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排序方式: 共有2240条查询结果,搜索用时 31 毫秒
1.
Christopher Lombardi Dr. Richard P. Rucker Dr. Robert D. J. Froese Dr. Sepideh Sharif Prof. Pier Alexandre Champagne Prof. Michael G. Organ 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(62):14223-14229
The relative rates of arylation of primary alkylamines with different Pd-NHC catalysts have been measured, as have the relative rates of arylation of the secondary aniline product in an attempt to understand the key ligand design features necessary to have high selectivity for the monoarylated amine product. As the substituents on the N-aryl ring of the NHC increase in size, selectivity for monoarylation increases and this is further enhanced by chlorinating the back of the NHC ring. Computations have been performed on the catalytic cycle of this transformation in order to understand the selectivity obtained with the different catalysts. 相似文献
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Queueing Systems - We consider strategic arrivals to a FCFS service system that starts service at a fixed time and has to serve a fixed number of customers, for example, an airplane boarding... 相似文献
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João M. J. M. Ravasco Dr. Hélio Faustino Dr. Alexandre Trindade Prof. Pedro M. P. Gois 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(1):43-59
Maleimide chemistry stands out in the bioconjugation toolbox by virtue of its synthetic accessibility, excellent reactivity, and practicability. The second-generation of clinically approved antibody–drug conjugates (ADC) and much of the current ADC pipeline in clinical trials contain the maleimide linkage. However, thiosuccinimide linkages are now known to be less robust than once thought, and ergo, are correlated with suboptimal pharmacodynamics, pharmacokinetics, and safety profiles in some ADC constructs. Rational design of novel generations of maleimides and maleimide-type reagents have been reported to address the shortcomings of classical maleimides, allowing for the formation of robust bioconjugate linkages. This review highlights the main strategies for rational reagent design that have allowed irreversible bioconjugations in cysteines, reversible labelling strategies and disulfide re-bridging. 相似文献
4.
Quemet Alexandre Buravand Emilie Peres Jean-Gabriel Dalier Vincent Bejaoui Syriac 《Journal of Radioanalytical and Nuclear Chemistry》2022,331(2):1051-1061
Journal of Radioanalytical and Nuclear Chemistry - This paper details the different steps for the isotopic determination of UAmO2 discs from analytical irradiation. MARIOS and DIAMINO irradiations... 相似文献
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Lana K. Hiscock Brooke M. Raycraft Monika Wałęsa-Chorab Coralie Cambe Alexandre Malinge Prof. Dr. W. G. Skene Hi Taing Prof. Dr. S. Holger Eichhorn Prof. Dr. Louise N. Dawe Prof. Dr. Kenneth E. Maly 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(4):1018-1028
A series of new tetrakis(dialkoxyphenyl) dicyanotetraoxapentacene derivatives ( 1 a – c ) were prepared by reaction of the appropriate terphenyl diols with tetrafluoroterephthalonitrile in good yields. Compounds 1 b and 1 c , which bear hexyloxy and decyloxy side chains, exhibited columnar hexagonal mesophases, as shown by polarized optical microscopy, variable-temperature powder X-ray diffraction, and differential scanning calorimetry. Single-crystal X-ray diffraction of methoxy-substituted 1 a revealed that the dicyanotetraoxapentacene core is highly planar, consistent with the notion that these molecules are able to stack in columnar mesophases. A detailed photophysical characterization showed that these compounds exhibit aggregation-induced emission in solution, emission in nonpolar solvents, weak emission in polar solvents, and strong emission in the solid state both as powder and in thin films. These observations are consistent with a weakly emissive charge-transfer state in polar solvents and a more highly emissive locally excited state in nonpolar solvents. 相似文献
6.
Large‐Scale Synthesis of Enantiopure Molecular Cages: Chiroptical and Recognition Properties 下载免费PDF全文
Sara Lefevre Dawei Zhang Estelle Godart Marion Jean Dr. Nicolas Vanthuyne Jean‐Christophe Mulatier Dr. Jean‐Pierre Dutasta Dr. Laure Guy Prof. Alexandre Martinez 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):2068-2074
A convenient and efficient gram‐scale synthesis for enantiopure hemicryptophane–tren (tren=tris(2‐aminoethyl)amine) derivatives has been developed. The four‐step synthesis is based on the optical resolution of a key intermediate, cyclotriveratrylene, for which the energy barrier for racemization has been measured to ensure that no racemization occurs during the two last steps of the synthetic pathway. The assignments of the absolute configurations have been performed by electronic circular dichroism and the enantiopurity was determined by NMR spectroscopy in the presence of enantiopure camphor sulfonic acid. To highlight the interest of such compounds, the recognition of norephedrine neurotransmitter was investigated and showed a remarkable enantioselectivity towards the C3 symmetrical hosts. Finally, this highly modular synthetic pathway was used to provide eight enantiopure hemicryptophanes with different sizes, shapes, and functionalities. These results underline the high potential of this approach, which could lead to many applications in chiral recognition or asymmetric supramolecular catalysis. 相似文献
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Back Cover: Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement (Chem. Eur. J. 31/2016) 下载免费PDF全文