全文获取类型
收费全文 | 15786篇 |
免费 | 3065篇 |
国内免费 | 2383篇 |
专业分类
化学 | 8467篇 |
晶体学 | 183篇 |
力学 | 1613篇 |
综合类 | 150篇 |
数学 | 1106篇 |
物理学 | 9715篇 |
出版年
2024年 | 38篇 |
2023年 | 163篇 |
2022年 | 564篇 |
2021年 | 539篇 |
2020年 | 589篇 |
2019年 | 505篇 |
2018年 | 485篇 |
2017年 | 642篇 |
2016年 | 728篇 |
2015年 | 575篇 |
2014年 | 886篇 |
2013年 | 1340篇 |
2012年 | 1011篇 |
2011年 | 1088篇 |
2010年 | 923篇 |
2009年 | 1050篇 |
2008年 | 1068篇 |
2007年 | 982篇 |
2006年 | 1012篇 |
2005年 | 815篇 |
2004年 | 789篇 |
2003年 | 678篇 |
2002年 | 576篇 |
2001年 | 537篇 |
2000年 | 500篇 |
1999年 | 365篇 |
1998年 | 397篇 |
1997年 | 329篇 |
1996年 | 301篇 |
1995年 | 263篇 |
1994年 | 236篇 |
1993年 | 206篇 |
1992年 | 189篇 |
1991年 | 139篇 |
1990年 | 118篇 |
1989年 | 104篇 |
1988年 | 110篇 |
1987年 | 74篇 |
1986年 | 52篇 |
1985年 | 42篇 |
1984年 | 50篇 |
1983年 | 19篇 |
1982年 | 39篇 |
1981年 | 23篇 |
1980年 | 15篇 |
1979年 | 15篇 |
1978年 | 20篇 |
1977年 | 9篇 |
1976年 | 6篇 |
1973年 | 15篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
981.
The reactivity of ethyl‐, propyl‐ and octylgallate towards diphenylpicryl hydracil radicals has been measured in homogeneous solution (ethanol) and in Triton X‐100 micellar solutions. Similar reactivities were measured in homogeneous solutions, indicating that the length of the alkyl chain does not influence the reactivity of the phenolic groups. On the other hand, different reactivities were measured in micellar solutions, particularly at low (5 mM) surfactant concentrations. Data obtained at different surfactant concentrations allow estimation of partitioning of the gallates and their intramicellar bimolecular rate constant. The values obtained indicate that all the observed differences in reactivity are attributable to differences in substrate partitioning between the micellar and aqueous pseudophases. In fact, similar values of the intramicellar rate constants were obtained, suggesting that the average location of the reactive groups inside the micelles is independent of the solute alkyl chain length. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
982.
Yoshiteru Amemiya Tomohiro Tokunaga Yuichiro Tanushi Shin Yokoyama 《Optical Review》2009,16(3):247-251
Electric-field drive optical modulators using a Si ring resonator were fabricated on silicon-on-insulator (SOI) wafers. The
fabricated resonators consisted of Si waveguides with width and thickness of 1.0 and 0.3 μm, respectively. In order to induce
the linear electro-optic (EO) effect in the Si core layer, the strain was applied by covering the layer with Si3N4 film (0.26 μm thick) deposited by low pressure chemical vapor deposition (LPCVD) at 750 °C. The vertical electric-field was
applied to the Si waveguide through the top and bottom cladding layers, and the optical output from the drop port at the resonance
wavelength was measured. At a wavelength of 1501.6 nm, the optical modulation of 33% was obtained at 200V (electric-field
at the silicon surface ∼3 × 105 V/cm, nearly the breakdown field). The resonance wavelength was shifted toward the short wavelength side by applying both
positive and negative voltages, this shift was explained by carrier concentration modulation. The linear EO effect in the
Si core layer was not observed, presumably because the strain in the Si core layer was too small. 相似文献
983.
EDOT‐diketopyrrolopyrrole copolymers for high bulk hole mobility and near infrared absorption 下载免费PDF全文
Christian J. Mueller Chetan R. Singh Mukundan Thelakkat 《Journal of Polymer Science.Polymer Physics》2016,54(6):639-648
To obtain novel low‐bandgap materials with tailored hole‐transport properties and extended absorption, electron rich 3,4‐ethylenedioxythiophene is introduced as a comonomer in diketopyrrolo[3,4‐c]pyrrole copolymers with different aryl flanking units. The polymers are characterized by absorption and photoluminescence spectroscopy, dynamic scanning calorimetry, cyclic voltammetry, and X‐ray diffraction. The charge transport properties of these new materials are studied carefully using an organic field effect transistor geometry where the charge carriers are transported over a narrow channel at the semiconductor/dielectric interface. These results are compared to bulk charge carrier mobilities using space‐charge limited current (SCLC) measurements, in which the charge carrier is transported through the complete film thickness of several hundred nanometers. Finally, charge carrier mobilities are correlated with the electronic structure of the compounds. We find that in particular the thiophene‐flanked copolymer PDPP[T]2‐EDOT is a very promising candidate for organic photovoltaics, showing an absorption response in the near infrared region with an optical bandgap of 1.15 eV and a very high bulk hole mobility of 2.9 × 10?4 cm2 V?1 s?1 as measured by SCLC. This value is two orders of magnitudes higher than SCLC mobilities reported for other polydiketopyrrolopyrroles and is in the range of the well‐known hole transporting polymer poly(3‐hexylthiophene). © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 639–648 相似文献
984.
Cover Picture: Sequential Anion and Cation Exchange Reactions for Complete Material Transformations of Nanoparticles with Morphological Retention (Angew. Chem. Int. Ed. 30/2015) 下载免费PDF全文
985.
Experimental results on the extrapolated ultimate enhancement factors of o-, m-, and p-xylene protons at 1.53 mT are obtained for MC800 asphalt solutions. The ultimate enhancement factors are found such as ?26.9, ?25.7, and ?11.7 for o-, m-, and p-xylene, respectively. These results show that the solvent proton Overhauser effect cannot reach the extrapolated enhancement of ?330 in the extreme narrowing case because of occurrence of small scalar interactions in addition to the dipole–dipole interactions between solvent protons and asphalt electrons. The ortho, meta, and para positions of the –CH3 group change the nature of the interactions. The nuclear magnetic resonance (NMR) signal enhancements exhibit a sensitive behavior depending on the chemical environment differing from isomer to isomer. The solvation or association of asphalt in xylene isomers at room temperature is revealed. Quantum chemical calculations for the xylene isomers with the electronic and optical properties; absorption wavelengths, excitation energy, atomic charges, dipole moment and frontier molecular orbital energies, molecular electrostatic potential; are carried out using the density functional theory (DFT) method (B3LYP) with the 6-311G(d,p) basis set by the standard Gaussian 09 software package program. The relative importance of scalar and translational dipolar interaction parameters determined in dynamic nuclear polarization experiments is explained by the electronic structure of HOMO–LUMO of the xylene isomers. 相似文献
986.
Min Cheng 《辐射效应与固体损伤》2013,168(11-12):1083-1089
ABSTRACTThe EPR g factors g// and g⊥ for the tetragonal (CrO4)3? impurity center in ZrSiO4: Cr5+ crystal are studied from the high-order perturbation formulas based on the two-mechanism (the crystal field and charge-transfer mechanisms) model. The studies indicate that differing from the tetragonally-elongated host (SiO4)4- tetrahedron, the dominant defect structure of the substitutional (CrO4)3? tetrahedron is tetragonally- compressed with the ground state |dz2 due to the Jahn-Teller distortion. Furthermore, the agreement of g factors between calculation and experiment requires a small admixture of the first excited state |dx2?y2 to the ground state |dz2 due to the vibrational motion of ligands, which leads a compressed (CrO4)3? tetrahedron to become a twinkling elongated one, These results are discussed. 相似文献
987.
Serena Indelicato David Bongiorno Sergio Indelicato Laszlo Drahos Vincenzo Turco Liveri Lilla Turiák Karoly Vékey Leopoldo Ceraulo 《Journal of mass spectrometry : JMS》2013,48(3):379-383
The characteristic collision energy (CCE) to obtain 50% fragmentation of positively and negatively single charged noncovalent clusters has been measured. CCE was found to increase linearly with the degrees of freedom (DoF) of the precursor ion, analogously to that observed for synthetic polymers. This suggests that fragmentation behavior (e.g. energy randomization) in covalent molecules and clusters are similar. Analysis of the slope of CCE with molecular size (DoF) indicates that activation energy of fragmentation of these clusters (loss of a monomer unit) is similar to that of the lowest energy fragmentation of protonated leucine–enkephalin. Positively and negatively charged aggregates behave similarly, but the slope of the CCE versus DoF plot is steeper for positive ions, suggesting that these are more stable than their negative counterparts. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
988.
《Analytical letters》2012,45(7):1397-1412
Abstract Silicon nitride membrane ISFET sensor chips have been produced with varying gate dimensions. A series of width/length (W/L) aspect ratios have been examined, combined with three levels of boron ion-implant. The level of ion-implantation affects the threshold voltage; this is important as a low threshold voltage allows the use of low noise operating conditions. Gate dimensions are also important factors for they determine the level of drain current for a given gate and drain voltages. A novel design feature, aimed at achieving wide gates, is the use of folded gates as well as having a straight structure. The evaluation of devices with gates covered with poly(vinyl chloride) (PVC)-valinomycin-dioctyl adipate was based on their response to potassium chloride standards when it was shown that there may be a maximum width of gate above which there is no improvement of response. Also, the effect of folding the gate structure is discussed and shown to be tenable, thus permitting greater miniaturisation. 相似文献
989.
Milovan M. Stoiljković Igor A. Pašti Miloš D. Momčilović Jelena J. Savović Mirjana S. Pavlović 《Spectrochimica Acta Part B: Atomic Spectroscopy》2010
Enhancement of emission line intensities by induced oscillations of direct current (DC) arc plasma with continuous aerosol sample supply was investigated using multivariate statistics. Principal component analysis (PCA) was employed to evaluate enhancements of 34 atomic spectral lines belonging to 33 elements and 35 ionic spectral lines belonging to 23 elements. Correlation and classification of the elements were done not only by a single property such as the first ionization energy, but also by considering other relevant parameters. Special attention was paid to the influence of the oxide bond strength in an attempt to clarify/predict the enhancement effect. Energies of vaporization, atomization, and excitation were also considered in the analysis. In the case of atomic lines, the best correlation between the enhancements and first ionization energies was obtained as a negative correlation, with weak consistency in grouping of elements in score plots. Conversely, in the case of ionic lines, the best correlation of the enhancements with the sum of the first ionization energies and oxide bond energies was obtained as a positive correlation, with four distinctive groups of elements. The role of the gas-phase atom-oxide bond energy in the entire enhancement effect is underlined. 相似文献
990.
Laibin Zhang Huifang Li Jilai Li Xiaohua Chen Yuxiang Bu 《Journal of computational chemistry》2010,31(4):825-836
A comprehensive theoretical study of electronic transitions of naphtho‐homologated base analogs, namely, yy‐T , yy‐C , yy‐A , and yy‐G , was performed. The nature of the low‐lying excited states is discussed, and the results are compared with those from experiment and also with those of y‐bases. Geometrical characteristics of the lowest excited singlet ππ* and nπ* states were explored using the CIS method, and the effects of methanol solution and paring with their complementary natural bases on the relevant absorption and emission spectra of these modified bases were examined. The calculated excitation and emission energies agree well with the measured data, where experimental results are available. In methanol solution, the fluorescence from yy‐A and yy‐G would be expected to occur around 539 and 562 nm, respectively, suggesting that yy‐A is a green‐colored fluorophore, whereas yy‐G is a yellow‐colored fluorophore. The methanol solution was found to red‐shift both the absorption and emission maxima of yy‐A , yy‐T , and yy‐C , but blue‐shift those for yy‐G . Generally, though base pairing has no significant effects on the absorption and fluorescence maxima of yy‐A , yy‐C , and yy‐T , it blue‐shifts those for yy‐G . © 2009 Wiley Periodicals, Inc. J Comput Chem 2010 相似文献