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排序方式: 共有356条查询结果,搜索用时 265 毫秒
1.
Sharma G. Anthal S. Deshmukh M. B. Mohire P. P. Bhosale T. R. Sudarsanakumar C. Kant R. 《Crystallography Reports》2021,66(7):1233-1237
Crystallography Reports - The structure of 3,3'-[(3-sulfanylphenyl)methylene]bis(4-hydroxy-2H-1-benzopyran-2-one) : 5-methyl-1,3-thiazol-2(3H)-imine was determined by X-ray crystallography. It... 相似文献
2.
Tathe Shraddha V. Deshmukh Prashant R. Kashid Arun M. Gaikwad Shubhangee 《平面色谱法杂志一现代薄层色谱法》2019,32(6):495-500
JPC – Journal of Planar Chromatography – Modern TLC - This paper includes the development of a novel, systematic, quality by design (QbD)-based high-performance thin-layer... 相似文献
3.
4.
Heinz J. Robota Laura A. Richard Soumitra Deshmukh Steve LeViness Daniele Leonarduzzi Diarmid Roberts 《Catalysis Surveys from Asia》2014,18(4):177-182
Each process configuration for practicing the Fischer–Tropsch synthesis places demands particular to that configuration on the catalyst to be used. We discuss how a particular catalyst, prepared by the OMX (organic matrix combustion) method, when used in conjunction with the Velocys microchannel reactor system, results in a very stable, high performance Fischer–Tropsch synthesis system. With the ability to remove heat far more effectively than a conventional reactor system, this microchannel reactor requires a catalyst with much higher volumetric reactive site density. Further, with such a high volumetric reaction rate, mass transfer effects will be important in both the observed activity and selectivity of the operating catalyst. Nevertheless, the catalyst prepared using the OMX method exhibits an apparent turnover frequency which is considerably higher than reported for other catalysts in the literature. In addition to high activity, an economically useful catalyst must exhibit a stable, high selectivity for liquid products and be able to recover near-fresh performance using a regeneration approach which can be carried out with the catalyst in-place. An example of such a stable, multiply regenerated catalyst is given. Finally, further development has focused on a catalyst with even higher C5+ selectivity. 相似文献
5.
Dr. Sumith A. Kularatne Vishal Deshmukh Dr. Marco Gymnopoulos Dr. Sandra L. Biroc Dr. Jinming Xia Shailaja Srinagesh Dr. Ying Sun Dr. Ning Zou Dr. Mark Shimazu Dr. Jason Pinkstaff Dr. Semsi Ensari Nick Knudsen Anthony Manibusan Dr. Jun Y. Axup Dr. Chan Hyuk Kim Prof. Vaughn V. Smider Dr. Tsotne Javahishvili Prof.Dr. Peter G. Schultz 《Angewandte Chemie (International ed. in English)》2013,52(46):12101-12104
6.
Shahaji Gaikwad Satej Deshmukh Samir H. Chikkali 《Journal of polymer science. Part A, Polymer chemistry》2014,52(1):1-6
This overview provides insights into the current state‐of‐the‐art solutions to insertion copolymerization of functional olefinic monomers. The challenges in insertion copolymerization of functional olefinic monomers, with a special emphasis on vinyl halides, are highlighted. The crucial design of the Pd–phosphinesulfonate [Pd(PO)] enables up to 3.6 mol % incorporation of vinyl fluoride (VF) in an ethylene–VF copolymerization reaction. In a significant development, insertion copolymerization of industrially relevant functional olefin, that is, vinyl chloride (VC), was unambiguously ascertained, and a detectable amount of VC (0.4 mol %) was incorporated (at the chain end). In a detailed investigation, the in situ existence of (PO)Pd? H species during the polymerization was revealed, and it was demonstrated that these are indeed responsible for VC incorporation. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1–6 相似文献
7.
Jorna Kalim Thibaut Duhail Dr. Ewa Pietrasiak Dr. Elsa Anselmi Dr. Emmanuel Magnier Prof. Dr. Antonio Togni 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(8):2638-2642
The direct trifluoromethylation of a variety of aliphatic alcohols using a hypervalent iodosulfoximine reagent afforded the corresponding ethers in moderate to good yields (14–72 %). Primary, secondary, and even tertiary alcohols, including examples derived from natural products, underwent this transformation in the presence of catalytic amounts of zinc bis(triflimide). Typical reaction conditions involved a neat mixture of 6.0 equivalents of the alcohol with 1.0 equivalent of the reagent, with the majority of reactions complete within 2 h with 2.5 mol % of the Lewis acid catalyst. Furthermore, experimental evidence was provided that the C−O bond-forming process occurred via the coordination of the alcohol to the iodine atom and subsequent reductive elimination. 相似文献
8.
Sharvari Deshmukh Kalyani Kamde Arun Jana Sanjivani Korde Rajib Bandyopadhyay Ravi Sankar Nabarun Bhattacharyya R.A. Pandey 《Analytica chimica acta》2014
Electronic nose systems when deployed in network mesh can effectively provide a low budget and onsite solution for the industrial obnoxious gaseous measurement. For accurate and identical prediction capability by all the electronic nose systems, a reliable calibration transfer model needs to be implemented in order to overcome the inherent sensor array variability. In this work, robust regression (RR) is used for calibration transfer between two electronic nose systems using a Box–Behnken (BB) design. Out of the two electronic nose systems, one was trained using industrial gas samples by four artificial neural network models, for the measurement of obnoxious odours emitted from pulp and paper industries. The emissions constitute mainly of hydrogen sulphide (H2S), methyl mercaptan (MM), dimethyl sulphide (DMS) and dimethyl disulphide (DMDS) in different proportions. A Box–Behnken design consisting of 27 experiment sets based on synthetic gas combinations of H2S, MM, DMS and DMDS, were conducted for calibration transfer between two identical electronic nose systems. Identical sensors on both the systems were mapped and the prediction models developed using ANN were then transferred to the second system using BB–RR methodology. The results showed successful transmission of prediction models developed for one system to other system, with the mean absolute error between the actual and predicted concentration of analytes in mg L−1 after calibration transfer (on second system) being 0.076, 0.1801, 0.0329, 0.427 for DMS, DMDS, MM, H2S respectively. 相似文献
9.
Sandeep G. Yenchalwar Rami Reddy Devarapalli Ashvini B. Deshmukh Dr. Manjusha V. Shelke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(24):7402-7409
The visible‐light response of Au nanoparticles (AuNPs) assembled on rGO through different molecular bridges was investigated by transient photocurrent generation. We prepared rGO with two self‐assembled monolayers (SAMs), one linear and the other with aromatic triazoles through a click cycloaddition reaction. A fivefold photocurrent enhancement was observed for triazole linkers over the aminopropyltrimethoxysilane (APTMS) linker. Cyclic voltammetry (CV) and impedance measurements also suggest fast electron transfer on account of the low resistance offered by the click‐modified rGO surface whereby introduction of triazoles offers the efficient bridge between the donor AuNPs and acceptor rGO. 相似文献
10.
Ziyauddin S. Qureshi Krishna M. Deshmukh Sachin R. Jagtap Nitin S. Nandurkar Bhalchandra M. Bhanage 《Ultrasonics sonochemistry》2009,16(3):308-311
A simple and convenient methodology for selective sulfonation of aromatic compounds using sulfuric acid under sonication is described. The present methodology shows a considerable enhancement in the reaction rate along with improved selectivity compared with the reactions performed under silent conditions. The effect of various parameters such as agitation speed, sulfuric acid concentration, and temperature on reaction system have been investigated and are explained on the basis of ultrasonically generated cavitational effects. 相似文献