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81.
Dikarev EV Shpanchenko RV Andreini KW Block E Jin J Petrukhina MA 《Inorganic chemistry》2004,43(18):5558-5563
The crystal structure of a new hybrid product comprised of two rigid building blocks, namely dirhodium(II) tetraacetate, [Rh(2)(O(2)CCH(3))(4)] (1), and 2,6-diselenaspiro[3.3]heptane, Se(2)C(5)H(8) (2), has been solved ab initio using laboratory source X-ray powder diffraction (XRPD) data. The rigid body refinement approach has been applied to assist in finding an adequate model and to reduce the number of the refined parameters. Complex [Rh(2)(O(2)CCH(3))(4).mu(2)-Se(2)C(5)H(8)-Se,Se'] (3) conforms to the triclinic unit cell with lattice parameters of a = 8.1357(4), b = 8.7736(4), and c = 15.2183(8) A, alpha = 77.417(3), beta = 88.837(3), and gamma = 69.276(4) degrees, V = 989.66(8) A(3), and Z = 2. The centrosymmetric P space group was selected for calculations. The final values of the reduced wR(p), R(p), and chi(2) were calculated at 0.0579, 0.0433, and 5.95, respectively. The structure of 3 is a one-dimensional zigzag polymer built on axial Rh...Se interactions at 2.632(6) A. The 2,6-diselenaspiro[3.3]heptane ligand acts as a bidentate linker bridging dirhodium units via both selenium atoms. The geometrical parameters of individual groups for rigid body refinement have been obtained from X-ray powder data for dirhodium(II) tetraacetate (1) and from single-crystal X-ray diffraction for diselenium molecule 2. The crystal structures of 1 and 2 are reported here for the first time. For 1 indexing based on XRPD data has resulted in the triclinic unit cell P with lattice parameters of a = 8.3392(7), b = 5.2216(5), and c = 7.5264(6) A, alpha = 95.547(10), beta = 78.101(6), and gamma = 104.714(13) degrees, V = 309.51(5) A(3), and Z = 1. The final values were wR(p) = 0.0452, R(p) = 0.0340, and chi(2) = 1.99. The 1D polymeric motif built on axial Rh.O interactions of the centrosymmetric dirhodium units has been confirmed for the solid-state structure of 1. Compound 2,6-diselenaspiro[3.3]heptane (2) conforms to the monoclinic space group P2(1)/c with the unit cell parameters of a = 5.9123(4), b = 19.6400(13), and c = 5.8877(4) A, beta = 108.5500(10) degrees, V = 648.15(8) A(3), and Z = 4. 相似文献
82.
[reaction: see text] Chloromethanesulfonylethene (3a) and dichloromethanesulfonylethene (3b) were prepared by oxidation of the adducts of ethylene and ClCH(2)SCl or Cl(2)CHSCl, respectively, followed by NaHCO(3) dehydrochlorination. With dienes, 3a gave Diels-Alder adducts that, with base, underwent Ramberg-B?cklund reaction, giving products corresponding to the adducts of the dienes and allene. Similarly, 3b gave Diels-Alder adducts that, with base in the presence of the novel chlorine source MeSO(2)CCl(3), cleanly afforded products corresponding to the adducts of the dienes and 1,1-dichloropropa-1,2-diene. 相似文献
83.
Increasing speciation demands in clinical chemistry, toxicology and nutrition have made the determination of the total elements in a sample inadequate; the amount of an element and the chemical forms in which it is present need to be known. Inductively coupled plasma mass spectrometry (ICP-MS) was used after high-performance liquid chromatographic (HPLC) separation, as was electrospray ionization mass spectrometry (ESI-MS). The effect of variation of the number of carbon atoms in perfluorinated carboxylic acids used as ion-pairing agents for the separation of selenium compounds was examined. Trifluoroacetic acid (0.1%), pentafluoropropanoic acid (0.1%) or heptafluorobutanoic acid (0.1%; HFBA) were alternatively used as additives to methanol-water (1:99, v/v) solutions as mobile phases. Reversed-phase HPLC-ICP-MS with 0.1% HFBA in the mobile phase allowed more than 20 selenium compounds to be separated in 70 min in an isocratic elution mode; the separation of natural selenium-enriched sample extracts was examined and explained. The pH of the 0.1% HFBA solution was modified with hydrochloric acid or ammonia and the pH of the sample extracts before injection was modified in order to overcome unwanted double peak formation in the chromatograms of sample extracts. Oxidations of standard gamma-glutamyl-Se-methylselenocysteine and Se-methylselenocysteine were carried out using 30% H2O2 solution and identifications of selenium-containing oxidation products were made using HPLC-ICP-MS and HPLC-ESI-MS. The principal organic oxidation product in both cases was methaneseleninic acid (MeSeO2H). 相似文献
84.
Fluorodesilylation of trimethylsilylmethanesulfinyl chloride 4 in the presence of cyclopentadiene gives 2-thiabicyclo[2.2.1]hept-5-ene endo-2-oxide,5; in a like manner 1-trimethylsilylalkanesulfonic anhydrides afford endo- and exo-3-alkyl-2-thiabicyclo[2.2.1]hept-5-ene 2,2-dioxides, with the endo isomer predominating. Sulfine and alkyl sulfenes are invoked. 相似文献
85.
86.
A. H. Garde Åse Marie Hansen Thomas Block Nikolajsen 《Accreditation and quality assurance》2003,8(1):16-20
An inter-laboratory comparison study for cortisol in saliva is reported in the present study. Nine laboratories representing
four different methods participated in the study. Each laboratory measured five blind samples prepared from natural saliva
spiked with a pure certified reference material in the range 0–70 nmol/L. The average observed values were established as
means of eight laboratories, because one laboratory was excluded as an outlier. The natural content of cortisol in the pooled
saliva was 6.8 nmol/L. The recovery of the certified reference material was 83%–131% (164% for the outlying laboratory). For
five laboratories the 95%-confidence intervals of the recoveries did not cover 100%. The standard deviations for a concentration
of 10 nmol/L were estimated for each laboratory. They were 0.64–1.67 nmol/L (6.26 nmol/L for the outlying laboratory). The
present study emphasizes the need for an external proficiency-testing scheme and a certified reference material for cortisol
in saliva.
Received: 8 May 2002 Accepted: 3 September 2002 相似文献
87.
Zinc dimethyl-, methylphenyl-, and diphenylphosphinate have been prepared by the reaction of Zn(C2H3O2)2·2H2O with the appropriate acid or salt and found to exist in amorphous and crystalline forms. Zinc methylphenylphosphinate, the most tractable, exhibits many of the physical attributes of polymeric materials, both in solution and bulk form, supporting our earlier suggestion that these compounds are double-bridged coordination polymers. Thermogravimetric analysis indicates initial decomposition temperatures of 440, 425, and 490°C., respectively, for the three polymers, but long-term studies show initiation of decomposition at somewhat lower temperatures. 相似文献
88.
89.
A. Berliner W. H. Westphal J. Errera Fr. L?we P. W. Danckwortt J. Plotnikow W. Block F. Plato K. Jellinek P. Debye E. Schr?dinger E. Lange F. -V. v. Hahn und F. Kuntze 《Fresenius' Journal of Analytical Chemistry》1929,76(7-8):281-284
Ohne Zusammenfassung 相似文献
90.
The aim of this review article is to give an introduction to implementations of the Ising model accelerated by Graphics Processing Units (GPUs) and to summarize different techniques that have been used and tested by different groups. Different parallelization schemes and algorithms are discussed and compared, technical details are pointed out and their performance potential is evaluated. 相似文献