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91.
Normen Peulecke Andreas Ohff Wolfgang Baumann Rhett Kempe Vladimir V. Burlakov Uwe Rosenthal 《Journal of organometallic chemistry》1996,520(1-2):235-239
The reaction of Cp2Zr(L)(η2-Me3SiC2) (L = THF, py) with equimolar amounts of H2C = CMe-CHO at room temperature depends strongly on the ligands L and the solvents that are used. With L = THF, in the THF solution the insertion product 1 was isolated, whereas by conducting the reaction in n-hexane solution an alkyne substitution with 1,4-coordination of the methacrolein takes place and the binuclear complex [ 2 was obtained. In conttrast, with L = py (a stronger ligand) only a 1:1 ratio of 1 and 2 was observed in both THF and in n-hexane. At 50°C complex 1 was converted into 2 and the alkyne was eliminated quantitatively.
Complexes 1 and 2 were characterized by IR and NMR spectroscopical measurements and 1 by an additional X-ray structure determination. 相似文献
92.
Paloma Sevillano Sven Koenig Daniel Himmel Olaf Fuhr Dieter Fenske 《无机化学与普通化学杂志》2005,631(11):2236-2240
The reactions of [Co2(CO)8] with E(SiMe3)2 (E = Se, Te) in CH2Cl2 result in the formation of the compounds [Co4Se2(CO)10]> ( 1 ) and [Co4Te2(CO)11] ( 2 ), respectively. Both cluster complexes have similar molecular structures in which the cobalt atoms form four‐membered rings with μ4‐bridging chalcogen atoms (Se and Te) above and below the plane of the metal atoms and the carbonyl ligands as either terminal or μ2‐bridging ligands. DFT‐calculations for both compounds have been carried out in order to obtain some more information about their electronic distribution. In the presence of the phosphine Ph2PC≡CPPh2 (dppa), the reaction of [Co2(CO)8] with Se(SiMe3)2 leads to the formation of [Co8Se4(CO)16(μ‐dppa)2] ( 3 ). During the reaction two molecules of [Co2(CO)8] have been added to the acetylene groups of the dppa ligands, whilst the remaining cobalt atoms coordinate to the phosphorus atoms of the phosphine. In this compounds the selenium atoms act as μ3‐ligands, bridging the metal atoms bonded to the phosphorus with those bonded to the acetylene groups. 相似文献
93.
Sven Larsson 《Chemical physics letters》1976,40(3):362-366
The ESCA inner shell spectra of Cu compounds are investigated theoretically. It is shown that the large satellites appearing for Cu(II) compounds correspond to shake-up states which are close to the configuration p5d9 and have the characteristic multiplet splitting of this configuration. 相似文献
94.
Pooransingh N Pomerantseva E Ebel M Jantzen S Rehder D Polenova T 《Inorganic chemistry》2003,42(4):1256-1266
A series of 11 oxovanadium(V) complexes mimicking the active site of vanadium haloperoxidases have been investigated by (51)V magic angle spinning NMR spectroscopy and density functional theory (DFT). The MAS spectra are dominated by the anisotropic quadrupolar and chemical shielding interactions; for these compounds, C(Q) ranges from 3 to 8 MHz, and delta(sigma) is in the range 340-730 ppm. The quadrupolar coupling and chemical shielding tensors as well as their relative orientations have been determined by numerical simulations of the spectra. The spectroscopic NMR observables appear to be very sensitive to the details of the electronic and geometric environment of the vanadium center in these complexes. For the four crystallographically characterized compounds from the series, the quadrupolar and chemical shielding anisotropies were computed at the DFT level using two different basis sets, and the calculated tensors were in general agreement with the experimental solid-state NMR data. A combination of (51)V solid-state NMR and computational methods is thus beneficial for investigation of the electrostatic and geometric environment in diamagnetic vanadium systems with moderate quadrupolar anisotropies. 相似文献
95.
96.
Andrzej Chmura Sven Rustler Monica Paravidino Fred van Rantwijk Andreas Stolz Roger A. Sheldon 《Tetrahedron: Asymmetry》2013,24(19):1225-1232
Enantiomerically pure (S)-mandelic acid was synthesised from benzaldehyde by sequential hydrocyanation and hydrolysis in a bienzymatic cascade at starting concentrations up to 0.25 M. A cross-linked enzyme aggregate (CLEA) composed of the (S)-selective oxynitrilase from Manihot esculenta and the non-selective nitrilase from Pseudomonas fluorescens EBC 191 was employed as the biocatalyst. The nitrilase produces approx. equal amounts of (S)-mandelic acid and (S)-mandelic amide from (S)-mandelonitrile under standard conditions, but we surprisingly found that high (up to 0.5 M) concentrations of HCN induced a marked drift towards amide production. By including the amidase from Rhodococcus erythopolis in the CLEA we obtained (S)-mandelic acid as the sole product in 90% yield and >99% enantiomeric purity. 相似文献
97.
98.
99.
Siwei Wang Jesse Ward Sven Leyffer Stefan M. Wild Chris Jacobsen Stefan Vogt 《Journal of synchrotron radiation》2014,21(3):568-579
A novel approach to locate, identify and refine positions and whole areas of cell structures based on elemental contents measured by X‐ray fluorescence microscopy is introduced. It is shown that, by initializing with only a handful of prototypical cell regions, this approach can obtain consistent identification of whole cells, even when cells are overlapping, without training by explicit annotation. It is robust both to different measurements on the same sample and to different initializations. This effort provides a versatile framework to identify targeted cellular structures from datasets too complex for manual analysis, like most X‐ray fluorescence microscopy data. Possible future extensions are also discussed. 相似文献
100.