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排序方式: 共有327条查询结果,搜索用时 62 毫秒
321.
Lindh L Svendsen IE Svensson O Cárdenas M Arnebrant T 《Journal of colloid and interface science》2007,310(1):74-82
In situ ellipsometry was used to study layer-by-layer film formation on hydrophilic and hydrophobized silica surfaces by alternating sequential adsorption of human mucin MUC5B and cationic proteins lysozyme, lactoferrin, lactoperoxidase or histatin 5, respectively. The stability of the multilayers was investigated by addition of sodium dodecyl sulfate solution (SDS). Atomic force microscopy was employed to investigate morphological structures on the surfaces during the layer-by-layer film build-up. It was clearly shown that, on both hydrophilic and hydrophobized silica, only MUC5B and lactoperoxidase showed the ability for multilayer formation, resulting in an approximately linear increase in adsorbed amount and film thickness with each deposition cycle. The net increase in amounts per cycle was larger on the hydrophilic silica. Further, MUC5B needs to be adsorbed first on the hydrophilic substrates to obtain this fast build-up behavior. Generally, addition of SDS solution showed that a large fraction of the adsorbed film could be desorbed. However, films on the hydrophobized silica were more resistant to surfactant elution. In conclusion, MUC5B-cationic protein multilayers can be formed on hydrophilic and hydrophobized silica, depending on the choice of the cationic protein as well as in which order the build-up is started on hydrophilic silica. Additionally, SDS disrupts the layer-by-layer film formed by MUC5B and lactoperoxidase. 相似文献
322.
Olof Johansson Hervé Mutelle Alexander E. Parker Sébastien Batut Pascal Demaux Coralie Schoemaecker Christa Fittschen 《Applied physics. B, Lasers and optics》2014,114(3):421-432
An instrument implementing Incoherent BroadBand Cavity-Enhanced Absorption Spectroscopy (IBBCEAS) for quantitative measurements of molecular iodine (I2) at ambient pressure and in the presence of aerosols is presented. The instrument is based on a LED emitting in the green spectral region around 500–550 nm, exciting a multitude of rovibronic transitions in the I2 B ← X electronic absorption spectrum. I2 was generated using a permeation device and was mixed with a dilution flow of Ar and another flow containing NaCl aerosols. Retrieval of the mirror reflectivity, necessary for quantitative IBBCEAS measurements, was not pursued in this study. Instead, calibrated I2 flows were used, and a differential optical absorption spectroscopy type of algorithm was implemented for the data analysis. This approach has several benefits, in particular when light extinction due to aerosols is substantial. Estimated detection limits are roughly 0.04 nmol/l without aerosols and 0.4 nmol/l in the presence of aerosols (1010 particles/l with 60–70 nm mean diameter, leading to I 0/I aerosols ≈ 5.4). A drop in measured I2 concentration in relation to the expected mixing ratio was observed when using the highest aerosol concentration, likely due to adsorption of I2 onto aerosols. 相似文献
323.
Anders Lundgren Mats Hulander Joakim Brorsson Malte Hermansson Hans Elwing Olof Andersson Bo Liedberg Mattias Berglin 《Particle & Particle Systems Characterization》2014,31(2):209-218
A simple and efficient principle for nanopatterning with wide applicability in the sub‐50 nanometer regime is chemisorption of nanoparticles; at homogeneous substrates, particles carrying surface charge may spontaneously self‐organize due to the electrostatic repulsion between adjacent particles. Guided by this principle, a method is presented to design, self‐assemble, and chemically functionalize gradient nanopatterns where the size of molecular domains can be tuned to match the level corresponding to single protein binding events. To modulate the binding of negatively charged gold nanoparticles both locally (<100 nm) and globally (>100 μm) onto a single modified gold substrate, ion diffusion is used to achieve spatial control of the particles’ mutual electrostatic interactions. By subsequent tailoring of different molecules to surface‐immobilized particles and the void areas surrounding them, nanopatterns are obtained with variable chemical domains along the gradient surface. Fimbriated Escherichia coli bacteria are bound to gradient nanopatterns with similar molecular composition and macroscopic contact angle, but different sizes of nanoscopic presentation of adhesive (hydrophobic) and repellent poly(ethylene) glycol (PEG) domains. It is shown that small hydrophobic domains, similar in size to the diameter of the bacterial fimbriae, supported firmly attached bacteria resembling catch‐bond binding, whereas a high number of loosely adhered bacteria are observed on larger hydrophobic domains. 相似文献
324.
Deng L Norberg O Uppalapati S Yan M Ramström O 《Organic & biomolecular chemistry》2011,9(9):3188-3198
A series of light-activatable perfluorophenylazide (PFPA)-conjugated carbohydrate structures have been synthesized and applied to glycoarray fabrication. The glycoconjugates were structurally varied with respect to anomeric attachment, S-, and O-linked carbohydrates, respectively, as well as linker structure and length. Efficient stereoselective synthetic routes were developed, leading to the formation of the PFPA-conjugated structures in good yields over few steps. The use of glycosyl thiols as donors proved especially efficient and provided the final compounds in up to 70% total yield with high anomeric purities. PFPA-based photochemistry was subsequently used to generate carbohydrate arrays on a polymeric surface, and surface plasmon resonance imaging (SPRi) was applied for evaluation of carbohydrate-protein interactions using the plant lectin Concanavalin A (Con A) as a probe. The results indicate better performance and equal efficiency of S- and O-linked structures with intermediate linker length. 相似文献
325.
Schöbel H Leidlmair C Bartl P Aleem A Hager M Echt O Märk TD Scheier P 《Physical chemistry chemical physics : PCCP》2011,13(3):1092-1098
Helium nanodroplets are co-doped with C(60) and ammonia. Mass spectra obtained by electron ionization reveal cations containing ammonia clusters complexed with up to four C(60) units. The high mass resolution of Δm/m≈ 1/6000 makes it possible to separate the contributions of protonated, unprotonated and dehydrogenated ammonia. C(60) aggregates suppress the proton-transfer reaction which usually favors the appearance of protonated ammonia cluster ions. Unprotonated C(x)(NH(3))(n)(+) ions (x = 60, 120, 180) exceed the abundance of the corresponding protonated ions if n < 5; for larger values of n the abundances of C(60)(NH(3))(n)(+) and C(60)(NH)(n-1)NH(4)(+) become about equal. Dehydrogenated C(60)NH(2)(+) ions are relatively abundant; their formation is attributed to a transient doubly charged C(60)-ammonia complex which forms either by an Auger process or by Penning ionization following charge transfer between the primary He(+) ion and C(60). The abundance of C(x)NH(3)(+) and C(x)NH(4)(+) ions (x = 120 or 180) is one to two orders of magnitude weaker than the abundance of ions containing one or two additional ammonia molecules. However, a model involving evaporation of NH(3) or NH(4) from the presumably weakly bound C(x)NH(3)(+) and C(x)NH(4)(+) ions is at odds with the lack of enhancement in the abundance of C(120)(+) and C(180)(+). Mass spectra of C(60) dimers complexed with water complement a previous study of C(60)(H(2)O)(n)(+) recorded at much lower mass resolution. 相似文献
326.
Davide Derelli Francesco Caddeo Kilian Frank Kilian Krötzsch Patrick Ewerhardt Marco Krüger Sophie Medicus Lars Klemeyer Marvin Skiba Charlotte Ruhmlieb Olof Gutowski Ann-Christin Dippel Wolfgang J. Parak Bert Nickel Dorota Koziej 《Angewandte Chemie (International ed. in English)》2023,62(43):e202307948
CuBi2O4 has recently emerged as a promising photocathode for photo-electrochemical (PEC) water splitting. However, its fast degradation under operation currently poses a limit to its application. Here, we report a novel method to study operando the semiconductor-electrolyte interface during PEC operation by surface-sensitive high-energy X-ray scattering. We find that a fast decrease in the generated photocurrents correlates directly with the formation of a metallic Bi phase. We further show that the slower formation of metallic Cu, as well as the dissolution of the electrode in contact with the electrolyte, further affect the CuBi2O4 activity and morphology. Our study provides a comprehensive picture of the degradation mechanisms affecting CuBi2O4 electrodes under operation and poses the methodological basis to investigate the photocorrosion processes affecting a wide range of PEC materials. 相似文献
327.
We compute the rational Betti cohomology groups of the coarse moduli spaces of geometrically marked Del Pezzo surfaces of degree 3 and 4 as representations of the Weyl groups of the corresponding root systems. The proof uses a blend of methods from point counting over finite fields and techniques from arrangement complements. 相似文献