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1.
Bao Nguyen Xuan Duy Khanh Phan Quoc Tung Nguyen Minh 《Set-Valued and Variational Analysis》2022,30(2):465-486
Set-Valued and Variational Analysis - We aim to establish Karush-Kuhn-Tucker multiplier rules involving higher-order complementarity slackness under Hölder metric subregularity. These rules... 相似文献
2.
Nguyen Minh Chuong Bui Kien Cuong 《Proceedings of the American Mathematical Society》2004,132(12):3589-3597
A class of Cauchy problems for interesting complicated periodic pseudodifferential equations is considered. By the Galerkin-wavelet method and with weak solutions one can find sufficient conditions to establish convergence estimates of weak Galerkin-wavelet solutions to a Cauchy problem for this class of equations.
3.
Summary Cold neutrons at the external neutron guide laboratory (ELLA) of the KFA Jülich are used to demonstrate their profitable application
for multielement characterization of biological materials. The set-up and experimental conditions of the Prompt Gamma Cold
Neutron Activation Analysis (PGCNAA) device is described in detail. Results for C, H, N, S, K, B, and Cd using synthetic standards
and the “ratio” technique for calculation are reported for several reference materials and prove the method to be reliable
and complementary with respect to the elements being determined by INAA.
IAEA fellow at the KFA from 6. 3. 91 to 2. 9. 91 on contract No. VIE/9016R. 相似文献
4.
Dragomir Ž. Đoković 《Combinatorica》1994,14(3):375-377
No Hadamard matrices of order 956 appear in the literature. In this note we construct two such matrices. They are both of Goethals-Seidel type. As a consequence of this and of a result of Seberry and Yamada, we conclude that there exist 4-Williamson type matrices of order 1913.This work was supported by NSERC of Canada Grants A-5285 and EQP0107539. 相似文献
5.
Tran Quang Minh Léon Christiaens Pierre Grandclaudon Alain Lablache-Combier 《Tetrahedron》1977,33(17):2225-2229
Photoirradiated in presence of acetophenone, benzo[b]selenophene and its 3-methyl derivative add to dimethyl acetylenedicarboxylate. In each ease, the primary reaction product is unstable and has not been isolated. Photoexeited in its triplet state (the energy of which is in the neighbourhood of 69 ) benzo[b]selenophene and its 2- and 3-methyl, 2,3 dimethyl, 3 acetoxy and 2-methyl-3-acetoxy derivatives add to 1,2 dichloroethylene leading to cyclobutanes. Neither cyclo-addition occurs in absence of photosensitiser. Single-crystal X-ray analysis gave the structures of the two adducts of 3-acetoxybenzo[b]selenophene with trans-1,2-dichloroethylene. In both compounds the chlorine atoms are trans. 相似文献
6.
Five new natural labdane-type diterpenoids (5-9), designated leoheteronins A-E, together with four known diterpenoids (1-4), two phytosterols as a mixture of beta-sitosterol and stigmasterol, and the flavone genkwanin (10) were isolated from the aerial parts of Leonurus heterophyllus SW. (Lamiaceae) collected in northern Vietnam. Compound 1 was isolated for the first time from a Leonurus species, and 10 is considered to be a chemotaxonomic marker of the Leonurus genus. Their structures were determined using spectroscopic analyses. 相似文献
7.
Pham-Tran NN Bouchoux G Delaere D Nguyen MT 《The journal of physical chemistry. A》2005,109(12):2957-2963
We have investigated the basicity of phosphinine (C5H5P, phosphabenzene) in reevaluating its proton affinity (PA) and gas-phase basicity (GB) and the pK(a) value of its protonated form. As a necessary step, we have first determined its gas-phase proton affinity. Using both mass spectrometric and quantum chemical methods, we have obtained the values PA(C5H5P) = 195.8 +/- 1.0 kcal mol(-1) and GB(298)(C5H5P) = 188.1 +/- 1.0 kcal mol(-1), in good agreement with previous results. We then derived a value of pK(a)(C5H6P+) = -16.1 +/- 1.0 in aqueous solution using three different approaches: the latter markedly differs from the currently available value of -10. The reason for such a discrepancy in the pK(a) of protonated phosphinine in solution is discussed. In the theoretical determination of PAs, evaluation of the basis set superposition error (BSSE) showed that this effect is quite small, being 0.1-0.2 kcal mol(-1) for phosphinine, when a density functional theory (DFT) method in conjunction with a large basis set were used. 相似文献
8.
We study a class of quasilinear elliptic equations on the unit ball of ℝ
n
in the divergence form ∑
j=1
n
D
j{G(|x|2,|Du|2)D
j
u} =H(|x|) and get estimates on the boundary by using a modified barrier-function technique of Bernstein. We establish a maximum principle
for the gradients of solutions and get a global gradient estimate. We prove that solutions with constant boundary condition
must be radial. Finally, we apply these results to graphs {(x,u(x)):x∈H
n
} whereu:H
n
→ℝ is a smooth map of then-hyperbolic spaceH
n
=B(0,1) with the metric
to get the existence of graphs with radial prescribed mean curvature. 相似文献
9.
LetK be an algebraically closed field withp:=char (K)>0 andX a bielliptic curve over Spec(K) with genus≥6 and such that the canonical model ofX is ordinary. In this paper we determine all the possible gap sequences of Weierstrass points on such curves. 相似文献
10.
T. Hiep Nguyen Peter S. Clezy Gary D. Willett George L. Paul John Tann Peter J. Derrick 《Journal of mass spectrometry : JMS》1991,26(4):215-226
Laser desorption Fourier transform ion cyclotron resonance positive- and negative-ion mass spectra are presented for dimethyl 8-acetyl-3,7,12,17-tetramethylporphyrin-2,18-dipropanoate. The 248-nm laser ionization thresholds for both positive and negative ions are observed to be about 2.5 MW cm?2. The M+˙ molecular ion is assigned to the base peak in the low-power spectra whereas it is the M?˙ ion for the corresponding anion spectra. Increased intensities of [M + H]+ and [M ? H]? are observed with increased laser fluences of up to 38 MW cm?2. At high laser powers the negative-ion results reveal that a series of carbon-nitrogen cumulene and polyacetylene cluster ions are formed. Laser evaporation/multiphoton ionization/ and thermal evaporation/electron impact ionization/collision-induced dissociation experiments carried out on the porphyrin M+˙ and [M + H]+ ions over a range of translational kinetic energies and delay times after acceleration are compared and used to obtain mechanistic and structural information. In contrast to the electron impact experiments, which show only side-chain cleavage, the laser-based collision-induced dissociation experiments reveal that, in addition to side-chain cleavage, it is possible to cleave the porphyrin ring to various extents depending on the ion translational energy selected. 相似文献