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201.
Sensitized photo-oxidation of methylcyclohexane as a thin film on seawater by irradiation with natural sunlight 总被引:1,自引:0,他引:1
Methylcyclohexane dissolved in and forming a thin film on purified seawater with traces of anthraquinone added as triplet sensitizer was exposed to natural sunlight in a quartz flask. The water was circulated through a glass cartridge filled with Amberlite XAD-2 for the concentration of reaction products which were identified by GC/MS after elution and silica gel chromatography. They included isomeric methylcyclohexanols as the principal components, primary hydroperoxides, a tentatively identified secondary peroxide, methylcyclohexanones, and acyclic ketones. Mass spectra and mechanisms are discussed as well as possible biological consequences of the formation of these compounds. 相似文献
202.
R. S. A. de Lange K. -N. P. Kumar J. H. A. Hekkink G. M. H. van de Velde K. Keizer A. J. Burggraaf W. H. Dokter H. F. van Garderen T. P. M. Beelen 《Journal of Sol-Gel Science and Technology》1994,2(1-3):489-495
Microporous SiO2 and SiO2/MO2 (M=Ti, Zr, Al; 10 mol% MOx) materials for gas separation membrane applications have been prepared from polymeric sols. Characterization of these sols with SAXS showed that the mean fractal dimension of the SiO2 sols is 1.3–1.4 with a radius of gyration of approximately 2.5 nm. The dried and calcined films are microporous and the pore size distribution was bimodal with maxima at diameters of 0.5 nm and 0.75 nm. For the SiO2/TiO2, SiO2/ZrO2 and SiO2/Al2O3 systems, much milder reaction conditions proved to be necessary to obtain sols with comparable fractal dimensions due to the high reactivity of the Ti/Zr/Al-alkoxides. Microporous supported membranes with molecular sieve-like gas transport properties can be prepared from a relatively wide range of sol structures: from polymers too small to characterize with SAXS to structures with fractal dimensions: 1<d
f<2.04. 相似文献
203.
We report laser photoelectron spectra of the doubly negatively charged fullerenes C(76) (2-), C(78) (2-), and C(84) (2-) at 2.33, 3.49, and 4.66 eV photon energy. From these spectra, second electron affinities and vertical detachment energies, as well as estimates for the repulsive Coulomb barriers are obtained. These results are discussed in the context of electrostatic models. They reveal that fullerenes are similar to conducting spheres, with electronic properties scaling with their size. The experimental spectra are compared with the accessible excited states of the respective singly charged product ions calculated in the framework of time dependent density functional theory. 相似文献
204.
Brigitte Sarry und Arno Lange 《Fresenius' Journal of Analytical Chemistry》1968,241(3):186-196
Zusammenfassung Die optimalen Bedingungen für die photometrische Bestimmung von Tantal mit Pyrogallol in schwefelsaurer Lösung bei 405 nm wurden ausgearbeitet. Das Verfahren wurde statistisch überprüft.
Für die Durchführung der Untersuchungen standen Mittel aus dem ERP-Sondervermögen und dem Fonds der Chemischen Industrie zur Verfügung, für die wir auch an dieser Stelle bestens danken.
Herrn Professor Dr. E. Asmus zum 60. Geburtstag gewidmet. 相似文献
Investigations on the photometric determination of tantalum with pyrogallol
The optimum conditions for the photometric determination of tantalum with pyrogallol in sulphuric acid solution at 405 nm have been elaborated. The method has been checked statistically.
Für die Durchführung der Untersuchungen standen Mittel aus dem ERP-Sondervermögen und dem Fonds der Chemischen Industrie zur Verfügung, für die wir auch an dieser Stelle bestens danken.
Herrn Professor Dr. E. Asmus zum 60. Geburtstag gewidmet. 相似文献
205.
Boesten WH Seerden JP de Lange B Dielemans HJ Elsenberg HL Kaptein B Moody HM Kellogg RM Broxterman QB 《Organic letters》2001,3(8):1121-1124
[reaction: see text]. Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are reported. The Strecker reaction is accompanied by an in situ crystallization-induced asymmetric transformation, whereby one diastereomer selectively precipitates and can be isolated in 76-93% yield and dr > 99/1. The diastereomerically pure alpha-amino nitrile obtained from pivaldehyde (R1 = t-Bu, R2 = H) was converted in three steps to (S)-tert-leucine in 73% yield and >98% ee. 相似文献
206.
A simple and precise method was developed for the analytical and preparative reversed-phase HPLC separation of a mixture of epimeric pavine N-oxides containing 49.1% of (−)-thalimonine N-oxide A and 50.1% of (−)-thalimonine N-oxide B isolated from Thalictrum simplex L. (Ranunculaceae). A reversed-phase system with Nucleosil C18 analytical and preparative columns and ethanol-1.5% aqueous orthophosphoric acid (15:85) as the mobile phase was used. The epimeric pavine N-oxides were completely separated within 50 min. 相似文献
207.
Haplotype studies support slippage as the mechanism of germline mutations in short tandem repeats 总被引:1,自引:0,他引:1
Klintschar M Dauber EM Ricci U Cerri N Immel UD Kleiber M Mayr WR 《Electrophoresis》2004,25(20):3344-3348
Germline mutations of human short tandem repeat (STR) loci are expansions or contractions of repeat arrays which are not well understood in terms of the mechanism(s) underlying such mutations. Although polymerase slippage is generally accepted as a mechanism capable to explain most features of such mutations, it is still possible that unequal crossing over plays some role in those events, as most studies in humans could not exclude unequal crossing over (UCO). Crossing over can be studied by analyzing haplotypes using flanking markers. To check for UCO in mutations, we have analyzed 150 paternity cases for which more than the usual trio (mother, child, and father) were available for testing by analyzing 16 STR loci. In a total of 4900 parent-child allele transfers four mutations were observed at different loci (D8S1179, D18S51, D21S11, and SE33/ACTBP2). To identify the mutated allele and to check for UCO, we typed at least four informative loci flanking the mutated locus and used the pedigree data to establish haplotypes. By doing so we were able to exclude UCO in each case. Moreover, we were able to identify the mutations as one-repeat contractions/expansions. Our data thus support slippage as the mechanism of germline mutations in STRs. 相似文献
208.
209.
Andrea Schfer Berthold Fischer Henning Paul Ren Bosshard Manfred Hesse Max Viscontinif 《Helvetica chimica acta》1992,75(6):1955-1964
This paper marks the first reported detection of radical cations by Electrospray-Ionization Mass Spectrometry (ESI-MS). Electron Spin Resonance (ESR) measurements have proven that the detected radical cation existed already in solution and has not been generated by the electrospray ionization technique. However, we observed that the radical cation can be generated by changes in the ionization conditions. A molar mixture of 2-amino-5,6,7,8-tetrahydro-5-methylpterin-4(4H)-one dihydrochloride ( = 5,6,7,8-tetrahydro-N(5)-methylpterin-2 HCl, N(5)-MTHP-2 HCl), and tris(pentane-2,4-dionato)iron(III) in MeCN at pH 2–3 leads to the formation of a [bis(pentane-2,4-dionato)(2-amino-5,6,7,8-tetrahydro-5-methylpteridin-4 (4H)-one)]iron complex ( = [bis(pentane-2,4-dionato) (5,6,7,8-tetrahydro-N(5)-methylpteridin)]iron complex) which can be detected by ESI-MS. The results suggest that this complex might be an FeII radical cation, which could possibly be a suitable model complex for the active center of the phenylalanine hydroxylase. In the same solution, the stable radical cation of N(5)-MTHP is identified by ESI-MS and ESR. 相似文献
210.
Flow vacuum thermolysis (FVT) of thiophene-2,3-dicarboxylic anhydride () in the presence of 2,3-dimethylbutadiene () gives, in addition to 5,6-dimethylthianaphthene (). small quantities of a dihydrodimethylthianaphthene () and another dimethylthianaphthene () which is probably also formed by dehydrogenation of with chloranil. The partial structures of these minor products are consistent with their being formed by a [2+2]-cycloaddition between and an intermediate aryne, 2,3-didehydrothiophene (), followed by a rearrangement of the resulting adduct and dehydrogenation. FVT of in the presence of 2,5- () or 3,4-dimethylthiophene () also gave a mixture of the dimethylthianaphthenes (, ) which can be rationalized as arising by a [4+2]- and two [2+2]-cycloadditions of the aryne to the thiophenes with subsequent desulfurization. The lack of equilibration of the products , and , was demonstrated and their origin as a function of the structure and reactivity of the aryne discussed. 相似文献