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1.
Fixed-frequency and threshold photoelectron spectra have been recorded for ionization from the S ls shells in SF6, CS2 and COS, the Si 1s shells in SiH4 and SiCl4 and the Cl 1s shell in SiCl4 using synchrotron radiation. Fixed-frequency spectra generally showed a single strong ionization feature with associated weak satellite structure due to excited ionized states. Threshold spectra closely resembled X-ray absorption spectra but with an additional feature due to direct ionization. In cases where resonant process enhanced the NEXAFS spectrum direct ionization was not observed. 相似文献
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Y. Zhang T. M. Benson P. Sewell A. Vukovic D. Zhang W. J. Pan A Loni D. Furniss A. B. Seddon 《Optical and Quantum Electronics》2006,38(1-3):97-110
This paper presents our recent simulation results and novel designs of single mode large cross-section glass-based waveguides for photonic integrated circuits (PICs). Simulations were performed using an in-house Finite Difference (FD) based mode solver and the FD Beam propagation Method (FD-BPM). Our simulation results show that this innovative technology could provide a simplified means to couple optical energy efficiently between optical components in a single chip. This would provide the base for the future large-scale integration of optical components in PICs. The novel idea of using single mode large cross-section glass-based waveguides as an optical integration platform is an evolutionary innovative solution for the monolithic integration of optical components, in which the glass-based structures act both as waveguides and as an optical bench for integration. This allows easy and efficient optical coupling between optical components and optical fibres, removing costly and tedious alignment problems and considerably reducing optical coupling losses in PICs. We expect that the glass-based waveguide PICs technology will enable the emergence of a new generation of compact, reliable, high speed, and multifunctional devices. 相似文献
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Skehel JM Schneider K Murphy N Graham A Benson GM Cutler P Camilleri P 《Electrophoresis》2000,21(12):2540-2545
Apolipoprotein E (ApoE) plays an important role in cholesterol and triglyceride metabolism, being one of the major structural components of chylomicrons and very low density lipoprotein (VLDL) remnants. ApoE functions as a ligand in the receptor-mediated uptake of these remnants from the blood by the liver. A variant form of ApoE, apolipoprotein E*3-Leiden, shows reduced affinity for the low density lipoprotein (LDL) receptor, and results in the dominant expression of type III hyperlipoproteinemia. Two-dimensional electrophoresis (2-DE) has been used to characterise protein expression in serum samples from control and transgenic mice expressing the human ApoE*3-Leiden mutation, fed a cholesterol-rich diet, and transgenic mice fed a normal diet. For the identification of proteins, single silver-stained spots were excised from the 2-DE gels and subjected to in-gel enzymatic digestion. Extracted peptides were analysed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS). This proteomic approach has enabled the ApoE*3-Leiden variant to be positioned in a 2-DE separation of serum proteins, and has identified changes in the expression of haptoglobin, indicating that this protein may provide a marker for the potential onset of atherosclerosis. 相似文献
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David R. Benson Robert Valentekovich Suk-Wah Tam Franois Diederich 《Helvetica chimica acta》1993,76(5):2034-2060
Following a known synthetic procedure, the porphyrin-cyclophane 1 having a porphyrin attached by two straps to an apolar cyclophane binding site was prepared. Upon metallation, the ZnII and FeIII derivatives 2 and 3 , respectively, were obtained in good yields. Treatment of 3 with base yielded the μ-oxo dimer 4 in which the two oxo-bridged porphyrins moieties are both capped by cyclophane binding sites. All compounds 1–4 are freely soluble in protic solvents such as MeOH and CF3CH2OH, and the FeIII derivatives 3 and 4 are active cytochrome P-450 mimics in these protic environments. Strong inclusion complexation of polycyclic aromatic hydrocarbons by 1 and 3 in alcoholic solvents was observed and quantified by 1H-NMR and UV/VIS titrations. Acenaphthylene binds in an ‘equatorial’ orientation which locates its reactive 1,2-double bond near the porphyrin center, whereas phenanthrene binds ‘axially’ with the reactive 9,10-double bond oriented away from the porphyrin. The reduction potential of 3 was not significantly altered by substrate binding. In the unbound form, the FeIII center in porphyrin 3 was found by ESR and 1H-NMR to prefer a high-spin state (S = 5.2). In CF3CH2OH, using iodosylbenzene as O-transfer agent, the FeIII derivative 3 catalyzed the oxidation of acenaphthylene to acenaphthen-1-one ( 14 ). Phenanthrene inhibited the reaction, possibly as a result of strong but nonproductive binding. Under similar conditions, isotetralin ( 18 ) was aromatized with high turnover to 1,4-dihydronaphthalene. The μ-oxo dimer 4 also showed high activity in the oxidation of acenaphthylen in MeOH, a result which provides strong evidence for efficent supramolecular catalysis. Due to as yet unknown reaction channels leading to polymeric products, poor mass balances were generally obtained in the oxidations effected in MeOH and CF3CH2OH in the presence of PhIO. 相似文献
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Let (A) be the coefficient of the second term in the Laurentexpansion about T 1 of the Poincare series p(A, t) of a gradedring A. For a finite extension of integrally closed domains,we prove a formula relating if (B), if (A) and the differentialexponent of B over A. As an application, we prove a conjectureof Carlisle and Kropholler which computes for rings of modularinvariants of finite groups in terms of stabilizers of hyperplanes. 相似文献
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