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991.
992.
Chong Shik Chin Hyungeui Lee Myung Ki Lee Soyoung Noh Min-Sik Eum Seunggweon Hong 《Journal of organometallic chemistry》2005,690(5):1306-1313
Alkyl-carbonyl-iridium [Ir(CH3)(CO)(η2-O2CR′)(PPh3)2]+ (1, R′ = CH3, Ph, p-C6H4CH3) react with alkynes (RCCH; R = Ph, p-C6H4CH3) in the presence of NEt3 to give acyl-alkynyl-iridium Ir(C(O)CH3)(-CCR)(η2-O2CR′)(PPh3)2 (4) which further react with RCCH to give alkyl-carbonyl-cis-bis(alkynyl) iridium Ir(CH3)(CO)(CCR)2(PPh3)2 (5). cis-Bis(alkenyl)iridium complexes, Ir(-CHCH2)2(η2-O2CCH3)(PPh3)2 (6) and (η2-O2CCH3)(PPh3)2 (7) react with substituted alkynes RCCH (R = Ph, p-C6H4CH3, cyclohex-1-enyl) to give cis-bis(alkynyl) Ir(CCR)2(η2-O2CCH3)(PPh3)2 (9) that further react with RCCH to undergo the alkyne insertion reaction into the Ir-O bond to produce iridacycles containing vinyl acetate ligands, (-CCR)2(PPh3)2 (8). 相似文献
993.
Copolymers of N-isopropylacrylamide, 2-hydroxyethyl methacryl lactate [(HEMA)-lactate] and acrylic acid (AAc) were prepared with varying mole ratios of monomers to develop copolymers with gelation properties above a certain concentration for a bioerodible, in-situ gelling material. The copolymers formed gels in situ under physiological condition. The gelation temperature of the copolymers decreased as the HEMA-lactate content of the copolymers increased due to the hydrophobicity of HEMA-lactate, and increased as the AAc content increased due to the hydrophilicity of AAc. The gels redissolve at 37 degrees C as their LCSTs increase above 37 degrees C due to the hydrolysis of the HEMA-lactate pendant groups. 相似文献
994.
Separation of Acetylene from Carbon Dioxide and Ethylene by a Water‐Stable Microporous Metal–Organic Framework with Aligned Imidazolium Groups inside the Channels
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Jaechul Lee Chong Yang Chuah Prof. Jaheon Kim Youngsuk Kim Nakeun Ko Younggyu Seo Prof. Kimoon Kim Prof. Tae Hyun Bae Prof. Eunsung Lee 《Angewandte Chemie (International ed. in English)》2018,57(26):7869-7873
Separation of acetylene from carbon dioxide and ethylene is challenging in view of their similar sizes and physical properties. Metal–organic frameworks (MOFs) in general are strong candidates for these separations owing to the presence of functional pore surfaces that can selectively capture a specific target molecule. Here, we report a novel 3D microporous cationic framework named JCM‐1 . This structure possesses imidazolium functional groups on the pore surfaces and pyrazolate as a metal binding group, which is well known to form strong metal‐to‐ligand bonds. The selective sorption of acetylene over carbon dioxide and ethylene in JCM‐1 was successfully demonstrated by equilibrium gas adsorption analysis as well as dynamic breakthrough measurement. Furthermore, its excellent hydrolytic stability makes the separation processes highly recyclable without a substantial loss in acetylene uptake capacity. 相似文献
995.
Inside Cover: Selective Solid–Liquid and Liquid–Liquid Extraction of Lithium Chloride Using Strapped Calix[4]pyrroles (Angew. Chem. Int. Ed. 37/2018)
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996.
Reductive Carbocyclization of Homoallylic Alcohols to syn‐Cyclobutanes by a Boron‐Catalyzed Dual Ring‐Closing Pathway
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Dr. Chinmoy Kumar Hazra Jinhoon Jeong Hyunjoong Kim Prof. Dr. Mu‐Hyun Baik Dr. Sehoon Park Prof. Dr. Sukbok Chang 《Angewandte Chemie (International ed. in English)》2018,57(10):2692-2696
The organoborane‐catalyzed reductive carbocyclization of homoallylic alcohols has been developed by using hydrosilanes as reducing reagents to provide a range of 1,2‐disubstituted arylcyclobutanes. The reaction proceeds in a cis‐selective manner with high efficiency under mild conditions. Mechanistic studies, including deuterium scrambling and Hammett studies, and DFT calculations, suggest a dual ring‐closing pathway. 相似文献
997.
Nana Kwabena Adomako Jeoung Han Kim Yong Taek Hyun 《Journal of Thermal Analysis and Calorimetry》2018,133(1):13-26
The high-temperature oxidation behaviour of CoCrNi, CoCrNiMn, and CoCrNiMnFe equimolar alloys was investigated. All three alloys have a single-phase face-centred cubic structure. Thermogravimetric analyses (TGA) were conducted at temperatures ranging from 800 to 1000 °C for 24 h in dry air. The kinetic curves of the oxidation were measured by TGA, and the microstructure and chemical element distribution in different regions of the specimens were analysed. The oxidation kinetics of the three alloys followed the two-stage parabolic rate law, with rate constants generally increasing with increasing temperature. CoCrNi displayed the highest resistance to oxidation, followed by CoCrNiMnFe and CoCrNiMn exhibiting the least resistance to oxidation. The addition of Mn to CoCrNi increased the oxidation rate. The oxidation resistance of CoCrNiMn was enhanced by the addition of Fe. Less Mn Content and the formation of more Cr2O3 were responsible for the reduction in the oxidation rates of CoCrNiMnFe. The calculated activation energies of CoCrNiMn and CoCrNiMnFe at 800, 850 and 900 °C were 108 and 137 kJ mol?1, respectively, and are comparable to that of Mn diffusion in Mn oxides. The diffusion of Mn through the oxides at 800–900 °C is considered to be the rate-limiting process. The intense diffusion of Cr at 1000 °C contributed to the formation of CrMn1.5O4 spinel with Mn in the outer layer of CoCrNiMn and Cr2O3 in the outer layer of CoCrNiMn. 相似文献
998.
An efficient and benign method for the preparation of aminomethyl-substituted fullerenes has been developed. The process, involving catalyst free, visible-light irradiation of 10% EtOH-toluene solutions containing fullerene C60 and N-trimethylsilylmethyl-substituted amines by using a 20 W compact fluorescent lamp, leads to formation of aminomethyl-substituted fullerene adducts in a highly efficient manner. The photoaddition reaction takes place via a pathway initiated by visible light absorption by C60, followed by SET from the amine to the triplet excited state of C60. Ethanol-promoted desilylation of the resulting a minimum radical then generates the corresponding α-amino radical which couples with the C60 radical anion to form the anion precursor of the fullerene adducts. The new approach using visible-light takes place under mild conditions and it does not require the use of photocatalysts. Thus, the method developed in this effort could broadens the range of functionalized fullerene derivatives that can be readily prepared. 相似文献
999.
Haseo Ki 《Transactions of the American Mathematical Society》1997,349(7):2845-2870
We show that the Denjoy rank and the Zalcwasser rank are incomparable. We construct for any countable ordinal differentiable functions and such that the Zalcwasser rank and the Kechris-Woodin rank of are but the Denjoy rank of is 2 and the Denjoy rank and the Kechris-Woodin rank of are but the Zalcwasser rank of is 1. We then derive a theorem that shows the surprising behavior of the Denjoy rank, the Kechris-Woodin rank and the Zalcwasser rank.
1000.