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991.
High-performance numerical algorithms and software for subspace-based linear multivariable system identification 总被引:1,自引:0,他引:1
Vasile Sima Diana Maria Sima Sabine Van Huffel 《Journal of Computational and Applied Mathematics》2004,170(2):371-397
Basic algorithmic and numerical issues involved in subspace-based linear multivariable discrete-time system identification are described. A new identification toolbox—SLIDENT—has been developed and incorporated in the freely available Subroutine Library in Control Theory (SLICOT). Reliability, efficiency, and ability to solve industrial identification problems received a special consideration. Two algorithmic subspace-based approaches (MOESP and N4SID) and their combination, and both standard and fast techniques for data compression are provided. Structure exploiting algorithms and dedicated linear algebra tools enhance the computational efficiency and reliability. Extensive comparisons with the available computational tools based on subspace techniques show the better efficiency of the SLIDENT toolbox, at comparable numerical accuracy, and its capabilities to solve identification problems with many thousands of samples and hundreds of parameters. 相似文献
992.
C. Remzi Becer Sabine Hahn Martin W. M. Fijten Hanneke M. L. Thijs Richard Hoogenboom Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2008,46(21):7138-7147
Homopolymers of methacrylic acid (MAA), monoethyleneglycol methyl ether methacrylate (MEOMA), diethyleneglycol methyl ether methacrylate (MEO2MA), oligo(ethyleneglycol) methyl ether methacrylate (OEGMA475 and OEGMA1100) and oligo(ethyleneglycol) ethyl ether methacrylate (OEGEMA246) were synthesized with various chain lengths via reversible addition fragmentation chain transfer (RAFT) polymerization. The homopolymers of MAA, MEOMA and OEGMA1100 did not show any cloud point (CP) in the range of 0–100 °C, whereas at a pH value of 7, the CPs were found to be 20.6, 93.7, and 20.0 °C for p(MEO2MA), p(OEGMA475) and p(OEGEMA246), respectively, with an initial monomer to initiator ratio of 50. Furthermore, statistical copolymer libraries of MAA with OEGMA475 and OEGMA1100 were prepared. The cloud points of the random copolymers of MAA and OEGMA475 were found to be in the range of 20–90 °C; surprisingly, even though the homopolymers of MAA and OEGMA1100 did not exhibit any LCST behavior, the copolymers of these monomers at certain molar ratios (up to 40% OEGMA1100) revealed a double responsive behavior for both temperature and pH. Finally, the cloud points were found to be in the range of 22–98 °C, measured at pH values of 2, 4, and 7, while no cloud point was detected at pH 10. © Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7138–7147, 2008 相似文献
993.
994.
Dr. Paloma Vidal Dr. Virginia Roldós Dr. María del Carmen Fernández‐Alonso Dr. Boris Vauzeilles Prof. Dr. Yves Bleriot Prof. Dr. F. Javier Cañada Dr. Sabine André Prof. Dr. Hans‐Joachim Gabius Prof. Dr. Jesús Jiménez‐Barbero Dr. Juan Félix Espinosa Dr. Sonsoles Martín‐Santamaría 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(43):14581-14590
The human lectin galectin‐1 (hGal‐1) translates sugar signals, that is, β‐galactosides, into effects on the level of cells, for example, growth regulation, and has become a model for studying binding of biopharmaceutically relevant derivatives. Bound‐state conformations of Galβ‐C‐(1→3)‐Glcβ‐OMe ( 1 ) and its βGal‐(1→3)‐βGlc‐OMe disaccharide parent compound were studied by using NMR spectroscopy (transferred (TR)‐NOESY data), assisted by docking experiments and molecular dynamics (MD) simulations. The molecular recognition process involves a conformational selection event. Although free C‐glycoside access four distinct conformers in solution, hGal‐1 recognizes shape of a local minimum of compound 1 , the syn‐Φ/syn‐Ψ conformer, not the structure at global minimum. MD simulations were run to explain, in structural terms, the observed geometry of the complex. 相似文献
995.
Dipl.‐Chem. Markus Mansueto Dr. Wolfgang Frey Prof. Dr. Sabine Laschat 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(47):16058-16065
Novel chiral amino acid derived ionic liquid crystals with amine and amide moieties as spacers between the imidazolium head group and the alkyl chain were synthesised. The key step in the synthesis utilised the relatively uncommon SO3 leaving group in a microwave‐assisted reaction. The mesomorphic properties of the mesogens were determined by differential scanning calorimetry (DSC), polarising optical microscopy (POM) and X‐ray diffraction. All liquid crystalline salts exhibit a smectic A mesophase geometry with strongly interdigitated bilayer structures. An increase of the steric bulk of the stereogenic centre hindered the formation of mesophases. In case of phenylalanine‐derived derivatives a mesomorphic behaviour was observed for shorter alkyl chains as compared to other amino acid derivatives indicating an additional stabilising effect by the phenyl moiety. 相似文献
996.
Sabine Löw Jonathan Becker Christian Würtele Andreas Miska Dr. Christian Kleeberg Prof. Dr. Ulrich Behrens Dr. Olaf Walter Prof. Dr. Siegfried Schindler 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(17):5342-5351
Mixing CuCl2 ? 2 H2O with benzylamine in alcoholic solutions led to an extremely colorful chemistry caused by the formation of a large number of different complexes. Many of these different species could be structurally characterized. These include relatively simple compounds such as [Cu(L1)4Cl2] (L1=benzylamine) and (HL1)2[CuCl4]. Most interestingly is the easy formation of two cluster complexes, one based on two cluster units Cu4OCl6(L1)4 connected through one [Cu(L1)2Cl2] complex and one based on a cubane‐type cluster ([Cu4O4](C11H14)4Cl4). Both clusters proved to be highly reactive in a series of oxidation reactions of organic substrates by using air or peroxides as oxidants. Furthermore, it was possible to isolate and structurally characterize ([Cu(L1)Cl]3 and [Cu(benz2mpa)2]CuCl2 (benz2mpa=benzyl‐(2‐benzylimino‐1‐methyl‐propylidene)‐amine), two copper(I) complexes that formed in solution, demonstrating the high redox activity of the cluster systems. In addition, it was possible to solve the molecular structures of the compounds Cu4OCl6(MeOH)4, [Cu(MeOH)2Cl2], [Cu(aniline)2Cl2], and an organic side product (HC13H19NOCl). In fact all determined structures are of a known type but the chemical relation between these compounds could be explained for the first time. The paper describes these different compounds and their chemical equilibria. Some of these complexes seem to be relevant in catalytic oxidation reactions and their reactivity is discussed in more detail. 相似文献
997.
Julius A. Knöller Guoyun Meng Dr. Xiang Wang David Hall Anton Pershin Prof. Dr. David Beljonne Dr. Yoann Olivier Prof. Dr. Sabine Laschat Prof. Dr. Eli Zysman‐Colman Prof. Dr. Suning Wang 《Angewandte Chemie (International ed. in English)》2020,59(8):3156-3160
New symmetric and unsymmetric B,N,B‐doped benzo[4]helicenes 3 – 6 a/b have been achieved in good yields, using a three‐step process, starting from N(tolyl)3 in a highly divergent manner (7 examples). A borinic acid functionalized 1,4‐B,N‐anthracene 1 was found to display unprecedented reactivity, acting as a convenient and highly effective precursor for selective formation of bromo‐substituted B,N,B‐benzo[4]helicenes 2 a / 2 b via intramolecular borylation and sequential B?Mes bond cleavage in the presence of BBr3. Subsequent reaction of 2 a / 2 b with Ar‐Li provided a highly effective toolbox for the preparation of symmetrically/unsymmetrically functionalized B,N,B‐helicenes. Their high photoluminescence quantum yields along with the small ΔEST suggest their potential as thermally activated delayed fluorescence (TADF) emitters for organic light‐emitting diodes (OLEDs). 相似文献
998.
Jhe‐Hao Li Joonseok Oh Sabine Kienesberger Nam Yoon Kim David J. Clarke Ellen L. Zechner Jason M. Crawford 《Angewandte Chemie (International ed. in English)》2020,59(41):17872-17880
Leupeptin is a bacterial small molecule that is used worldwide as a protease inhibitor. However, its biosynthesis and genetic distribution remain unknown. We identified a family of leupeptins in gammaproteobacterial pathogens, including Photorhabdus, Xenorhabdus, and Klebsiella species, amongst others. Through genetic, metabolomic, and heterologous expression analyses, we established their construction by discretely expressed ligases and accessory enzymes. In Photorhabdus species, a hypothetical protein required for colonizing nematode hosts was established as a new class of proteases. This enzyme cleaved the tripeptide aldehyde protease inhibitors, leading to the formation of “pro‐pyrazinones” featuring a hetero‐tricyclic architecture. In Klebsiella oxytoca, the pathway was enriched in clinical isolates associated with respiratory tract infections. Thus, the bacterial production and proteolytic degradation of leupeptins can be associated with animal colonization phenotypes. 相似文献
999.
The propagation kinetics of isoprene radical polymerizations in bulk and in solution are investigated via pulsed laser initiated polymerizations and subsequent polymer analyses via size‐exclusion chromatography, the PLP‐SEC method. Because of low polymerization rate and high volatility of isoprene, the polymerizations are carried out at elevated pressure ranging from 134 to 1320 bar. The temperatures are varied between 55 and 105 °C. PLP‐SEC yields activation parameters of kp (Arrhenius parameters and activation volume) over a wide temperature and pressure range that allow for the calculation of kp at technically relevant ambient pressure conditions. The kp values determined are very low, e.g., 99 L mol?1 s?1 at 50 °C, which is even lower than the corresponding value for styrene polymerizations. The presence of a polar solvent results in a slight increase of kp compared to the bulk system. The kp values reported are important for determining rate coefficients of other elemental reactions from coupled parameters as well as for modeling isoprene free‐radical polymerizations and reversible deactivation radical polymerization with respect to tailored polymer properties and optimizing the polymerization processes. 相似文献
1000.
Johanna Frey Dr. Alaleh Malekafzali Isabel Delso Dr. Sabine Choppin Prof. Françoise Colobert Dr. Joanna Wencel-Delord 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(23):8929-8933
N−C axially chiral compounds have emerged recently as appealing motifs for drug design. However, the enantioselective synthesis of such molecules is still poorly developed and surprisingly no metal-catalyzed atroposelective N-arylations have been described. Herein, we disclose an unprecedented Cu-catalyzed atroposelective N−C coupling that proceeds at room temperature. Such mild reaction conditions, which are a crucial parameter for atropostability of the newly generated products, are operative thanks to the use of hypervalent iodine reagents as a highly reactive coupling partners. A large panel of the N−C axially chiral compounds was afforded with very high enantioselectivity (up to >99 % ee) and good yields (up to 76 %). Post-modifications of thus accessed atropisomeric compounds allows further expansion of the diversity of these appealing compounds. 相似文献