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排序方式: 共有695条查询结果,搜索用时 15 毫秒
61.
Christian Wenz Coral Barbas Ángeles López‐Gonzálvez Antonia Garcia Fernando Benavente Victoria Sanz‐Nebot Tim Blanc Gordon Freckleton Philip Britz‐McKibbin Meera Shanmuganathan Francois de l′Escaille Johann Far Rob Haselberg Sean Huang Carolin Huhn Martin Pattky David Michels Si Mou Feng Yang Christian Neusuess Nora Tromsdorf Edward E.K. Baidoo Jay D. Keasling SungAe Suhr Park 《Journal of separation science》2015,38(18):NA-NA
A collaborative study on the robustness and portability of a capillary electrophoresis‐mass spectrometry method for peptide mapping was performed by an international team, consisting of 13 independent laboratories from academia and industry. All participants used the same batch of samples, reagents and coated capillaries to run their assays, whereas they utilized the capillary electrophoresis‐mass spectrometry equipment available in their laboratories. The equipment used varied in model, type and instrument manufacturer. Furthermore, different types of sheath‐flow capillary electrophoresis–mass spectrometry interfaces were used. Migration time, peak height and peak area of ten representative target peptides of trypsin‐digested bovine serum albumin were determined by every laboratory on two consecutive days. The data were critically evaluated to identify outliers and final values for means, repeatability (precision within a laboratory) and reproducibility (precision between laboratories) were established. For relative migration time the repeatability was between 0.05 and 0.18% RSD and the reproducibility between 0.14 and 1.3% RSD. For relative peak area repeatability and reproducibility values obtained were 3–12 and 9–29% RSD, respectively. These results demonstrate that capillary electrophoresis‐mass spectrometry is robust enough to allow a method transfer across multiple laboratories and should promote a more widespread use of peptide mapping and other capillary electrophoresis‐mass spectrometry applications in biopharmaceutical analysis and related fields. 相似文献
62.
Microwave‐Assisted Catalyst Free Three Component Synthesis of Mono and Bis Spiro Pyrazolopyridines in Solvent Free Reaction 下载免费PDF全文
Mohammad Nikpassand Leila Zare Fekri Neda Jamshidi 《Journal of heterocyclic chemistry》2015,52(5):1580-1583
Multicomponent synthesis of mono and bis‐spiro pyrazolopyridines from isatin derivatives, indanedione, and 3‐methyl‐5‐aminopyrazole under microwave irradiation in the absence of any catalyst or solvent with high yield and short reaction time is reported. 相似文献
63.
Genetic diversity and haplotype structure of 21 Y‐STRs,including nine noncore loci,in South Tunisian Population: Forensic relevance 下载免费PDF全文
Faten Makki‐Rmida Arwa Kammoun Nadia Mahfoudh Adnene Ayadi Abdullah Ahmed Gibriel Bakhta Mallek Leila Maalej Zouheir Hammami Samir Maatoug Hafedh Makni Saber Masmoudi 《Electrophoresis》2015,36(23):2908-2913
Y chromosome STRs (Y‐STRs) are being used frequently in forensic laboratories. Previous studies of Y‐STR polymorphisms in different groups of the Tunisian population identified low levels of diversity and discrimination capacity (DC) using various commercial marker sets. This definitely limits the use of such systems for Y‐STRs genotyping in Tunisia. In our investigation on South Tunisia, 200 unrelated males were typed for the 12 conventional Y‐STRs included in the PowerPlex® Y System. Additional set of nine noncore Y‐STRs including DYS446, DYS456, DYS458, DYS388, DYS444, DYS445, DYS449, DYS710, and DYS464 markers were genotyped and evaluated for their potential in improving DC. Allele frequency, gene diversity, haplotype diversity (HD), and DC calculation revealed that DYS464 was the most diverse marker followed by DYS710 and DYS449 markers. The standard panel of 12 Y‐STRs (DC = 80.5%) and the nine markers were combined to obtain DC of 99%. Among the 198 different haplotypes observed, 196 haplotypes were unique (HD = 99.999). Out of the nine noncore set, six Y‐STRs (DYS458, DYS456, DYS449, DYS710, DYS444, and DYS464) had the greatest impact on enhancing DC. Our data provided putative Y‐STRs combination to be used for genetic and forensic applications. 相似文献
64.
Bahare Sadeghi Far Gholamhossein Grivani Aliakbar Dehno Khalaji Mahdi Khorshidi Václav Eigner Michal Dušek 《Journal of Cluster Science》2017,28(6):3217-3227
New centrosymmetric trinuclear zinc(II) complex {[Zn(μ-ONN)(μ2-O)(μ-OO)]2Zn} has been synthesized by the reaction of a potentially ONN tridentate Schiff base ligand, and N,N-dimethylethylendiamin, with Zn(OAc)2·2H2O in methanol, in the refluxed conditions and characterized by elemental analysis, FT-IR and UV–Vis spectroscopy. Single crystal X-ray structure analysis reveals a trinuclear complex {[Zn(μ-ONN)(μ2-O)(μ-OO)]2Zn} with zinc(II) ions connected by three different bridges, (μ-ONN) of the Schiff base ligand, μ2-O and μ-OO of the acetate. The complex is centrosymmetric, with one of the Zn atoms located at the inversion center. While the central Zn(II) ion is six-coordinated, the coordination number of the other Zn(II) ions is five. Finally, the {[Zn(μ-ONN)(μ2-O)(μ-OO)]2Zn} complex was thermally decomposed in air at 700 °C resulted in ZnO nano crystalites with the average size of 42 nm. The antibacterial activity of ligand and its zinc(II) complex were tested against gram-positive and gram-negative bacteria. The ligand showed higher activity than its zinc(II) complex. 相似文献
65.
Leila Goudarzi 《代数通讯》2017,45(9):4093-4098
Let L be a finite dimensional Lie algebra. Then for a maximal subalgebra M of L, a 𝜃-completion for M is a subalgebra C of L such that CM and ML?C and C∕ML contains no non-zero ideal of L∕ML, properly. And a 𝜃-completion C of M is said to be a strong 𝜃-completion, if C = L or there exists a subalgebra B of L such that C be maximal in B and B is not a 𝜃-completion for M. These are analogous to the concepts of 𝜃-completion and strong 𝜃-completion of a maximal subgroup of a finite group. Now, we consider the influence of these concepts on the structure of a finite dimensional Lie algebra. 相似文献
66.
Maha Chaieb Héla Habli Leila Mejrissi Brahim Oujia Florent Xavier Gadéa 《International journal of quantum chemistry》2014,114(11):731-747
A wide adiabatic study is performed for NaRb molecule, involving 151Σ+ electronic states including the ionic state Na?Rb+, as well as 143Σ+, 1–91,3Π, and 1–51,3Δ states. This investigation is performed using an ab initio approach which involves the effective core potential, the core polarization potential with l‐dependent cut‐off functions. The NaRb system has been treated as a two‐electron system and the full valence configuration interaction is easily achieved. The spectroscopic constants Re, De, Te, ωe, ωexe, Be, and D0 for all these states are derived. We have also computed the vibrational levels as well their spacing for different values of J. In addition, permanent and transition dipole moments are determined and analyzed. The Dunham coefficients have been used to perform experimental spacing to compare directly with our results. The present calculations on NaRb extend previous theoretical works to numerous electronic excited states in the various symmetries. © 2014 Wiley Periodicals, Inc. 相似文献
67.
68.
A simple and efficient one-pot approach for assembling some fused spiro[4H-pyran-oxindole] heterocycles by means of three-component reactions between isatins, malononitrile or ethyl cyano-acetate, and 1,3-dicarbonyl compounds is reported. The combinatorial syntheses were achieved for the first time without applying extra activation energy at ambient temperature while making use of [BMIm]BF4 as an ionic liquid catalyst. Good functional group tolerance and broad scope of usable substrates are other prominent features of the present methodology. 相似文献
69.
Mahmoudi L Mohajer D Kissner R Koppenol WH 《Dalton transactions (Cambridge, England : 2003)》2011,40(34):8695-8700
Manganese(III)-meso-tetraphenylporphyrin [Mn(TPP)] and manganese(III)-meso-tetrakis(pentafluorophenyl)porphyrin [Mn(TPFPP)] catalyse the epoxidation of cyclooctene by IO(4)(-) in the presence of excess imidazoles, in both dry CH(2)Cl(2) and CH(2)Cl(2) saturated with H(2)O. The reaction rates of the electron deficient Mn(TPFPP) are a factor 24 less than those of Mn(TPP); however, the former increases 15-30 times in the presence of water, while those of Mn(TPP) do so by a factor of 2-3. The most striking catalytic enhancement caused by the addition of water was observed with 2-methylimidazole and Mn(TPFPP). As deprotonation of imidazoles may play a significant role in the presence of water, we found that manganese(III)-meso-tetrakis(phenyl-4-sulfonato)porphyrin [Mn(TPPS)] decreases the NH proton pK(a) of axially coordinated imidazole from 14.2 to 9.5. We conclude that the imidazole ligand is partially deprotonated in the presence of water. The latter enables the solvation of imidazolium ions that are formed simultaneously. The imidazolate form of the co-catalyst is a much stronger donor than the imidazole itself, providing electron density to Mn(III) and thus promoting oxygen transfer. The failure of N-methylimidazole to increase the reaction rates upon addition of water supports this hypothesis. A functionally related deprotonation has been shown to occur in horseradish peroxidase (J. S. de Ropp, V. Thanabal, G. N. La Mar, J. Am. Chem. Soc. 1985, 107, 8270-8272) and in chlorite dismutase (B. R. Goblirsch, B. R. Streit, J. L. Dubois, C. M. Wilmot, J. Biol. Inorg. Chem. 2010, 15, 879-888). Mn(III)porphyrins in combination with imidazoles and water constitute a functional biomimetic model of peroxidases. 相似文献
70.
Rivera A Farías T de Ménorval LC Autié-Castro G Yee-Madeira H Contreras JL Autié-Pérez M 《Journal of colloid and interface science》2011,360(1):220-226
The employment of an acid natural clinoptilolite (AZH-1) in the adsorption and separation of n-paraffins has been evaluated. Natural clinoptilolite, NZ, was the raw material used to prepare the sodium-exchanged clinoptilolite (AZ) starting from which the AZH-1 sample was obtained by acid treatment. The structural stability of the samples after the applied treatments was demonstrated. The nitrogen adsorption experiments indicated that the acid sample has a homogeneous porous distribution and a considerable increase in the micropore volume with respect to NZ and AZ. The employment of the inverse gas chromatography at infinite dilution (IGCID) allowed studying the adsorption and separation of n-paraffin mixtures on AZH-1. It was also confirmed that the diffusion on AZH-1 took place in an unblocked structure through the A channel of ten members with minimal interactions. The IGCID results demonstrated the capacities of the acid Cuban natural zeolite in the adsorption and separation of n-paraffin mixtures. 相似文献