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971.
Ilya Kuselman 《Accreditation and quality assurance》2009,14(10):575-576
News and Announcements
Guidelines for CITAC projects and CITAC procedure for support of conferences and workshops 相似文献972.
Ilya Shapiro 《Advances in Mathematics》2009,220(6):1657-1688
973.
Pobelov IV Mészáros G Yoshida K Mishchenko A Gulcur M Bryce MR Wandlowski T 《J Phys Condens Matter》2012,24(16):164210
We describe a new setup for simultaneous measurements of force and current in conductive nanocontacts in a liquid environment with a high sampling rate and resolution. A lab-built current-to-voltage converter allows measurements of the current over seven orders of magnitude. As examples, we studied conductances and mechanical forces upon formation and breaking of gold atomic contacts and of two molecular junctions containing 1,2-di(4-pyridyl)ethyne (M1) and 1,4-di(4-pyridyl)buta-1,3-diyne (M2). We found that the forces required to deform or break gold atomic contacts depend critically on the surrounding medium. Further, they show non-linear behaviour in dependence of the number N of gold atoms detached. The electromechanical properties of the two types of molecular junctions upon stretching were analysed by correlating breaking forces with simultaneously measured junction conductances. A rather complex behaviour in a wide range of forces was discovered. Comparison of the current-probe atomic force microscopy experiments on the rupture of molecular junctions with STM-based break junction experiments enables the assignment of breaking forces of molecular junctions to the corresponding junction conductances. 相似文献
974.
Ilya V. Ermakov Guy Van der Sande Jan Danckaert 《Communications in Nonlinear Science & Numerical Simulation》2012,17(12):4767-4779
We study semiconductor ring lasers subject to delayed optical feedback from one or two short external cavities. In case of two cavities we consider the feedback strengths and phases to be either symmetric or asymmetric feedback. When feedback is symmetric, the laser operates in a bi-directional continuous wave or periodic regime for most parameter values. Only for some small parameter regions complex dynamics, such as quasi-periodicity and chaos are obtained. When the feedback is asymmetric complex dynamical regimes, including chaos, are obtained in large parameter regions. We explain complex dynamical regimes obtained in both symmetric and asymmetric feedback cases by linear stability of the stationary solutions calculated using DDE-BIFTOOL. 相似文献
975.
The on-axis intensity distribution of a beam generated by a Fresnel axicon (fraxicon) is experimentally and numerically examined and compared to a classical axicon. Monochromatic illumination produces strong oscillations in this distribution due to diffraction from the fraxicon facets combined with shadowing effects. It is shown that by proper selection of the ratio of the illuminating light wavelength to the period of the fraxicon these oscillations can be minimized by exploiting interference. In addition, polychromatic illumination of the fraxicon also permits homogenization of the on-axis intensity with some remaining oscillations at the start of the depth of field which can be reduced by decreasing the period of the fraxicon. 相似文献
976.
We report the first observation (to our best knowledge) of a constant intensity, quasi-Bessel/nondiffracting beam in an absorbing medium generated by a novel optical element, "exicon," or exponential intensity axicon. Such absorption-compensated and diffraction-resistant beams can find applications in illumination, remote sensing, free-space communications, imaging in biological tissues, nonlinear optics, and other situations where absorption and diffraction hinder light propagation. 相似文献
977.
Ilya S. Kritchenkov Vitaliya G. Mikhnevich Victoria S. Stashchak Anastasia I. Solomatina Daria O. Kozina Victor V. Sokolov Sergey P. Tunik 《Molecules (Basel, Switzerland)》2022,27(10)
A series of [Ir(N^C)2(N^N)]+ NIR-emitting orthometalated complexes (1–7) has been prepared and structurally characterized using elemental analysis, mass-spectrometry, and NMR spectroscopy. The complexes display intense phosphorescence with vibrationally structured emission bands exhibiting the maxima in the range 713–722 nm. The DFT and TD DFT calculations showed that the photophysical characteristics of these complexes are largely determined by the properties of the metalating N^C ligands, with their major contribution into formation of the lowest S1 and T1 excited states responsible for low energy absorption and emission, respectively. Emission lifetimes of 1–7 in degassed methanol solution vary from 1.76 to 5.39 µs and show strong quenching with molecular oxygen to provide an order of magnitude lifetime reduction in aerated solution. The photophysics of two complexes (1 and 7) were studied in model physiological media containing fetal bovine serum (FBS) and Dulbecco’s Modified Eagle Medium (DMEM) to give linear Stern-Volmer calibrations with substantially lower oxygen-quenching constants compared to those obtained in methanol solution. These observations were interpreted in terms of the sensors’ interaction with albumin, which is an abundant component of FBS and cell media. The studied complexes displayed acceptable cytotoxicity and preferential localization, either in mitochondria (1) or in lysosomes (7) of the CHO-K1 cell line. The results of the phosphorescence lifetime imaging (PLIM) experiments demonstrated considerable variations of the sensors’ lifetimes under normoxia and hypoxia conditions and indicated their applicability for semi-quantitative measurements of oxygen concentration in living cells. The complexes’ emission in the NIR domain and the excitation spectrum, extending down to ca. 600 nm, also showed that they are promising for use in in vivo studies. 相似文献
978.
Olefin and diene transformations, catalyzed by organoaluminum-activated metal complexes, are widely used in synthetic organic chemistry and form the basis of major petrochemical processes. However, the role of M–(μ-Cl)–Al bonding, being proven for certain >C=C< functionalization reactions, remains unclear and debated for essentially more important industrial processes such as oligomerization and polymerization of α-olefins and conjugated dienes. Numerous publications indirectly point at the significance of M–(μ-Cl)–Al bonding in Ziegler–Natta and related transformations, but only a few studies contain experimental or at least theoretical evidence of the involvement of M–(μ-Cl)–Al species into catalytic cycles. In the present review, we have compiled data on the formation of M–(μ-Cl)–Al complexes (M = Ti, Zr, V, Cr, Ni), their molecular structure, and reactivity towards olefins and dienes. The possible role of similar complexes in the functionalization, oligomerization and polymerization of α-olefins and dienes is discussed in the present review through the prism of the further development of Ziegler–Natta processes and beyond. 相似文献
979.
Zhanna Starkova Valentina Ilyushenkova Nikolay Polovkov Daria Voskressenskaya Ilya Pikovskoi Mikhail Tebenikhin Ella Vtorushina Anastasiia Kanateva Roman Borisov Vladimir Zaikin 《Molecules (Basel, Switzerland)》2022,27(23)
Polycyclic aromatic sulfur-containing compounds are widely distributed in oil, especially in its low-volatile and heavy fractions (resins, asphaltenes), and this dictates the need for their determination when reliable methods for sulfur removing, cleaning and processing oil are developed. In these cases, “soft” ionization mass spectrometry methods, based on electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI), are particularly effective. However, aromatic sulfur-containing compounds have low polarity and cannot be readily ionized by these methods. To overcome the problem, their preliminary conversion into sulfonium salts by the action of alkyl iodides and a silver-containing agent is widely used. In the process of developing more economical derivatization methods, we found a rather unexpected possibility of implementing S-alkylation of organic sulfides with commercial polydialkylsiloxanes (alkyl = CH3 or C2H5) in the presence of triflic acid (CF3SO3H) as a superacid co-alkylating agent. For homologous dibenzothiophenes as a typical model representative of petroleum sulfur-containing aromatic compounds, ESI and MALDI mass spectra exhibited the signals of corresponding S-alkylsulfonium salts with a high signal-to-noise ratio. A rational mechanism for the described chemical transformation is proposed, including the indispensable activation by triflic acid and the cleavage of the Si-C bond. Specific collision-induced dissociation of corresponding S-alkylated sulfonium cations is considered. The applicability of the derivatization approach to the analysis of petroleum products by high-resolution mass spectrometry is demonstrated. 相似文献
980.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献