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151.
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154.
Stojanović MN Green EG Semova S Nikić DB Landry DW 《Journal of the American Chemical Society》2003,125(20):6085-6089
We report herein a novel system for the parallel processing of molecular recognition events utilizing arrays of oligonucleotide-based fluorescent sensors to characterize hydrophobic molecules in solution. The binding domains of the sensors were based on three-way junctions that utilize double helical stems as framework regions to reliably fold regardless of variations in or around the binding domain. A reporting domain was introduced by the specific substitution of a single phosphodiester group with a phosphorothioate, followed by selective functionalization with a fluorophore. The sensors were organized into cross-reactive arrays to yield characteristic fingerprints for samples containing hydrophobic molecules. The fingerprints can be used to characterize steroids in solution, including complex biologically important fluids. Arrays have the potential for clinical applications such as the detection of gross errors in steroidogenesis. 相似文献
155.
Dragan A. Marković Zoltan Djarmati Ratko M. Jankov Dragan M. Marković Ljubiša M. Ignjatović 《Mikrochimica acta》1996,124(3-4):219-226
The electrochemical behaviour and mechanism of the redox process of the natural antioxidant rosmanol 9-ethyl ether, isolated fromSaliva officinalis L., were studied. The cyclic voltammograms of rosmanol 9-ethyl ether (R9EE), at characteristic pH values, and the electrochemical parameters for all investigated pH values were measured. Three characteristic pH regions, each with different behaviour of R9EE, were identified. In regions of pH < 4 and pH > 5 only one anodic peak appeared, whereas in the solutions of pH 4–5 two anodic peaks could be noted. The overall oxidation mechanism at pH < 4 is an e.H.e.H. oxidation mechanism, which as a final product gives a quinonic molecule. The influence of pH on the second oxidation peak potential tends towards zero in accordance with the preceding dissociation of the one of phenolic groups, thus suggesting an e.e.H. mechanism at pH > 5. This means that at the pH values expected in plant cells, R9EE has an unexpected structure, making this substance a potent antioxidant. Electrochemical and spectrophotometric measurements enabled us to establish an extremely low pK
a value (4.35) for R9EE. 相似文献
156.
Trisubstituted methylalkenes react with methyl sulfite at 25°C in the presence of BF3 · Et2O in the ene-type fashion to give the corresponding methallyl sulfinates. Such compounds can also be prepared under considerably milder conditions by the Et2AlCl-catalyzed reaction of thionyl chloride with mono- and dienes followed by methanolysis of intermediate alkyl sulfinyl chlorides. These reactions represent a new method for terminal functionalization of linear isoprenoids.Deceased Nov.1, 1992.Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 105–107, January, 1993. 相似文献
157.
A. M. Moiseenkov A. V. Lozanova A. A. Surkova V. A. Dragan Yu. A. Strelenko A. V. Buevich 《Russian Chemical Bulletin》1994,43(1):153-160
Electrophilic cyclization of (cyclo)farnesanes containing anexo-methylene group in the a-isoprenoid unit smoothly gives regio- and stereoisomeric octalins subsequently transformed to tricyclic furanosesquiterpenoids related to metabolites of some marine organisms.Deceased.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 156–163, January, 1994.The authors are grateful to the representative of the Bruker company in Moscow, Uve Eichhof, who allowed us to use an AMX-400 spectrometer. 相似文献
158.
Snežana S. Mitić Gordana Ž. Miletić Aleksandra N. Pavlović Snežana B. Tošić Dragan S. Velimirović 《中国化学会会志》2007,54(1):47-54
A kinetic method for the determination of micro quantities of amino acid arginine (Arg) is described in this paper. The catalytic activity of cobalt in the reaction of oxidation of purpurin (1,2,4‐trihydroxy‐antraquinone, PP) by hydrogen peroxide in alkaline buffer solution decreases in the presence of micro quantities of arginine, because of the formation of the complex. Operating conditions for the successful determination of arginine were optimized. The optimized conditions yielded a theoretical detection limit of 1.45 μg mL?1. Kinetic equations are proposed for the investigated process. The interference effects of certain foreign ions and amino acids upon the reaction rate were studied and removed in order to assess the selectivity of the method. The developed procedure was successfully applied to the determination of arginine in various pharmaceutical samples. The typical feature of this procedure is that determination can be carried out at room temperature and in a short analysis time. The newly developed method is simple, inexpensive and efficient for use in the analysis of a large number of samples. 相似文献
159.
By using pH-metric and conductometric methods it has been found that tetracycline (H3TC) forms with WO
4
2–
and MoO
4
2–
ions the following complex compounds: [WO3HTC]2–, [WO3(H2TC)2]2– and [MoO3(H2TC)2]2–. Stability constants log/gb
1
k
=7.86 and log
1
k
=7.80 for [WO3HTC]2– and [MoO3HTC]2–, respectively, have been calculated from pH-metric measurements. 相似文献
160.
Dragan Šepac?eljko Marini? Tomislav PortadaMladen ?ini? Vitomir Šunji? 《Tetrahedron》2003,59(8):1159-1167
Pd(II) complexes of acyclic (1,2;4,5) and macrocyclic (3,6-10) derivatives of 1,5-bis(oxazolines), are tested in the enantioselective allylic alkylation of racemic 1,3-diphenyl-3-acetoxyprop-2-ene (14) by dimethylmalonate anion to allyl malonate derivative 15. Conformation in solution of representative allyl Pd(II) complexes 12 and 13 is studied by 2D NMR and CD spectroscopy. 2D NMR data reveal loss of C2 symmetry of the ligands in Pd(II)allyl-bis(oxazoline) complexes. CD spectra indicate distortion of the bidentate ligand in the complex and a conformationally forced larger twist between two chromophores in the macrocyclic complex. Only moderate variation of enantioselectivity with the length and ring size of the ligand is observed, and a rationale offered. 相似文献