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941.
A series of group 4 metal complexes Zr-(1)(2), Zr-(2)(2), Zr-(3)(2), Zr-(4)(2), Zr-(5)(2), Hf-(1)(2), and Hf-(4)(2) containing two bridged bis(phenolate) ligands of the (OSSO)-type were prepared by the reaction of the corresponding bis(phenol) and group 4 metal precursor MX(4) (X = O(i)Pr, CH(2)Ph) and isolated as robust, colorless crystals. NMR spectra indicate D(2) symmetry, in agreement with the solid state structure determined by single crystal X-ray diffraction study of the complexes Zr-(1)(2), Hf-(1)(2), Zr-(3)(2), Zr-(4)(2), and Zr-(5)(2). The complexes with the 1,4-dithiabutanediyl bridged ligands exhibit a highly symmetric coordination around the metal center. The introduction of the rigid trans-1,2-cyclohexanediyl bridged ligands led to a distorted coordination around the metal center in Zr-(4)(2) and Zr-(5)(2) when the ortho substituent is tert-butyl and the para substituent is larger than methyl. The complexes Zr-(1)(2), Zr-(2)(2), Zr-(3)(2), Zr-(4)(2) as well as Hf-(1)(2) and Hf-(4)(2) initiated the ring-opening polymerization of meso-lactide at 100 °C to give heterotactic polylactide with pronounced heterotacticity (>70%) and varying polydispersity (1.05 < M(w)/M(n) < 1.61). As shown by kinetic studies, zirconium complex Zr-(1)(2) polymerized meso-lactide faster than the homologous hafnium complex Hf-(1)(2). 相似文献
942.
943.
Fingerhut BP Oesterling S Haiser K Heil K Glas A Schreier WJ Zinth W Carell T de Vivie-Riedle R 《The Journal of chemical physics》2012,136(20):204307
Non-adiabatic on-the-fly molecular dynamics (NA-O-MD) simulations require the electronic wavefunction, energy gradients, and derivative coupling vectors in every timestep. Thus, they are commonly restricted to the excited state dynamics of molecules with up to ≈20 atoms. We discuss an approximation that combines the ONIOM(QM:QM) method with NA-O-MD simulations to allow calculations for larger molecules. As a proof of principle we present the excited state dynamics of a (6-4)-lesion containing dinucleotide (63 atoms), and especially the importance to include the confinement effects of the DNA backbone. The method is able to include electron correlation on a high level of theory and offers an attractive alternative to QM:MM approaches for moderate sized systems with unknown force fields. 相似文献
944.
I Matanović JL Belof B Space K Sillar J Sauer J Eckert Z Bačić 《The Journal of chemical physics》2012,137(1):014701
We report rigorous quantum five-dimensional (5D) calculations of the coupled translation-rotation (T-R) eigenstates of a H(2) molecule adsorbed in metal organic framework-5 (MOF-5), a prototypical nanoporous material, which was treated as rigid. The anisotropic interactions between H(2) and MOF-5 were represented by the analytical 5D intermolecular potential energy surface (PES) used previously in the simulations of the thermodynamics of hydrogen sorption in this system [Belof et al., J. Phys. Chem. C 113, 9316 (2009)]. The global and local minima on this 5D PES correspond to all of the known binding sites of H(2) in MOF-5, three of which, α-, β-, and γ-sites are located on the inorganic cluster node of the framework, while two of them, the δ- and ε-sites, are on the phenylene link. In addition, 2D rotational PESs were calculated ab initio for each of these binding sites, keeping the center of mass of H(2) fixed at the respective equilibrium geometries; purely rotational energy levels of H(2) on these 2D PESs were computed by means of quantum 2D calculations. On the 5D PES, the three adjacent γ-sites lie just 1.1 meV above the minimum-energy α-site, and are separated from it by a very low barrier. These features allow extensive wave function delocalization of even the lowest translationally excited T-R eigenstates over the α- and γ-sites, presenting significant challenges for both the quantum bound-state calculations and the analysis of the results. Detailed comparison is made with the available experimental data. 相似文献
945.
We simulate the interchain polaron recombination process in conjugated polymer systems using a nonadiabatic molecular dynamics method, which allows for the coupled evolution of the nuclear degrees of freedom and multiconfigurational electronic wavefunctions. Within the method, the appropriate spin symmetry of the electronic wavefunction is taken into account, thus allowing us to distinguish between singlet and triplet excited states. It is found that the incident polarons can form an exciton, form a bound interchain polaron pair, or pass each other, depending on the interchain interaction strength and the strength of an external electric field. Most importantly, we found that the formation of singlet excitons is considerably easier than triplet excitons. This shows that in real organic light emitting devices, the electroluminescence quantum efficiency can exceed the statistical limitation value of 25%, in agreement with experiments. 相似文献
946.
Almeida C Hemberger Y Schmitt SM Bouhired S Natesan L Kehraus S Dimas K Gütschow M Bringmann G König GM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(28):8827-8834
A marine-derived fungus of the genus Stachylidium was isolated from the sponge Callyspongia cf. C. flammea. Chemical investigation of the bioactive fungal extract led to the isolation of the novel phthalimidine derivatives marilines A(1) (1a), A(2) (1b), B (2), and C (3). The absolute configurations of the enantiomeric compounds 1a and 1b were assigned by a combination of experimental circular dichroism (CD) investigations and quantum chemical CD calculations. The skeleton of marilines is most unusual, and its biosynthesis is suggested to require uncommon biochemical reactions in fungal secondary metabolism. Both enantiomers, marilines A(1) (1a) and A(2) (1b), inhibited human leukocyte elastase (HLE) with an IC(50) value of 0.86 μM. 相似文献
947.
Crispin Amiri Naini Marc Thomas Steffen Franzka Sven Frost Mathias Ulbricht Nils Hartmann 《Macromolecular rapid communications》2013,34(5):417-422
A laser temperature‐jump technique is used to probe the impact of sodium halides on the temperature‐dependent switching kinetics and thermodynamics of poly(N‐isopropylacrylamide) brushes. An analysis on the basis of a two‐state model reveals van't Hoff enthalpy and entropy changes. Sodium halides increase the endothermicity and the entropic gain of the switching process below and above Tc following the Hofmeister series: NaCl > NaBr > NaI. In contrast, enthalpic and entropic changes at Tc remain virtually unaffected. This provides an unprecedented insight into the underlying switching energetics of this classic stimuli‐responsive polymer. Because of its model character, these results represent an essential reference on the way to unpuzzle the molecular driving forces of the Hofmeister effect. 相似文献
948.
The effect of perturbing electric fields and electric-field gradients on the nuclear quadrupole coupling in molecules is investigated. The theory for the first-order effects is developed and it is shown that not only a perturbing field gradient but also a perturbing field, and higher terms, induce a finite field gradient at a nucleus in a molecule. The so-called Sternheimer (anti)shielding is thus considerably more complex in molecular than in atomic systems. The different shielding components have been calculated for HCl, HCN and NH4 + using a finite perturbation ab initio molecular orbital method. The calculated values are then used to rationalize experimentally determined 14N quadrupole coupling constants in condensed media for HCN and NH4 +. 相似文献
949.
Abstract The geometric, electronic, and optical properties of poly-[3-(4-octylphenyl)-thiophene] are studied. The effect of the side groups as well as doping is analyzed. Band structures, oscillator strengths and optical absorption spectra are calculated. Absorption spectra reported for the doped polymer show up to four peaks below the band-gap energy. 相似文献
950.
Non-invasive heartbeat sensors to measure the cardiac activity of crustaceans have been adapted for use under hyperbaric conditions. Able to record data continuously over long timescales, these sensors can collect high-resolution data on the physiological state of an organism up to a tested limit of 300 atm. Using this technique, heart rate was recorded in a juvenile of the sublittoral spider crab, Maja brachydactyla (Decapoda: Majidae), when subjected to hydrostatic pressures of 1, 50, 100, and 150 atm for periods of 30 min. Heart rate increases with pressure until 100 atm (one-way repeated measures ANOVA: F (4, 25)=154.76, p<0.001). However, the significant decrease in the mean heart rate from 137.07 bpm at 100 atm to 118.40 bpm at 150 atm (t-test: t=4.581, d.f.=10, p<0.001) indicates a mechanistic limit in the cardiac response of this species to pressures beyond 100 atm. This method could be potentially applied to any marine invertebrate with a neurogenic heart. 相似文献