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101.
102.
Improvement of thermal conductivity of poly(dimethyl siloxane) using silica-coated multi-walled carbon nanotube 总被引:1,自引:0,他引:1
Jinho Hong Jeongwoo Lee Chang Kook Hong Sang Eun Shim 《Journal of Thermal Analysis and Calorimetry》2010,101(1):297-302
In order to enhance the thermal conductivity of MWCNT filled poly(dimethyl siloxane) (PDMS) composites, the MWCNT was coated
with silica layer by three step reactions. The composites filled with raw and silica-coated MWCNTs were prepared and the properties
were investigated in terms of the curing characteristics, mechanical properties, and thermal conductivity. Due to the poor
compatibility between raw MWCNT and PDMS, raw MWCNT showed poor dispersion uniformity and wettability in PDMS. On the other
hand, due to the chemical affinity between silica/MWCNT and PDMS throughout the hydrogen bonding, the silica-coated MWCNT
filled PDMS showed improved mechanical properties in terms of tensile strength and 100% modulus, and good interfacial compatibility
than raw MWCNT incorporated PDMS. Finally, the good wettability of silica/MWCNT in PDMS resulted in higher thermal conductivity
caused from the facile phonon movement at the interface even with the smaller MWCNT contents. 相似文献
103.
Silyl-bridged dimers of a ppy-BMes(2) (ppy = 2-phenylpyridine, Mes = mesityl) photochrome were found to undergo photochromic switching involving a single boryl unit only. A through-space intramolecular energy transfer was found to be responsible for the single-chromophore isomerization phenomenon and fluorescence quenching. Steric congestion in the diboryl molecules was found to have an impact on photoisomerization quantum efficiency. 相似文献
104.
This paper introduces strategies for enhancement of a surface plasmon resonance (SPR) signal by adopting colloidal gold nanoparticles (AuNPs) and a SiO2 layer on a gold surface. AuNPs on SiO2 on a gold surface were compared with an unmodified gold surface and a SiO2 layer on a gold surface with no AuNPs attached. The modified surfaces showed significant changes in SPR signal when biomolecules were attached to the surface as compared with an unmodified gold surface. The detection limit of AuNPs immobilized on a SPR chip was 0.1 ng mL−1 for the prostate-specific antigen (PSA), a cancer marker, as measured with a spectrophotometer. Considering that the conventional ELISA method can detect ∼10 ng mL−1 of PSA, the strategy described here is much more sensitive (∼100 fold). The enhanced shift of the absorption curve resulted from the coupling of the surface and particle plasmons by the SiO2 layer and the AuNPs on the gold surface. 相似文献
105.
Na K Jung J Shin B Hyun J 《Langmuir : the ACS journal of surfaces and colloids》2006,22(26):10889-10892
The development of a simple and easily accessible method to control cellular behavior under a spatially controlled surface is critical for fundamental studies in biotechnology. We fabricated a microarray of Spodoptera frugiperda 9 (Sf9) cells on a glass surface by microcontact printing cell-repellent polymeric molecules of poly(ethylene glycol)-branched-poly(methyl methacrylate) as a template for cell micropatterning. The polymer micropatterns enabled the stable confinement of Sf9 cells on the surface, resulting in the formation of a cell microarray. Subsequently, the patterned Sf9 cells were infected with recombinant baculovirus modified with green fluorescent protein (GFP) to form a virus microarray, and GFP expression in the virus microarray was verified with confocal fluorescence microscopy. 相似文献
106.
Dielectrophoresis of surface conductance modulated single-walled carbon nanotubes using catanionic surfactants 总被引:1,自引:0,他引:1
Kim Y Hong S Jung S Strano MS Choi J Baik S 《The journal of physical chemistry. B》2006,110(4):1541-1545
Dielectrophoresis has received considerable attention for separating nanotubes according to electronic types. Here we examine the effects of surface conductivity of semiconducting single walled carbon nanotubes (SWNT), induced by ionic surfactants, on the sign of dielectrophoretic force. The crossover frequency of semiconducting SWNT increases rapidly as the conductivity ratio between the particle and medium increases, leading to an incomplete separation of ionic surfactant suspended SWNT at an electric field frequency of 10 MHz. To reduce the conductivity ratio, the surface charge of SWNT is neutralized by an equimolar mixture of anionic surfactant sodium dodecyl sulfate (SDS) and cationic surfactant cetyltrimethylammonium bromide (CTAB), resulting in negative dielectrophoresis of semiconducting species at 10 MHz. A comparative Raman spectroscopy study shows a nearly complete separation of metallic SWNT. 相似文献
107.
108.
109.
Lee T Jeon J Song KH Jung I Baik C Park KM Lee SS Kang SO Ko J 《Dalton transactions (Cambridge, England : 2003)》2004,(6):933-937
An efficient 1,2-dehydrocarborane precursor, phenyl[o-(trimethylsilyl)carboranyl]iodonium acetate, was readily prepared by reaction of [o-(trimethylsilyl)carboranyl]lithium and IPh(OAc)2. The facile 2+4 cycloaddition of with dienes such as anthracene, naphthalene, norborna-2,5-diene and 2,5-dimethylfuran gave high yields of the 1,2-dehydrocarborane adducts in the presence of a desilylating agent. The reaction of with a cyclic alkene and strained cycloalkynes afforded the adducts formed by the ene reaction and the 2+2 cycloaddition reaction. The reaction of with a bicyclopalladacycle yielded the cyclization product. The structures of compounds and were determined by single-crystal X-ray crystallography. 相似文献
110.
Baik MH Gherman BF Friesner RA Lippard SJ 《Journal of the American Chemical Society》2002,124(49):14608-14615
The electronic structures of key species involved in methane hydroxylation performed by the hydroxylase component of soluble methane monooxygenase (sMMO), as proposed previously on the basis of high-level density functional theory, were investigated. The reaction starts with initial approach of methane at one of the bridging oxo atoms in intermediate Q, a di(mu-oxo)diiron(IV) unit. This step is accompanied by a proton-coupled outer-sphere transfer of the first electron from a C-H sigma-bond in methane to one of the metal centers. The second electron transfer, also an outer-sphere electron transfer process, occurs along a two-component reaction pathway. Both redox reactions are strongly coupled to structural distortions of the diiron core. The electronic consequence and driving force of these distortions are intuitively explained by using the computed Kohn-Sham orbitals in the broken-symmetry framework to incorporate the experimentally observed antiferromagnetic coupling of the unpaired electrons at the metal centers. The broken-symmetry orbital scheme is essential for describing the C-H bond activation process in a consistent and complete manner, enabling derivation of both an intuitive and quantitative understanding of the most salient electronic features that govern the details of the hydroxylation. 相似文献