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71.
A supported nanoliquid membrane was developed to improve the separation of rare metal ion gadolinium (Gd) from nitrate solution medium. The nanoliquid membrane was prepared by dispersion of nanoparticles in organic phase and Aliquat 336 was applied as the carrier. TiO2 and SiO2 as hydrophobic and hydrophilic nanoparticles were effectively incorporated in the supported liquid membrane (SLM) system and the effect of size, concentration, and type of nanoparticle in the SLM were evaluated. A membrane phase of 0.015 M Aliquat-336 in kerosene and 0.04 wt% of SiO2 with the size of 15 nm was found to have the highest permeability coefficient of 12.57?×?10?5 m/s and enhanced the permeability coefficient by 28.2%. Hydrophobicity and hydrophilicity of the nanoparticles were observed to have remarkable effects on the permeation of the SLM system and concluded that the hydrophobic nanoparticle was more desirable. Results showed that the solid supported pore’s blockage and aggregation of nanoparticles could bring adverse effects at a high nanoparticle concentration at this SLM configuration. The stability tests were conducted over ten cycles of separation and the supported nanoliquid membrane had slight reduction of permeation during the test. 相似文献
72.
MoS2‐on‐MXene Heterostructures as Highly Reversible Anode Materials for Lithium‐Ion Batteries 下载免费PDF全文
Chi Chen Dr. Xiuqiang Xie Prof. Babak Anasori Asya Sarycheva Dr. Taron Makaryan Dr. Mengqiang Zhao Patrick Urbankowski Prof. Ling Miao Prof. Jianjun Jiang Prof. Yury Gogotsi 《Angewandte Chemie (International ed. in English)》2018,57(7):1846-1850
Two‐dimensional (2D) heterostructured materials, combining the collective advantages of individual building blocks and synergistic properties, have spurred great interest as a new paradigm in materials science. The family of 2D transition‐metal carbides and nitrides, MXenes, has emerged as an attractive platform to construct functional materials with enhanced performance for diverse applications. Here, we synthesized 2D MoS2‐on‐MXene heterostructures through in situ sulfidation of Mo2TiC2Tx MXene. The computational results show that MoS2‐on‐MXene heterostructures have metallic properties. Moreover, the presence of MXene leads to enhanced Li and Li2S adsorption during the intercalation and conversion reactions. These characteristics render the as‐prepared MoS2‐on‐MXene heterostructures stable Li‐ion storage performance. This work paves the way to use MXene to construct 2D heterostructures for energy storage applications. 相似文献
73.
Zheng T Narayan RS Schomaker JM Borhan B 《Journal of the American Chemical Society》2005,127(19):6946-6947
A simple and efficient process to cyclize triols containing a 1,2-diol functionality with a pendant hydroxyl group is presented. The one-pot procedure converts the 1,2-diol into an ortho ester in situ, which upon treatment with a Lewis acid generates a cyclic acetoxonium intermediate. This intermediate is subsequently trapped by the pendant hydroxyl group to generate a cyclic ether. The stereochemistry of the 1,2-diol is transferred to the product with complete fidelity (inversion at the site of cyclization), and the reaction proceeds with high regioselectivity. The process is akin to the Lewis acid-catalyzed intramolecular ring-opening of epoxides with hydroxyl groups yielding cyclic ethers of various sizes with regio- and stereochemical control. 相似文献
74.
75.
Alumina supported ammonium fluoride was found as an efficient reagent for the synthesis of 1,2,4‐oxadi‐azoles of amidoximes under solvent free conditions using microwave irradiation. This method is a one‐pot, easy, rapid, and high‐yielding reaction for the synthesis of 1,2,4‐oxadiazole derivatives from amidoximes and acyl chlorides. Reaction of amidoximes with acylchlorides in the presence of alumina without ammonium fluoride gave only the corresponding O‐acylamidoximes as major product. 相似文献
76.
H. Michael Mack Everette A. Davis Babak Kadkhodayan Richard A. Taylor Dean C. Duncan Charles F. Beam 《Journal of heterocyclic chemistry》1987,24(6):1733-1739
C(α),O-Dilithiooximes, C(α),N-dilithiobenzoylhydrazones, or C(α),N-dilithiocarboalkoxyhydrazones were prepared in an excess of lithium diisopropylamide (LDA) and condensed with 2-aminobenzophenones, or isatoic anhydrides to give intermediates that were treated with aqueous acid, which caused their hydrolysis, cyclodehydration and/or linear dehydration to give products which were substituted quinolines or related fused-ring heterocycles (e.g., cycloheptaquinolines). Dilithiobenzoylacetone was condensed with 2-aminobenzophenones, which was followed by acid cyclodehydration to substituted 2-phenacylquinolines. 相似文献
77.
Stability and rheological properties of concentrated emulsions (including those for manufacture of vitamin microcapsules) can be related to elementary coalescence acts and adhesion of emulsion drops interacting through thin layers (microscopic emulsion films) of a dispersion medium A new procedure was used for measuring the adhesion force fa between two drops of n-heptane in polymer solutions and lifetime τ of the drops in the contacts depending on the volume concentration C of the polymer, time of formation tf of adsorption layers, temperature T, capillary pressure Pc in the film, surface area S of the film, and on addition of acetone and tannin. The molecular mechanism of the interaction between adsorption layers of polymers and of the process of film destruction is discussed on the basis of the relationships obtained for interaction free energy Δ Fa, activation energy E, destruction activation volume δ and physico-chemical parameters. 相似文献
78.
A series of 37 peptides containing an iodo-aryl amide active site were generated by means of both solid phase and conventional synthesis. These peptides were screened for asymmetric induction in the bromolactonization of 4-phenyl-4-pentenoic acid based on the generation of chiral bromoiodinane bromenium sources. The study culminated in the discovery of a tri-peptide iodo-aryl amide that effected the desired bromolactonization in quantitative conversion with 24% ee. The experiments disclosed herein provided valuable insight that ultimately facilitated the development of more synthetically useful enantioselective halocyclization methodology. 相似文献
79.
Babak Kaboudin Foad Kazemi Abolfazl Ghaderian Zahra Zand 《Journal of the Iranian Chemical Society》2014,11(4):1121-1127
80.
A highly efficient photocatalytic reduction of nitroarenes using TiO2/polyethylene glycol 400-water (TiO2/PEG–H2O) is reported. This system at deoxygenated and illuminated (sunlight or violet LED) conditions efficiently reduced nitroarenes using oxalic acid or ammonium formate as a sacrificial electron donor. Reducible functional groups such as chloro, hydroxy, flouro, bromo and carbonyl were intact under the optimized reaction conditions. The 0.1 and 0.5–1 mmol amount of nitroarenes was used under sunlight and violet LED (400 nm) irradiation, respectively. Reusability of the nanotitania was successfully carried out four times. The analyses of the recovered catalyst after five runs including TEM, XRD, TGA and CHN were done and results showed that PEG is located on TiO2; no change in morphology, crystallinity and particle sizes was observed. 相似文献