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51.
非线性Schr(o)dinger方程的一个新的守恒差分格式 总被引:2,自引:0,他引:2
本文对非线性Schrodinger方程提出了一种新的带参数的守恒差分格式,并证明了该格式的收敛性与稳定性,通过数值计算获得如下结论,本文提出的差分格式在取适当的参数后,精度上比ZhangFei等人(1995)的格式有较大幅度的提高。 相似文献
52.
Juan Li Huamei Qi Huan Wang Zhanjun Yang Peizhi Zhu Guowang Diao 《Mikrochimica acta》2014,181(9-10):1109-1115
A multiplexed assay strategy was developed for the detection of nucleic acid hybridization. It is based on fluorescence resonance energy transfer (FRET) between gold nanoparticles (AuNPs) and multi-sized quantum dots (QDs) deposited on the surface of silica photonic crystal beads (SPCBs). The SPCBs were first coated with a three-layer primer film formed by the alternating adsorption of poly(allylamine hydrochloride) and poly(sodium 4-styrensulfonate). Probe DNA sequences were then covalently attached to the carboxy groups at the surface of the QD-coated SPCBs. On addition of DNA-AuNPs and hybridization, the fluorescence of the donor QDs is quenched because of the close proximity of the AuNPs. However, the addition of target DNA causes a recovery of the fluorescence of the QD-coated SPCBs, thus enabling the quantitative assay of hybridized DNA. Compared to fluorescent dyes acting as acceptors, the use of AuNPs results in much higher quenching efficiency. The multiplexed assay displays a wide linear range, high sensitivity, and very little cross-reactivity. This work, where such SPCBs are used for the first time in a FRET assay, is deemed to present a new and viable approach towards high-throughput multiplexed gene assays. Figure
A novel fluorescence energy transfer system was constructed for the multiplexed hybridization assay using gold nanoparticles and quantum dot conjugates on silica photonic crystal beads 相似文献
53.
By employing the dissociation energy and the equilibrium bond length for a diatomic molecule as explicit parameters, we generate improved expressions for the well-known Rosen-Morse, Manning-Rosen, Tietz, and Frost-Musulin potential energy functions. It is found that the well-known Tietz potential function that is conventionally defined in terms of five parameters [T. Tietz, J. Chem. Phys. 38, 3036 (1963)] actually only has four independent parameters. It is shown exactly that the Wei [Phys. Rev. A 42, 2524 (1990)] and the well-known Tietz potential functions are the same solvable empirical function. When the parameter h in the Tietz potential function has the values 0, +1, and -1, the Tietz potential becomes the standard Morse, Rosen-Morse, and Manning-Rosen potentials, respectively. 相似文献
54.
In order to predict the extraction ability of 12-crown-4 for different metallic ions, the complexes [M(12-crown-4)] and [M(H2O)4] (where M=Li+, Na+, K+, Be2+, Mg2+, Ca2+, Cu2+ and Zn2+) were investigated by the density functional theory without restrictions for their geometry. The metal binding capability
was evaluated using the binding energy, and the effect of nature of the metal on the binding properties was also studied.
The results of the calculations showed that the coordination ability of a donor molecule towards different metal ions increased
in proportion to their ionization potential. In addition, based on the extraction distribution coefficient, we found that
12-crown-4 can selectively extract Cu2+ and Be2+ ions from aqueous solutions of mixed cations. Obviously, the stability of complexes and the extraction power of extractants
depend greatly on the nature of the metal ions. Calculation results from our study could be used to predict the extraction
power of this crown ether and could play a guiding role in planning experiments. 相似文献
55.
The effect of a static magnetic field on the evolution of hydrogen gas from a small platinum electrode in an aqueous electrolyte has been studied by recording the noise spectrum of overpotential voltage fluctuations at a constant current density of ?50 mA mm?2. A 1/f2 variation of the power spectrum characteristic of droplet coalescence is found for frequencies >10 Hz. The overpotential for hydrogen evolution decreases with applied field. When the production of gas bubbles is quasiperiodic, there is a threshold field of 0.5 T beyond which the size of the bubbles released is approximately doubled. This is explained by enhanced coalescence of small bubbles swept across the electrode surface by forced convection due to the Lorentz force. 相似文献
56.
Yun‐Peng Diao Kun Li Shan‐Shan Huang Xiao‐Hong Shu Ke‐Xin Liu Xu‐Ming Deng 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(2):m82-m85
In the mixed‐ligand metal–organic polymeric compound poly[[μ2‐1,4‐bis(imidazol‐1‐yl)benzene](μ2‐terephthalato)dizinc(II)], [Zn2(C8H4O4)2(C12H10N4)]n or [Zn2(bdc)2(bib)]n [H2bdc is terephthalic acid and bib is 1,4‐bis(imidazol‐1‐yl)benzene], the asymmetric unit contains one ZnII ion, with two half bdc anions and one half bib molecule lying around inversion centers. The ZnII ion is in a slightly distorted tetrahedral environment, coordinated by three carboxylate O atoms from three different bdc anions and by one bib N atom. The crystal structure is constructed from the secondary building unit (SBU) [Zn2(CO2)2N2O2], in which the two metal centers are held together by two bdc linkers with bis(syn,syn‐bridging bidentate) bonding modes. The SBU is connected by bdc bridges to form a two‐dimensional grid‐like (4,4)‐layer, which is further pillared by the bib ligand. Topologically, the dinuclear SBU can be considered to be a six‐connected node, and the extended structure exhibits an elongated primitive approximately cubic framework. The three‐dimensional framework possesses a large cavity with dimensions of approximately 10 × 13 × 17 Å in cross‐section. The potential porosity is filled with mutual interpenetration of two identical equivalent frameworks, generating a novel threefold interpenetrating network with an α‐polonium topology [Abrahams, Hoskins, Robson & Slizys (2002). CrystEngComm, 4 , 478–482]. 相似文献
57.
58.
H Zhou GW Diao SY Qian XZ Yang AH Yuan Y Song YZ Li 《Dalton transactions (Cambridge, England : 2003)》2012,41(35):10690-10697
The reaction of [W(CN)(8)](3-) with Ln(3+) and pyrazine in acetonitrile yielded a series of isostructural compounds formulated as Ln(H(2)O)(4)(pyrazine)(0.5)W(CN)(8) (Ln = La(1), Ce(2), Pr(3), Nd(4), Sm(5), Eu(6), Gd(7)). The Ln(iii) and W(v) centers in the structure are linked through cyanide groups to form two-dimensional (2D) layers, which are further pillared by pyrazine, generating 3D frameworks. The magnetic behavior for compounds 1-7 were driven by the lanthanide ions involved. The Ln(iii) and W(v) ions in compounds 2 and 5 are ferromagnetically coupled with magnetic ordering occurring at 2.8 K, comparable with magnetic ordering with the critical temperature of 1.9 K for compound 4. In addition, the antiferromagnetic interactions were observed in compounds 3 and 7, while no significant magnetic couplings were found in compounds 1 and 6. 相似文献
59.
A simple and sensitive fluorimetric method for the determination of ascorbic acid (AA) is described. The method is based on the condensation reaction between AA and o-phenylenediamine (OPDA) in the absence of the oxidant. The fluorescence intensity is measured at excitation and emission wavelengths of 360 and 430 nm, respectively. Under optimum condition, a linear relationship is obtained between the fluorescence intensity and the concentration of AA in the range of 0.05-40 μg ml−1. The detection limit is 0.006 μg ml−1, which is obviously lower than that of other fluorimetric methods reported. 相似文献
60.
MnO2‐Modified Persistent Luminescence Nanoparticles for Detection and Imaging of Glutathione in Living Cells and In Vivo 下载免费PDF全文
Dr. Na Li Wei Diao Yaoyao Han Dr. Wei Pan Tingting Zhang Prof. Bo Tang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(50):16488-16491
Persistent luminescence nanoparticles (PLNPs) hold great promise for the detection and imaging of biomolecules. Herein, we have demonstrated a novel nanoprobe, based on the manganese dioxide (MnO2)‐modified PLNPs, that can detect and image glutathione in living cells and in vivo. The persistent luminescence of the PLNPs can be efficiently quenched by the MnO2 nanosheets. In the presence of glutathione (GSH), MnO2 was reduced to Mn2+ and the luminescence of PLNPs can be restored. The persistent luminescence property can allow detection and imaging without external excitation and avoid the background noise originating from the in situ excitation. This strategy can offer a promising platform for detection and imaging of reactive species in living cells or in vivo. 相似文献