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Albert Strube Gottfried Huttner Jochen Heuser Laszlo Zsolnai 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4)
Abstract Anorganisch-Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 270, D-6900 Heidelberg, F.R.G. 相似文献
966.
967.
Jochen Schröder Fan Wang Eva Ryckeboer Michaël A.F. Roelens 《Optics Communications》2010,283(12):2611-2614
We demonstrate an aberration-free, all-optical, ultra-fast oscilloscope based on the concept of Fourier-transformation with an optical time-lens. By combining the four-wave mixing time-lens with a Fourier-domain optical processor as the dispersive element we avoid aberrations associated with the traditional method of using lengths of fibre for the dispersive elements. We investigate the impact of aberrations due to third-order dispersion and inaccuracies in matching the Fourier-transform condition and demonstrate how these are overcome using the optical processor. The resolution of the oscilloscope is 750 fs. 相似文献
968.
Kastler M Schmidt J Pisula W Sebastiani D Müllen K 《Journal of the American Chemical Society》2006,128(29):9526-9534
Synthetic concepts toward the synthesis of large, not-fully benzenoid polycyclic aromatic hydrocarbons (PAHs), decorated with phase-forming and solubilizing n-dodecyl chains, are presented based on the intramolecular cyclodehydrogenation reaction of suitable oligophenylene precursors. The formal addition of successive C2 units into the armchair bays of the parent hexa-peri-hexabenzocoronene extends the aromatic system and leads to PAHs with a partial zigzag periphery. This variation of the nature of the periphery, symmetry, size, and shape has a distinct impact upon the electronic properties and the organization into columnar superstructures. Both computational and experimental UV/vis spectra, which are in good agreement, emphasize the dependence of the characteristic bands alpha, p, and beta upon the overall size and symmetry of the PAHs. While the number and the substitution patterns of attached n-dodecyl chains do not influence the electronic properties, the thermal behavior and supramolecular organization are strongly influenced, which has been elucidated with differential scanning calorimetry (DSC) and 2D wide-angle X-ray diffractometry (2D-WAXS) on mechanically aligned samples. This study provides valuable insight into the future design of semiconducting materials based on extended PAHs. 相似文献
969.
Chen W Liu F Matsumoto K Autschbach J Le Guennic B Ziegler T Maliarik M Glaser J 《Inorganic chemistry》2006,45(11):4526-4536
The reactions of [Pt(NH3)2(NHCOtBu)2] and TlX3 (X = NO3-, Cl-, CF3CO2-) yielded dinuclear [{Pt(ONO2)(NH3)2(NHCOtBu)}Tl(ONO2)2(MeOH)] (2) and trinuclear complexes [{PtX(RNH2)2(NHCOtBu)2}2Tl]+ [X = NO3- (3), Cl- (5), CF3CO2- (6)], which were spectroscopically and structurally characterized. Strong Pt-Tl interaction in the complexes in solutions was indicated by both 195Pt and 205Tl NMR spectra, which exhibit very large one-bond spin-spin coupling constants between the heteronuclei (1J(PtTl)), 146.8 and 88.84 kHz for 2 and 3, respectively. Both the X-ray photoelectron spectra and the 195Pt chemical shifts reveal that the complexes have Pt centers whose oxidation states are close to that of Pt(III). Characterization of these complexes by X-ray diffraction analysis confirms that the Pt and Tl atoms are held together by very short Pt-Tl bonds and are supported by the bridging amidate ligands. The Pt-Tl bonds are shorter than 2.6 Angstrom, indicating a strong metal-metal attraction between these two metals. Compound 2 was found to activate the C-H bond of acetone to yield a platinum(IV) acetonate complex. This reactivity corresponds to the property of Pt(III) complexes. Density functional theory calculations were able to reproduce the large magnitude of the metal-metal spin-spin coupling constants. The couplings are sensitive to the computational model because of a delicate balance of metal 6s contributions in the frontier orbitals. The computational analysis reveals the role of the axial ligands in the magnitude of the coupling constants. 相似文献
970.
The iron(II) complex of a tetradentate bispidine ligand with two tertiary amines and two pyridine groups (L = dimethyl [3,7-dimethyl-9,9'-dihydroxy-2,4-di-(2-pyridyl)-3,7-diazabicyclo nonan-1,5-dicaboxylate]) is oxidized with tert-butyl hydroperoxide to the corresponding end-on tert-butylperoxo complex [Fe(III)(L)(OOtBu)(X)]n+ (X = solvent, anion). UV-vis, resonance Raman, and EPR spectroscopy, as a function of the solvent, show that this is a spin-crossover compound. The experimentally observed Raman vibrations for both low-spin and high-spin isomers are in good agreement with those computed by DFT. 相似文献