies. A central transformation in the synthesis is the highly diastereoselective Ireland-Claisen rearrangement of a complex α,α-disubstituted allylic ester based on a unique mode for stereoselective enolization through a chirality match between the substrate and the lithium amide base. With synthetic pinnatoxin A, a detailed study has been performed that provides conclusive evidence for its mode of action as a potent inhibitor of nicotinic acetylcholine receptors selective for the human neuronal α7 subtype. The comprehensive electrophysiological, biochemical, and computational studies support the view that the spiroimine subunit of pinnatoxins is critical for blocking nicotinic acetylcholine receptor subtypes, as evidenced by analyzing the effect of a synthetic analogue of pinnatoxin A containing an open form of the imine ring. Our studies have paved the way for the production of certified standards to be used for mass-spectrometric determination of these toxins in marine matrices and for the development of tests to detect these toxins in contaminated shellfish. 相似文献
990.
ZCVI?-2 is a newly developed furoxan-based nitric oxide-releasing derivative of oleanolic acid. It exhibited strong cytotoxicity against human hepatocellular carcinoma (HCC) in vitro and significantly inhibited the growth of HCC tumors in vivo. However, its low aqueous solubility and toxicity due to the fast release of nitric oxide (NO) in blood challenged its formulation. In the present investigation, the interaction characteristics of ZCVI?-2 with bovine serum albumin (BSA) were studied by fluorescence spectrometry, synchronous fluorescence spectra and Fourier transform-infrared (FT-IR). It was found that ZCVI?-2 concentration, temperature and pH had significant effect on the interactions. ZCVI?-2 was able to bind BSA with high affinity, low temperature and neutral pH favor the binding. The interaction exhibited to be a spontaneous and exothermic process. ZCVI?-2 was buried in the hydrophobic pocket in subdomain IIB of BSA and the exact binding site was around 3.83 nm in average from Trp212. The NO releasing characteristics of nanocomplexes were compared with ZCVI?-2 solution by Griess Reagent Method. It was found that the release of NO from ZCVI?-2/BSA nanocomplexes was retarded significantly, thus making ZCVI?-2 into a BSA-bound nanocomplexes had the great potential to lower the toxicity due to the absence of organic solvents and surfactants and meanwhile the sustained release of NO. 相似文献