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991.
Photocatalytic hydrogen production from water solutions of dimethyl methylphosphonate (DMMP), trimethyl phosphate (TMP), triethyl phosphate (TEP), and radiation protective amine WR 2721, that imitate nerve chemical warfare agents was studied for the first time. Platinized titianium dioxide Degussa P25 was used as catalyst. No significant hydrogen evolution was detected without organic electron donors – sacrificial agents. 相似文献
992.
Alexander Gavrilyuk Ulf TritthartWolfgang Gey 《Solar Energy Materials & Solar Cells》2011,95(7):1846-1851
We carried out the experiments which show unambiguously that not one, as it was commonly accepted, but three optical absorption bands corresponding to different color centers arise in the nanosized MoO3 films due to hydrogen atoms. Varying the conditions for the photoinjection of hydrogen into the MoO3 films, it is possible to change drastically the correlation between the concentrations of different arising centers, which in turn yields the great difference in the optical absorption spectra. Our findings are crucial for understanding of the nature of electrochromism and photochromism not only in MoO3 films but also in the series of the transition metal oxide films. 相似文献
993.
Multibody System Dynamics - The structural analysis and optimization of flexible multibody systems become more and more popular due to the ability to efficiently compute gradients using... 相似文献
994.
Reitz Alexander Grydin Olexandr Schaper Mirko 《Metallurgical and Materials Transactions A》2022,53(8):3125-3142
Metallurgical and Materials Transactions A - With an innovative optical characterization method, using high-temperature digital image correlation in combination with thermal imaging, the local... 相似文献
995.
Ali Alipour Najmi Elchin Jafariyeh-Yazdi Mojgan Hadian Jos Hermans Prof. Rainer Bischoff Prof. Jun Yue Prof. Alexander Dömling Prof. Arne Wittstock Dr. Hjalmar P. Permentier 《ChemMedChem》2022,17(11):e202200040
A novel method for the selective catalytic N-dealkylation of drug molecules on a nanoporous gold (NPG) catalyst producing valuable N-dealkylated metabolites and intermediates is described. Drug metabolites are important chemical entities at every stage of drug discovery and development, from exploratory discovery to clinical development, providing the safety profiles and the ADME (adsorption, distribution, metabolism, and elimination) of new drug candidates. Synthesis was carried out in aqueous solution at 80 °C using air (oxygen source) as oxidant, in single step with good isolated yields. Different examples examined in this study showed that aerobic catalytic N-dealkylation of drug molecules on NPG has a broad scope supporting N-deethylation, N-deisopropylation and N-demethylation, converting either 3° amines to 2° amines, or 2° amines to 1° amines. 相似文献
996.
Journal of Materials Science - For decades, a wide variety of products have benefitted from the use of flexible PVC, ranging from healthcare to cable to packaging & household items. The... 相似文献
997.
Rodríguez-Faneca Cristina Maz-Machado Alexander Gutiérrez-Rubio David Pedrosa-Jesús Cristina 《Scientometrics》2022,127(7):4237-4249
Scientometrics - Many international studies have pointed out the under-representation of women on Editorial Boards of both Science and Social Science journals. Their presence as Editorial Board... 相似文献
998.
Tran Thi Ngoc Trang Felfernig Alexander Trattner Christoph Holzinger Andreas 《Journal of Intelligent Information Systems》2021,57(1):171-201
Journal of Intelligent Information Systems - Nowadays, a vast amount of clinical data scattered across different sites on the Internet hinders users from finding helpful information for their... 相似文献
999.
Mireia Casanovas Montasell Anna Baumann Prof. Alexander N. Zelikin 《Chembiochem : a European journal of chemical biology》2023,24(15):e202300304
Activating and masking enzymatic activity on demand is of the highest importance in nature. It is achieved by chemical interconversion of enzymes and the corresponding zymogens through, for example, proteolytic processing or reversible phosphorylation, and affords on-demand activation of enzymes, controlled in space and/or time. In stark contrast, examples of chemical zymogens are very few, and in most cases these are based on disulfide chemistry, which is largely indiscriminate as to the nature of the activating thiol. In this work, we address an outstanding challenge of specificity of reactivation of chemical zymogens. We achieve this through engineering affinity between the chemical zymogen and the activator. Additional, higher-level control over zymogen reactivation is installed in a nature-mimicking approach using steroidal hormones. Taken together, the results of this study take a step towards establishing the specificity of reactivation of synthetic, chemical zymogens. We anticipate that the results of this study will contribute significantly to the development of chemical zymogens as tools for diverse use in chemical biology and biotechnology. 相似文献
1000.
Alexander Pontarelli Prof. Dr. Christopher J. Wilds 《Chembiochem : a European journal of chemical biology》2023,24(9):e202300068
The introduction of chemical modifications on the nucleic acid scaffold has allowed for the progress of antisense oligonucleotides (ASOs) in the clinic for the treatment of a variety of disorders. In contribution to the repertoire of gene-silencing nucleic acid modifications, herein we report the synthesis and incorporation of C5-propynyl arabinouridine ( araUP ) and arabinocytidine ( araCP ) into mixed-base ASOs containing a pyrimidine core. Substitution of the core with araU P and araCP resulted in stabilization of the duplex formed with RNA but not with DNA. Similar results were obtained with ASOs bearing phosphorothioate linkages or methoxyethyl (MOE) wings in a gapmer design. All modified ASOs were compatible with E. coli RNase H mediated degradation of target RNA. Substitution of DNA for araUP and araCP in the central portion of a gapmer with MOE wings demonstrated improved nuclease resistance. These results suggest C5-modified arabinonucleic acids may serve as a potential chemical modification for therapeutic ASOs. 相似文献