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21.
Peter Šemrl 《Aequationes Mathematicae》1986,31(1):184-190
LetX be a leftA-module, whereA is either a complex Banach *-algebra with an identity element or the field of quaternions. The main result of this note is that forQ, anA-quadratic functional defined onX, there exists a sesquilinear functionalB such thatB(x,x)=Q(x) holds for allxX. 相似文献
22.
J. Mikuski J. Moravec E. Ochab V. Šára 《Journal of Radioanalytical and Nuclear Chemistry》1981,62(1-2):83-90
The structure of the complex Ag·TBDTPP (tetrabutyl S-dithiopyrophosphate) formed in HNO3 medium was studied by IR and NMR methods. The complex is involved in the isomerization of TBDTPP in the presence of Ag+ and NO
3
−
ions. In the IR spectra, we observe the disappearance of P−O−P band and the occurrence of new absorption bands associated
with P−S−P and P=O bonds. The silver ion is coordinated to the thiophosphoryl group of the isomer molecule. The influence
of HNO3 concentration on complex formation is discussed. 相似文献
23.
M. Kabešová I. Vargová T. Šramko J. Gažo 《Journal of Thermal Analysis and Calorimetry》1978,13(1):65-70
The influence of the position of the CH3 group in picoline and lutidine ligands on the degree of chemical change of the NCS groups in coordination compounds of the type Cu(NCS)2L2 (whereL=2-, 3- and 4-picoline, and 2,3-, 2,4-, 2,5-, 2,6-, 3,4- and 3,5-lutidine) is dealt with. The most marked effect of the CH3 group is found to be exerted in position 4. This effect of the methyl group on the degree of chemical change points to the mutual influence of the ligands in coordination compounds of Cu(II).
Zusammenfassung Der Artikel befaßt sich mit dem Einfluß der Lage der CH3 Gruppe in Pikolinen und Lutidinen als Liganden auf den Grad der chemischen Änderungen der Gruppen NSC in Koordinationsverbindungen des Typs Cu(NCS)2L2 (L=2-, 3- und 4-Pikoline, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- und 3,5-Lutidine). Der ausgeprägteste Effekt der CH3 Gruppe wurde in der Position 4 beobachtet. Dieser Einfluß der Methylgruppe auf das Ausmaß der chemischen Änderungen deutet auch auf die gegenseitige Wirkung der Liganden in Koordinationsverbindungen von Cu(II).
Résumé L'article a trait à l'influence de la position du groupe CH2 dans les picolines et lutidines, en tant que ligands, sur le degré des changements chimiques des groupes SCN dans les composés de coordination du type Cu(SCN)2L2 (L=2-, 3 et 4-picoline, 2,3-, 2,4-,2,5-, 2,6-, 3,4- et 3,6-lutidine). L'effet le plus prononcé du groupe CH3 s'observe en position 4. Cette influence du groupe méthyle sur le degré des changements chimiques indique aussi l'influence mutuelle des ligands dans les composés de coordination du Cu(II).
- , , NCS Cu(NCS)2,L2, L=2-, 3- 4- , 2.3-, 2.4-, 2.5-, 2.6-, 3.4- 3.5-. , 4. Cu(II).相似文献
24.
Thermal analysis supported by kinetic calculations was applied exhaustively to these compounds. Under dynamic conditions, tetrafluorometallates(III), which as intermediates, could not be isolated, for the first three compounds. In each case, the final step was the pure metal(III) fluoride. Ammonium hexafluorochromate(III) decomposed directly to the pure chromium(III) fluoride. The decomposition rate of all compounds slowed down towards the end, probably for kinetic reasons. Polymorphic transitions of ammonium hexafluorotitanate(III) were observed at 35 and 100°C. Ammoniumhexafluoroscandate(III) underwent polymorphic transition at 47°C. The decomposition patterns for all these compounds were similar. Conditions for the preparation of pure ammonium tetrafluorometallates(III) of Sc, Ti and V are described. 相似文献
25.
Summary A gas Chromatographic determination of traces of alkali metal O,O-diethyl phosphorodithioates is described. The salts were converted into a volatile derivative by alkylation with diazomethane. The product was identified by gas chromatography-mass spectrometry. With aqueous samples a linear relationship of peak height to amount of salt was obtained in the range 0.04–1 ng and for urine samples a calibration curve was constructed. The detection limit (signal to noise ratio 4/1) was 40 pg of salt. The procedure was successfully used for monitoring phosalone absorption by occupationally exposed persons.
Presented at the Fourth International Congress of Pesticide Chemistry (IUPAC), Zürich, July 24–28, 1978. 相似文献
Zusammenfassung Eine gaschromatographische Bestimmung von Spuren Alkalisalz des Diäthyldithiophosphorsäureesters wurde beschrieben. Die Salze wurden durch Alkylieren mit Diazomethan in ein flüchtiges Derivat übergeführt. Dessen Identifizierung erfolgte mittels eines gaschromatographisch-massenspektrometrischen Systems. In Wasserproben wurde ein lineares Verhältnis der Peakhöhen und der Salzmenge festgestellt und für Urinproben wurde eine Eichkurve ermittelt. Die Nachweisgrenze (Signal zu Rausch 41) wurde bei 40 pg Salz festgestellt. Die Methode wurde für die Kontrolle der Absorption von Phosalon bei beruflich exponierten Personen erfolgreich angewendet.
Presented at the Fourth International Congress of Pesticide Chemistry (IUPAC), Zürich, July 24–28, 1978. 相似文献
26.
Doz. Dr. P. Bukovec B. Orel J. Šiftar 《Monatshefte für Chemie / Chemical Monthly》1974,105(6):1299-1305
The IR- and Raman Spectra of several compounds of the stoichiometryM 2 I M IIIF5H2O and their deuterated analogs have been interpreted on the basis of their crystal structures. The compounds studied were divided into two classes regarding the bonding of water molecules. The main spectroscopic difference between the two classes was found in the region of H2O vibrations in good agreement with theoretical predictions. The metal—fluorine and metal—oxygene vibrations gave no direct information concerning the two types of water. 相似文献
27.
Josef Šlapal 《Aequationes Mathematicae》1995,49(1):115-121
Summary For every ordinaln > 1 we define a categoryT
n
of topological spaces in ech's sense which is isomorphic to a category ofn-ary monorelational systems. We show that every categoryT
n
is an exponential supercategory of the categoryB of finitely generated topological spaces, which means that well-behaved function spacesG
H
can be defined inT
n
wheneverG B. 相似文献
28.
29.
V. Hnatowicz J. Kvítek V. Švorčík V. Rybka V. Popok 《Czechoslovak Journal of Physics》1994,44(6):621-627
Samples of polyethylene (PE) loaded with carbon black up to 8 wt.% and implanted with 150 keV Sb+ ions to the doses from 2×1013–2×1015 cm–2 were studied using standard Rutherford Back Scattering (RBS) technique. On the PE samples implanted to the doses above 2×1014 cm–2, a considerable surface carbonization is observed. The measured parameters of the Sb depth profile are compared with theoretical TRIM estimations. The projected range is by 25% lower than the theoretical one and the range straggling is about twice of that predicted. The differences are explained by stepwise polymer degradation during the ion bombardment. Strong oxidation of the ion implanted polymers is also observed. The oxygen depth profiles from the sample surface up to the depth comparable with Sb+ ion range evolve from nearly uniform one for low ion doses to highly non-uniform one for doses above 1×1015 cm–2. The total oxygen content in the sample surface layer 300 nm thick reaches a maximum for the doses of (1–2)×1014 cm–2.On leave from Belorussian State University, 220050 Minsk, Belarus.The authors thank the member of electrostatic accelerator group at INP for help during RBS measurements. The work was partly (V.H. and J.K.) supported by the Internal Grant Agency of the Academy of Sciences of Czech Republic under the grant No. 14805 and by the Internal Grant Agency of the Ministry of Education of Czech Republic under the grant No. 1002 (V.., V.R., V.H. and J.K.). In the final stage, the work was also supported by the Grant Agency of Czech Republic under the grant No. 202/93/0121. 相似文献
30.
M. Veselský Š. Šáro F. P. Heßberger V. Ninov S. Hofmann D. Ackermann 《Zeitschrift für Physik A Hadrons and Nuclei》1996,356(1):403-410
Velocity distributions and production cross sections of evaporation residues have been measured in the reaction20Ne+208Pb at projectile energies of 8.6, 11.4, 14.9 A.MeV. Essential deviations from statistical model of deexcitation have been
observed. Monte Carlo simulations involving emission of non-equilibrium particles have been used in order to reproduce experimental
velocity, charge and mass distributions of evaporation residues and to estimate indirectly multiplicities of pre-equilibrium
particles.
Communicated by V. Metag 相似文献