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81.
Kee Sung Han Seong-Soo Kim Ki Hyeok Kang Byoung Jean Mean Heon Hwa Choi Oc Hee Han Moohee Lee 《Electrochemistry communications》2009,11(2):466-468
195Pt nuclear magnetic resonance (NMR) was employed to study the influence of Nafion ionomers (NIs), a common ingredient used as a proton conducting mediator and binder in a membrane-electrode-assembly (MEA) for proton exchange membrane fuel cells, on the local density of states at the Fermi surface (EF-LDOS) of Pt/C catalysts. NIs were observed to increase the surface EF-LDOS of Pt particles, thereby altering of the catalytic properties of metal particles. This correlates well with the reduction of fuel oxidation rates. Thus, ionomers decreasing the surface EF-LDOS of Pt particles would be desirable. In addition, a new concept to interpret the surface EF-LDOS was introduced and validated. 相似文献
82.
Imide-siloxane block copolymer/silica hybrid membranes: preparation, characterization and gas separation properties 总被引:1,自引:0,他引:1
Ho Bum Park Jang Ki Kim Sang Yong Nam Young Moo Lee 《Journal of membrane science》2003,220(1-2):59-73
Imide-siloxane block copolymer/silica hybrid membranes with covalent bonds were prepared via sol–gel reaction. The structural informations of these hybrid membranes were obtained by using Fourier transform-infrared spectrometry (FT-IR), 29Si nuclear magnetic resonance (29Si NMR), XPS and thermogravimetric analysis (TGA). The gas separation properties of the hybrid membranes were also investigated in terms of organosiloxane (PDMS) or silica content at various temperatures. In the hybrids, the addition of PDMS phase increased the permeabilities of gases such as He, CO2, O2, and N2, indicating that the gas transport occurred mainly through rubbery organic matrix. Meanwhile, the PDMS phase contributed the decreased gas selectivities to nitrogen but the reduction in selectivities was very small in comparison with other siloxane containing polymeric membranes. This might be due to the restriction of chain mobility by the existence of inorganic component such as silica network in the hybrids. Additionally, the increase of silica content in these hybrid membranes considerably retarded the falling-off of gas selectivity at elevated temperature. The increase of silica content in hybrid membranes resulted in well-formed silica networks and hence these inorganic components restricted the plasticization of organic matrix by the thermal segmental motion of organic components, leading to preventing the large decrease of the gas selectivity. 相似文献
83.
Cyclometalated Palladium(II) N‐Heterocyclic Carbene Complexes: Anticancer Agents for Potent In Vitro Cytotoxicity and In Vivo Tumor Growth Suppression 下载免费PDF全文
Dr. Tommy Tsz‐Him Fong Dr. Chun‐Nam Lok Dr. Clive Yik‐Sham Chung Dr. Yi‐Man Eva Fung Dr. Pui‐Keong Chow Pui‐Ki Wan Prof. Dr. Chi‐Ming Che 《Angewandte Chemie (International ed. in English)》2016,55(39):11935-11939
Palladium(II) complexes are generally reactive toward substitution/reduction, and their biological applications are seldom explored. A new series of palladium(II) N‐heterocyclic carbene (NHC) complexes that are stable in the presence of biological thiols are reported. A representative complex, [Pd(C^N^N)(N,N′‐nBu2NHC)](CF3SO3) ( Pd1 d , HC^N^N=6‐phenyl‐2,2′‐bipyridine, N,N′‐nBu2NHC=N,N′‐di‐n‐butylimidazolylidene), displays potent killing activity toward cancer cell lines (IC50=0.09–0.5 μm ) but is less cytotoxic toward a normal human fibroblast cell line (CCD‐19Lu, IC50=11.8 μm ). In vivo anticancer studies revealed that Pd1 d significantly inhibited tumor growth in a nude mice model. Proteomics data and in vitro biochemical assays reveal that Pd1 d exerts anticancer effects, including inhibition of an epidermal growth factor receptor pathway, induction of mitochondrial dysfunction, and antiangiogenic activity to endothelial cells. 相似文献
84.
Choi EY Kim D Hong BK Kwon HM Song YG Byun KH Park HY Whang KC Kim HS 《Experimental & molecular medicine》2002,34(6):391-400
Chlamydia pneumoniae infection implicated as an important etiologic factor of atherosclerosis, especially in coronary artery disease (CAD), was found in vitro to be associated with the induction of matrix metalloproteinases (MMPs). An extracellular matrix metalloproteinase inducer (EMMPRIN)/ membrane-type 1 matrix metalloproteinase (MT1-MMP) system which induces and activates MMPs, is suggested to be functional and were upregulated in the failing myocardium. However, the upstream regulation of MMPs by C. pneumoniae within atheroma itself remains unclear. We evaluated the seroepidemiologic study of C. pneumoniae infection in CAD patients (n= 391) and controls (n=97) and performed histopathological and in vitro analysis in atherosclerotic vascular tissues obtained from patients with seropositive to C. pneumoniae (n=20), by using immunochemistry for C. pneumoniae, EMMPRIN/MT1-MMP, MMP-2, and MMP-9. The seropositive rates of both anti-C. pneumoniae IgG and IgA were 56.7% in CAD group and 43.3% in control group (P=0.033). Seropositive rate was increased in subgroups of CAD patients without conventional coronary risk factors compared to those with conventional risk factors. Immunoreactivities of EMMPRIN, MT1-MMP, MMP-2, and MMP-9 were increased in the atheromatous plaque itself, predominantly in immunoreactive macrophages/mononuclear cells to C. pneumoniae. Furthermore, Western blot analysis showed that EMMPRIN and MMP-2 were detected more prominently in atherosclerotic tissues infected with C. pneumoniae compared to control tissues. Zymographic analysis revealed that activities of MMP-2 and MMP-9 were more increased in atherosclerotic tissues infected with C. pneumoniae compared to control tissues. The present study demonstrated upstream regulation of MMPs can be induced by C. pneumoniae within atheromatous plaque itself. These findings help to understand the potential role of C. pneumoniae in the progression of atherosclerosis. 相似文献
85.
K.S. Kim Myung Ki Cheoun Yeungun Chung Hyung Joo Nam 《The European Physical Journal A - Hadrons and Nuclei》2001,11(2):147-154
New results for the double beta decay of 76
Ge are presented. They are extracted from data obtained with the HEIDELBERG-MOSCOW experiment, which operates five enriched
76
Ge detectors in an extreme low-level environment in the Gran Sasso underground laboratory. The two-neutrino-accompanied double
beta decay is evaluated for the first time for all five detectors with a statistical significance of 47.7 kg y resulting in
a half-life of T
1/2
2ν = [1.55±0.01(stat)+0.19
-0.15(syst)]×1021 y. The lower limit on the half-life of the 0νββ decay obtained with pulse shape analysis is T
1/2
0ν > 1.9×1025(3.1×1025) y with 90% C.L. (68% C.L.) (with 35.5 kg y). This results in an upper limit of the effective Majorana-neutrino mass of 0.35
eV (0.27 eV) using the matrix elements of A. Staudt et al.'s work (Europhys. Lett. 13, 31 (1990)). This is the most stringent limit at present from double beta decay. No evidence for a majoron-emitting decay
mode is observed.
Received: 22 August 2001 / Accepted: 18 October 2001 相似文献
86.
Jang HS Ryu KE Ahn WS Chun HJ Dal Park H Park KD Kim YH 《Colloids and surfaces. B, Biointerfaces》2006,50(2):141-146
Previously, novel poly(ethylene glycol) (PEG) and sulfonated PEG acrylate (PEG-SO3A/OA) copolymers were prepared as coating and/or blending materials for biomedical applications. Surfaces modified with copolymers exhibited increased anti-coagulation properties and decreased plasma adsorption level due to increased hydrophilic properties and reorientation characteristics of PEG/PEG-SO3A chains in water phase. As continuation study, anti-complement effects of PEG-SO3/OA copolymers were investigated in vitro, and compared with those of low-density polyethylene (LDPE) and PEG/OA. C3 activation by PEG-SO3/OA samples was lower than that by PEG/OA samples, which was attributed to decreased surface nucleophile level of samples. PEG-SO3/OA samples increased inhibition of Bb production, resulting in decreased C5 activation. Owing to reduced activations of C3 and C5, PEG-SO3/OA samples markedly decreased SC5b-9 levels in plasma. 相似文献
87.
Lee JM Min YJ Lee KB Jeon SG Na JG Ryu HJ 《Langmuir : the ACS journal of surfaces and colloids》2010,26(24):18788-18797
The awareness of symptoms of global warming and its seriousness urges the development of technologies to reduce greenhouse gas emissions. Carbon dioxide (CO(2)) is a representative greenhouse gas, and numerous methods to capture and storage CO(2) have been considered. Recently, the technology to remove high-temperature CO(2) by sorption has received lots of attention. In this study, hydrotalcite, which has been known to have CO(2) sorption capability at high temperature, was impregnated with K(2)CO(3) to enhance CO(2) sorption uptake, and the mechanism of CO(2) sorption enhancement on K(2)CO(3)-promoted hydrotalcite was investigated. Thermogravimetric analysis was used to measure equilibrium CO(2) sorption uptake and to estimate CO(2) sorption kinetics. The analyses based on N(2) gas physisorption, X-ray diffractometry, Fourier transform infrared spectrometry, Raman spectrometry, transmission electron microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy were carried out to elucidate the characteristics of sorbents and the mechanism of enhanced CO(2) sorption. The equilibrium CO(2) sorption uptake on hydrotalcite could be increased up to 10 times by impregnation with K(2)CO(3), and there was an optimal amount of K(2)CO(3) for a maximum equilibrium CO(2) sorption uptake. In the K(2)CO(3)-promoted hydrotalcite, K(2)CO(3) was incorporated without changing the structure of hydrotalcite and it was thermally stabilized, resulting in the enhanced equilibrium CO(2) sorption uptake and fast CO(2) sorption kinetics. 相似文献
88.
Jie Song Eunji Lee Byoung‐Ki Cho 《Journal of polymer science. Part A, Polymer chemistry》2013,51(2):446-456
A well‐defined (PEO‐PS)2‐PLA miktoarm terpolymer ( 1 ) was synthesized by stepwise click reactions of individually prepared poly(ethylene oxide) (PEO), polystyrene (PS, polymerized by atom transfer radical polymerization), and polylactide (PLA, polymerized by ring‐opening polymerization) blocks. As characterized by differential scanning calorimetry and small‐angle X‐ray scattering techniques, the terpolymer self‐assembled into a hexagonal columnar structure consisting of PLA/PEO cylindrical cores surrounded by PS chains. In contrast, the ion‐doped sample ( 1‐Li+ ) with lithium concentration per ethylene oxide = 0.2 exhibited a three‐phase lamellar structure, which was attributed to the microphase separation between PEO and PLA blocks and to the conformational stabilization of the longest PLA chain. The two‐phase columnar morphology before the ion doping was used to prepare a nanoporous material. PLA chains in the cylindrical core region were hydrolyzed by sodium hydroxide, producing nanopores with a pore diameter of about 14 nm. The resulted nanoporous material sank to the bottom in water, because of water‐compatible PEO chains on the walls. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
89.