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131.
《合成通讯》2013,43(8):1067-1076
Abstract The Gabriel–Cromwell method is applied successfully in the synthesis of ferrocenyl‐substituted aziridines. Acryloyl‐ and crotonoylferrocenes are brominated first and then reacted with benzylamine, diisopropylamine, and furfurylamine in the presence of triethylamine. The aziridines are obtained in more than 90% isolated yields. 相似文献
132.
Globular proteins exhibit dielectrophoresis (DEP) responses in experiments where the applied field gradient factor ∇E2 appears far too small, according to standard DEP theory, to overcome dispersive forces associated with the thermal energy kT of disorder. To address this a DEP force equation is proposed that replaces a previous empirical relationship between the macroscopic and microscopic forms of the Clausius–Mossotti factor. This equation relates the DEP response of a protein directly to the dielectric increment δε+ and decrement δε− that characterize its β-dispersion at radio frequencies, and also indirectly to its intrinsic dipole moment by way of providing a measure of the protein's effective volume. A parameter Γpw, taken as a measure of cross-correlated dipole interactions between the protein and its water molecules of hydration, is included in this equation. For 9 of the 12 proteins, for which an evaluation can presently be made, Γpw has a value of ≈4600 ± 120. These conclusions follow an analysis of the failure of macroscopic dielectric mixture (effective medium) theories to predict the dielectric properties of solvated proteins. The implication of a polarizability greatly exceeding the intrinsic value for a protein might reflect the formation of relaxor ferroelectric nanodomains in its hydration shell. 相似文献
133.
Steffen Maier Nikolai Hippchen Dr. Frank Rominger Dr. Jan Freudenberg Prof. Uwe H. F. Bunz 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(66):16320-16324
The synthesis of novel (N−)acene-based cyclooligomers is reported. Glaser-Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel-permeation chromatographies. For the diazatetracene, the use of sec-butyl-silylethynyl groups is necessary to achieve solubility. Diazatetracene-based cyclodimers and cyclotrimers were used as semiconductors in thin-film transistors. Although their optoelectronic properties are quite similar, their electron mobilities in proof-of-concept thin-film transistors differ by an order of magnitude. 相似文献
134.
Induced twisted-grain-boundary phases in the binary mixtures of a cholesteric and a nematic compound
Thermodynamical, optical-texture and dielectric studies have been performed to study the phase diagram of the binary system of 5-cholesten-3β-ol-octanoate and 4-n-nonyloxybenzoic acid. It is observed that low concentrations of 5-cholesten-3β-ol-octanoate (2–30?mol?%) in 4-n-nonyloxybenzoic acid induce a mean-field phase diagram derived by Renn within the framework of the chiral Chen–Lubenski model. Various optical textures of the twisted-grain-boundary (TGB) phases under different conditions of molecular anchoring have been observed. Weak transitions related to the TGB phases have been detected by temperature dependent dielectric spectroscopy. 相似文献
135.
C.M. da Fonseca Dan A. Mazilu Irina Mazilu H. Thomas Williams 《Applied Mathematics Letters》2013,26(12):1206-1211
A straightforward model for deposition and evaporation on discrete cells of a finite array of any dimension leads to a matrix equation involving a Sylvester–Kac type matrix. The eigenvalues and eigenvectors of the general matrix are determined for an arbitrary number of cells. A variety of models to which this solution may be applied are discussed. 相似文献
136.
The interaction between two parallel charged plates in ionic solution is a general starting point for studying colloidal complexes. An intuitive expression of the pressure exerted on the plates is usually proposed, which includes an electrostatic plus an osmotic contribution. We present here an explicit and self-consistent derivation of this formula in the only framework of the Poisson–Boltzmann (PB) theory. We also show that, depending on external constraints, the correct thermodynamic potential can differ from the usual PB free energy. For asymmetric, oppositely charged plates, the resulting expression predicts a non-trivial equilibrium position with the plates separated by a finite distance. The depth of this energy minimum is decisive for the stability of the complex. It is therefore crucial to obtain its explicit dependence on the charge densities of the plates and on the ion concentration. Analytic expressions for the position and depth of the energy minimum were derived in 1975 by Ohshima [Colloid Polym. Sci. 253, 150 (1975)] but, surprisingly, these important results seem to have been overlooked. We retrieve these expressions in a simpler formalism, more familiar to the physics community, and give a physical interpretation of the observed behavior. 相似文献
137.
Vinzenz Thönnißen Prof. Dr. Frederic W. Patureau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(25):7189-7192
The atroposelective formation of C−N bonds has recently emerged within the field of amination reactions. On first sight, it may seem quite surprising that such an ancient class of organic coupling reactions (Gabriel, Ullmann, Goldberg, Buchwald, Hartwig and many others) has so few enantioselective solutions, and this in spite of asymmetric synthesis being now a mature concept and field. Why should enantioselective C−N bond formation be so difficult? This question and some of the first examples that promise an imminent change of paradigm are herein discussed. 相似文献
138.
Leslie W. Deady Andrew B. Hughes Indumathy B. Mahadevan Nurul H. Quazi Leann M. Tilley 《合成通讯》2013,43(5):803-820
The synthesis of fluorescent 2,10-derivatives of the title chromophore are described. The substituents contain amino-reactive N-hydroxysuccinimde ester and thiol-reactive iodoacetamide groups for attachment to biomolecules. A phosphate derivative was also prepared as an enzyme substrate. 相似文献
139.
The advent of multiple collector–inductively coupled plasma–mass spectrometry (MC-ICP-MS) has made the high-precision determination of Ge isotopes possible, which leads to the widespread application of Ge isotopes in earth, ocean, and cosmochemistry fields. This paper reviews the history of Ge isotope analysis, chemical dissolution and purification, and mass spectrometry measurements. Concentrated HNO3 is sufficient to dissolve nearly all types of samples and HF is also involved for Si-rich samples. Low-temperature ashing prior to dissolution is an alternative way to preconcentrate Ge in organic-rich samples. For different matrices, Ge isotopes can be determined by MC-ICP-MS coupled with a traditional nebulizer system or hydride generation system after two-step separation, one step cation/anion-exchange separation, or Mg/Fe co-precipitation protocols. Ion-exchange column methods are suitable for samples with elevated matrix and Ge content such as sulfides, iron oxides, silicate rocks, and coals, whereas Mg or Fe coprecipitation methods are particularly suitable for all kinds of water. Hydride generation systems are improved over traditional nebulizer system due to the smaller sample quantity and fewer matrix-related interferences. Sample-standard bracketing, double spike, and external Ga isotope normalization are used to mass bias correction and yield consistent results. Analytical methods involving Ge-poor samples and Ge isotope analyses based on different Ge species or specific Ge compound in natural environment will be important prospects in the further study. For further applications of Ge isotopes in mineral deposits such as sulfide and iron oxide deposits, sulfides, and iron oxides reference materials should be developed in the future. 相似文献
140.