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991.
992.
Mechanochemical Encapsulation of Fullerenes in Peptidic Containers Prepared by Dynamic Chiral Self‐Sorting and Self‐Assembly
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Dr. Mirosław Gilski Hanna Jędrzejewska Marcin Sztylko Dr. Piotr Cmoch Dr. Aleksander Shkurenko Prof. Mariusz Jaskólski Prof. Agnieszka Szumna 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(9):3148-3155
Molecular capsules composed of amino acid or peptide derivatives connected to resorcin[4]arene scaffolds through acylhydrazone linkers have been synthesized using dynamic covalent chemistry (DCC) and hydrogen‐bond‐based self‐assembly. The dynamic character of the linkers and the preference of the peptides towards self‐assembly into β‐barrel‐type motifs lead to the spontaneous amplification of formation of homochiral capsules from mixtures of different substrates. The capsules have cavities of around 800 Å3 and exhibit good kinetic stability. Although they retain their dynamic character, which allows processes such as chiral self‐sorting and chiral self‐assembly to operate with high fidelity, guest complexation is hindered in solution. However, the quantitative complexation of even very large guests, such as fullerene C60 or C70, is possible through the utilization of reversible covalent bonds or the application of mechanochemical methods. The NMR spectra show the influence of the chiral environment on the symmetry of the fullerene molecules, which results in the differentiation of diastereotopic carbon atoms for C70, and the X‐ray structures provide unique information on the modes of peptide–fullerene interactions. 相似文献
993.
Environmentally sensitive hydrogel functionalized with electroactive and complexing‐iron(III) catechol groups
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Kamil Marcisz Jan Romanski Zbigniew Stojek Marcin Karbarz 《Journal of polymer science. Part A, Polymer chemistry》2017,55(19):3236-3242
Thermoresponsive pNIPA (poly (N‐isopropylacrylamide)) gels modified with dopamine methacrylamide were synthesized using free‐radical polymerization. In this way, the catechol groups were introduced into the polymer network. The presence of dopamine in the gel led to a significant shift in the volume phase transition temperature (VPTT). It was found that hydrogels were electroactive and that oxidation of catechol groups also led to a strong shift in the VPTT. The temperature window, that is, the range of temperature where volume of the gel could be substantially changed by oxidation of the catechol groups, for the gel formed from the polymerization solution containing 5% of the dopamine derivative, was 30–40 °C. Additionally, the influence of Fe3+ ions, which form the most stable complexes with dopamine, on swelling behavior of the gels was investigated at various pH. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3236–3242 相似文献
994.
Continuum Mechanics and Thermodynamics - The investigation concerns local buckling of compressed flanges of axially compressed composite channel columns. Cooperation of the member flange and web is... 相似文献
995.
996.
The aim of the present study was to determine the influence of the winemaking process on the antioxidant potential and content of phenolic compounds and L-ascorbic acid in wines from the fruits of Rosa rugosa. The results obtained in this study clearly indicate that the fruits of the Rosa rugosa are a desirable raw material for the production of fruit wine. The parameters of the technological process of producing wines from rose fruits had a diversified influence on the tested quality characteristics. Aged wines contained phenolics levels of 473–958 mg/100 mL GAE. The final concentrations of ascorbic acid ranged from 61 to 155 mg/100 mL for the different variants of the wine. Wines revealed high antioxidant activity in assay with DPPH. On the basis of the obtained results, it can be assumed that all the applied variants of the winemaking process are suitable for rose fruit wine. Each variant ensured at least the stability of the antioxidant capacity. 相似文献
997.
Dr. Justyna Kalisz Dr. Wojciech Nogala Dr. Wojciech Adamiak Mateusz Gocyla Prof. Hubert H. Girault Prof. Marcin Opallo 《Chemphyschem》2021,22(13):1352-1360
H2O2 is a versatile chemical and can be generated by the oxygen reduction reaction (ORR) in proton donor solution in molecular solvents or room temperature ionic liquids (IL). We investigated this reaction at interfaces formed by eleven hydrophobic ILs and acidic aqueous solution as a proton source with decamethylferrocene (DMFc) as an electron donor. H2O2 is generated in colorimetrically detectable amounts in biphasic systems formed by alkyl imidazolium hexafluorophosphate or tetraalkylammonium bis(trifluoromethylsulfonyl)imide ionic liquids. H2O2 fluxes were estimated close to liquid|liquid interface by scanning electrochemical microscopy (SECM). Contrary to the interfaces formed by hydrophobic electrolyte solution in a molecular solvent, H2O2 generation is followed by cation expulsion to the aqueous phase. Weak correlation between the H2O2 flux and the difference between DMFc/DMFc+ redox potential and 2 electron ORR standard potential indicates kinetic control of the reaction. 相似文献
998.
We present general analytical expressions for the matrix elements of the atom–diatom interaction potential, expanded in terms of Legendre polynomials, in a basis set of products of two spherical harmonics, especially significant to the recently developed adiabatic variational theory for cold molecular collision experiments [J. Chem. Phys. 143, 074114 (2015); J. Phys. Chem. A 121, 2194 (2017)]. We used two approaches in our studies. The first involves the evaluation of the integral containing trigonometric functions with arbitrary powers. The second approach is based on the theorem of addition of spherical harmonics.
相似文献999.
Microchimica Acta - We report on a new electrochemical sensor for Concanavalin A. It is based on blocking the surface of plasticized PVC membranes that were covalently modified with D-mannose using... 相似文献
1000.