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141.
Mitsushiro Nomura Shigemi Kondo Eriko Suzuki Glenn V. Alea Chikako Fujita-Takayama Masatsugu Kajitani 《Journal of organometallic chemistry》2010,695(21):2366-2895
Eight new sulfur-rich [CpCo(dithiolene)] complexes were synthesized from [Zn(dmit)2]2− as a starting material. The structures, electrochemical behavior and electronic absorption spectra of the sulfur-rich [CpCo(S2C2S2Y)] complexes could be compared with the early data of analogous Ni complexes. [CpCo(pddt)] (Y = -(CH2)3-), [CpCo(dpdt)] (Y = -CH2C(CH2)CH2-), [CpCo(bddt)] (Y = -(CH2)4-), [CpCo(dtdt)] (Y = -CH2SCH2-) and [CpCo(poddt)] (Y = -CH2C(O)CH2-) crystallized in all isostructural with the corresponding paramagnetic [CpNi(dithiolene)] complexes, but [CpCo(dmid)] (Y = CO), [CpCo(dddt)] (Y = -(CH2)2-) and [CpCo(F2pddt)] (Y = -CH2CF2CH2-) crystallized in non-isostructural with them. These molecules are associated with intermolecular short S?S contacts in the crystals. [CpCo(F2pddt)] did not show any remarkable S?S contacts but indicated interesting fluorine segregation and Cp?Cp face-to-face interactions. Redox potentials of [CpCo(dithiolene)] complexes were obtained with the cyclic voltammetry measurements and dimerized by electrochemical oxidations. Electronic absorption spectra of [CpCo(dithiolene)] complexes showed visible absorption in the range of 585-701 nm as lowest energy wavelengths (? = 9800-11,800 M−1 cm−1) in solutions, and they were higher energy than those of [CpNi(dithiolene)] complexes (near-IR). 相似文献
142.
A photo-induced radical pair of FADH· and Y8· and in BLUF protein SyPixD was studied by pulsed electron paramagnetic resonance (EPR) spectroscopy. Blue light illumination
at 150 K for 30 min followed by cooling to 50 K during illumination induced the stable radical pair. The EPR signal has been
characterized by a Pake doublet signal with complete S = 1 spin state. The radical pair was utilized as a probe to analyze the oligomer of SyPixD. The relative arrangement of PixD
proteins in the complex was investigated by pulsed electron–electron double resonance (PELDOR) with the orientation selection.
Based on the decameric structure in the crystal, the possible structure for the PELDOR results was discussed. 相似文献
143.
We study the permutation complexity of finite-state stationary stochastic processes based on a duality between values and orderings between values. First, we establish a duality between the set of all words of a fixed length and the set of all permutations of the same length. Second, on this basis, we give an elementary alternative proof of the equality between the permutation entropy rate and the entropy rate for a finite-state stationary stochastic processes first proved in [J.M. Amigó, M.B. Kennel, L. Kocarev, The permutation entropy rate equals the metric entropy rate for ergodic information sources and ergodic dynamical systems, Physica D 210 (2005) 77-95]. Third, we show that further information on the relationship between the structure of values and the structure of orderings for finite-state stationary stochastic processes beyond the entropy rate can be obtained from the established duality. In particular, we prove that the permutation excess entropy is equal to the excess entropy, which is a measure of global correlation present in a stationary stochastic process, for finite-state stationary ergodic Markov processes. 相似文献
144.
Michiro Kondo 《Mathematica Slovaca》2014,64(5):1093-1104
We define states on bounded commutative residuated lattices and consider their property. We show that, for a bounded commutative residuated lattice X,
- If s is a state, then X/ker(s) is an MV-algebra.
- If s is a state-morphism, then X/ker(s) is a linearly ordered locally finite MV-algebra.
- s is a state-morphism on X.
- ker(s) is a maximal filter of X.
- s is extremal on X.
145.
The present paper is devoted to a micromechanical model of porous rocks and its application to a sandstone. This original model takes advantage of a recent homogenization-based macroscopic yield function which couples Drucker-Prager type plasticity of the solid matrix and evolving porosity. Its formulation and implementation are described. Application to a Vosges sandstone shows that, except for very low confining pressures for which the mechanical behavior is quasi-brittle, the model predicts well the ductile behavior at moderate or high confining pressures (for which the pore collapse mechanism is expected to play a dominant role). 相似文献
146.
Shin-ichiro Hayashi Munenori Yoshioka Shuji Usui Kiyofumi Haneda Takahiro Kondo Kim B. McAuley Takahiro Tominaga 《Radiation Physics and Chemistry》2010,79(7):803-808
In radiotherapy treatment, polymer gel dosimetry can be used for verifying three-dimensional (3D) dose distributions. Gelatin is generally used as a gelling agent in the dosimeters. In this paper, another role of gelatin in a methacrylic-acid-based gel dosimeter (MAGAT) is investigated. Temperature increases due to exothermic polymerization in the irradiated gel are measured directly. Dose–R2 responses are also obtained using MRI. It is shown that no appreciable increases in either temperature or R2 are observed in MAGAT dosimeters made without gelatin, and that significant temperature and R2 increases are observed when very low gelatin concentrations are used. These results indicate that gelatin is an important enabler for radiation-induced free-radical polymerization in methacrylic-acid-based gels. When gelatin is replaced by amino acids, changes in temperature are observed, along with small changes in R2. The resulting dosimeter solutions remain transparent because the polymer does not precipitate as it does in regular MAGAT dosimeters containing gelatin. When the amino acids are replaced by acids without amino groups, no temperature or R2 changes are observed, indicating that no polymer forms. These results show that amino groups (and possibly other functional groups) on the gelatin catalyze the radiation-induced free-radical polymerization that occurs in MAGAT dosimeters. 相似文献
147.
Effect of solvent composition on chiral recognition ability of molecularly imprinted DIDE derivatives. 总被引:2,自引:0,他引:2
In the present study, molecularly imprinted materials from the tetrapeptide derivative, H-Asp(OcHex)-Ile-Asp(OcHex)-Glu(OBzl)-CH2-, were adopted as samples to study the effect of the polarity of the environment on the chiral (molecular) recognition ability. The optimum composition, with the best chiral recognition, is a 50 vol% aqueous ethanol solution. 相似文献
148.
149.
P. G. Reutens F. S. Merritt M. J. Oreglia P. Auchincloss R. E. Blair C. Haber S. R. Mishra E. Oltman M. Ruiz F. J. Sciulli M. H. Shaevitz W. H. Smith R. Zhu R. Coleman H. E. Fisk B. Jin T. Kondo D. Levinthal W. Marsh P. A. Rapidis H. B. White D. Yovanovitch A. Bodek F. Borcherding N. Giokaris K. Lang I. E. Stockdale 《Zeitschrift fur Physik C Particles and Fields》1990,45(4):539-550
We report a measurement of the electroweak parameters sin2θ w and ? based on the ratios of neutral current to charged current events measured in the Fermilab narrow-band neutrino beam at energies of 30–240 GeV. The data are fully corrected for radiative effects, heavy-quark production, and other effects. The best value for sin2θ w obtained, sin2θ w =0.239±0.011, is consistent with the most recent values fromW andZ production, as well as from other neutrino experiments. 相似文献
150.
Sonochemistry of volatile and non-volatile solutes in aqueous solutions: e.p.r. and spin trapping studies 总被引:6,自引:0,他引:6
Recent spin trapping studies of the free radical intermediates generated by the sonolysis of aqueous solutions are reviewed. Studies of rare gas saturated solutions of volatile solutes (e.g., methanol and ethanol) and of non-volatile solutes (acetate, amino acids, sugars, pyrimidines, nucleotides and surfactants) are consistent with the theory of three reaction zones in aqueous sonochemistry. The very high temperatures and pressures induced by acoustic cavitation in collapsing gas bubbles in aqueous solutions lead to the thermal dissociation of water vapour into hydrogen atoms and hydroxyl radicals. Reactions take place in the gas phase (pyrolysis reactions), in the region of the gas-liquid interface, and in the bulk of the solution at ambient temperature (similar to radiation chemistry reactions). By use of the rare gases with different thermal conductivities, the contributions of individual reaction steps with widely different energies of activation can be evaluated. 相似文献