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691.
Lyakhovetsky YI Pleshkova AP Shilova EA Ponomareva TV Gasanov RG Tumanskii BL Borisov YA Nekrasov YS 《European journal of mass spectrometry (Chichester, England)》2012,18(4):361-376
C(60) was reacted in the ionization chamber of a mass spectrometer under electron impact (EI) with aldehydes, RCHO (R = Ph, p-FC(6)H(4), F(5)C(6), p-MeOC(6)H(4), α-thienyl, o-HOC(6)H(4), o-BrC(6)H(4), m-BrC(6)H(4) and t-Bu), with the transfer of R? radicals and with Me?-transfer from i-PrCHO and t-BuCHO. Paramagnetic fullerene derivatives were stabilized by the addition of the next R? radical or a hydrogen atom, or hydrogen or bromine atom loss. A detailed study showed that the reaction between C(60) and PhCHO occurred via a homolytic mechanism that matches one reported earlier for the reaction with acetone. This suggests the generality of the mechanism for the reactions of fullerenes with other species in ionization chambers under EI at ca 300°C. All aldehydes, except one, had radicals at the carbonyl group which were different from those in the ketones examined earlier in the reactions. This expanded the variety of radicals which can be transferred to fullerenes during reactions in ionization chambers under EI. Due to this and the hydrogen atom at the CO group of aldehydes, some reactions occurred that were not found for the ketones: the formation of cyclic products C(60)COC(6)H(4) and C(60)OC(6)H(4) for PhCHO, o-BrC(6)H(4)CHO and o-HOC(6)H(4)CHO, respectively, and HC(60)Ph for o- and m-BrC(6)H(4)CHO. The reaction with α- formylthiophen gives the first example of transferring an aromatic heterocyclic radical to C(60) in an ionization chamber under EI. C(70) reacted with PhCHO, p-FC(6)H(4)CHO and i- PrCHO similarly to C(60). The results for the reactions of C(60) with PhCHO and with i- PrCHO were compared with those in solution under UV irradiation. Incomplete but reasonable coincidence was found; in both modes, the addition of Ph?, PhCO? and Me? radicals to C(60) occurred, whereas some other products were formed in solution, and the explanation is given as to why this occurred. This conformity supports the hypothesis based on the results of kindred reactions with ketones and organomercurials: the results of EI-initiated homolytic reactions between fullerenes and other compounds in an ionization chamber can predict the reactivity of the fullerenes toward them in solution. 相似文献
692.
Cell-based biohybrid actuators are integrated systems that use biological components including proteins and cells to power material components by converting chemical energy to mechanical energy. The latest progress in cell-based biohybrid actuators has been limited to rigid materials, such as silicon and PDMS, ranging in elastic moduli on the order of mega (10(6)) to giga (10(9)) Pascals. Recent reports in the literature have established a correlation between substrate rigidity and its influence on the contractile behavior of cardiomyocytes (A. J. Engler, C. Carag-Krieger, C. P. Johnson, M. Raab, H. Y. Tang and D. W. Speicher, et al., J. Cell Sci., 2008, 121(Pt 22), 3794-3802, P. Bajaj, X. Tang, T. A. Saif and R. Bashir, J. Biomed. Mater. Res., Part A, 2010, 95(4), 1261-1269). This study explores the fabrication of a more compliant cantilever, similar to that of the native myocardium, with elasticity on the order of kilo (10(3)) Pascals. 3D stereolithographic technology, a layer-by-layer UV polymerizable rapid prototyping system, was used to rapidly fabricate multi-material cantilevers composed of poly(ethylene glycol) diacrylate (PEGDA) and acrylic-PEG-collagen (PC) mixtures. The incorporation of acrylic-PEG-collagen into PEGDA-based materials enhanced cell adhesion, spreading, and organization without altering the ability to vary the elastic modulus through the molecular weight of PEGDA. Cardiomyocytes derived from neonatal rats were seeded on the cantilevers, and the resulting stresses and contractile forces were calculated using finite element simulations validated with classical beam equations. These cantilevers can be used as a mechanical sensor to measure the contractile forces of cardiomyocyte cell sheets, and as an early prototype for the design of optimal cell-based biohybrid actuators. 相似文献
693.
In this report, we present inverted organic solar cells integrating solution-processed aluminum doped zinc oxide (AZO) and trilayer graphene oxide (GO) as an electron selective and anode buffer layers, respectively. The polymers in this inverted architecture are PCDTBT, PBDTTPD and PCBM as an electron donor and acceptor, respectively and the photovoltaic performance were recorded at 300 K under 100 mW/cm2 light intensity. The characteristics of PCDTBT and PBDTTPD-based inverted solar cells were: open-circuit voltages (Voc’s) 0.74 and 0.70 V, short-circuit current densities (Jsc’s) −12.09 and −12.06 mA/cm2, fill factors (FFs) of 60.73% and 60.03%, with an overall power conversion efficiencies (PCEs) of about 5.46% and 5.07%. The fabricated inverted cells show better performances compared to conventional structure reference cells. 相似文献
694.
Resonance energy is one of the criteria to measure aromaticity. The effect of the use of different orbital models is investigated in the calculated resonance energies of cyclic conjugated hydrocarbons within the framework of the ab initio Valence Bond Self-Consistent Field (VBSCF) method. The VB wave function for each system was constructed using a linear combination of the VB structures (spin functions), which closely resemble the Kekulé valence structures, and two types of orbitals, that is, strictly atomic (local) and delocalized atomic (delocal) p-orbitals, were used to describe the π-system. It is found that the Pauling-Wheland's resonance energy with nonorthogonal structures decreases, while the same with orthogonalized structures and the total mean resonance energy (the sum of the weighted off-diagonal contributions in the Hamiltonian matrix of orthogonalized structures) increase when delocal orbitals are used as compared to local p-orbitals. Analysis of the interactions between the different structures of a system shows that the resonance in the 6π electrons conjugated circuits have the largest contributions to the resonance energy. The VBSCF calculations also show that the extra stability of phenanthrene, a kinked benzenoid, as compared to its linear counterpart, anthracene, is a consequence of the resonance in the π-system rather than the H-H interaction in the bay region as suggested previously. Finally, the empirical parameters for the resonance interactions between different 4n+2 or 4n π electrons conjugated circuits, used in Randi?'s conjugated circuits theory or Herdon's semi-emprical VB approach, are quantified. These parameters have to be scaled by the structure coefficients (weights) of the contributing structures. 相似文献
695.
Correlation between catalytic activity and surface ligands of monolayer protected gold nanoparticles
Gold nanoparticles (GNPs) are known to be a very good catalyst. Also, the anchoring of GNPs with stabilizing ligands is essential for surface modification, tuning of size and shapes, and to prevent from aggregation in suspension. But the effect of ligand on the catalytic property of ligand-capped GNP is yet to be explored in detail. In this paper, we perform an in-depth study of effect of ligands on the catalytic activity of monolayer protected GNPs. For this study, a series of different ligand functionalized GNPs in suspension as well as functionalized GNPs' thin film on glass substrate are prepared and used as catalysts in two model reactions, viz. borohydride reduction of 4-nitrophenol and redox reaction between potassium ferricyanide and sodium thiosulfate. The functionalization of GNPs with any ligand reduces its virgin catalytic activity, no matter whether the GNPs are suspended or supported as thin film. An increase in alkyl chain length of alkanethiols and alkylamines ligands and their graft density to the surface of GNP reduces its catalytic activity. Interestingly, the capping of GNPs with 11-mercaptoundecanoic acid and 11-mercaptoundecanol ligands completely destroys its catalytic activity. The effect of anchoring group of ligand molecules on the catalytic activity of ligand-protected GNPs is also discussed. 相似文献
696.
Afzan A Abdullah NR Halim SZ Rashid BA Semail RH Abdullah N Jantan I Muhammad H Ismail Z 《Molecules (Basel, Switzerland)》2012,17(4):4326-4342
Carica papaya L. leaves have been used in ethnomedicine for the treatment of fevers and cancers. Despite its benefits, very few studies on their potential toxicity have been described. The aim of the present study was to characterize the chemical composition of the leaf extract from 'Sekaki' C. papaya cultivar by UPLC-TripleTOF-ESI-MS and to investigate the sub-acute oral toxicity in Sprague Dawley rats at doses of 0.01, 0.14 and 2 g/kg by examining the general behavior, clinical signs, hematological parameters, serum biochemistry and histopathology changes. A total of twelve compounds consisting of one piperidine alkaloid, two organic acids, six malic acid derivatives, and four flavonol glycosides were characterized or tentatively identified in the C. papaya leaf extract. In the sub-acute study, the C. papaya extract did not cause mortality nor were treatment-related changes in body weight, food intake, water level, and hematological parameters observed between treatment and control groups. Some biochemical parameters such as the total protein, HDL-cholesterol, AST, ALT and ALP were elevated in a non-dose dependent manner. Histopathological examination of all organs including liver did not reveal morphological alteration. Other parameters showed non-significant differences between treatment and control groups. The present results suggest that C. papaya leaf extract at a dose up to fourteen times the levels employed in practical use in traditional medicine in Malaysia could be considered safe as a medicinal agent. 相似文献
697.
Background
Sonchus asper (SA) is traditionally used for the treatment of various ailments associated with liver, lungs and kidneys. This study was aimed to investigate the therapeutic potential of nonpolar (hexane, SAHE; ethyl acetate, SAEE and chloroform, SACE) and polar (methanol, SAME) crude extracts of the whole plant. 相似文献698.
Saeed Ahmad Muhammad Nawaz Tahir Hafza Mariyam Javaid Muhammad Monim-ul-Mehboob Muhammad Ashraf Shaheen Rashid Mahmood 《Journal of chemical crystallography》2012,42(4):401-404
Abstract
A cyanido-bridged Cu(II)–Ag(I) bimetallic complex, [Cu(Imidazole)4{Ag(CN)2}2] has been prepared and structurally characterized. The compound crystallizes in the orthorhombic space group Pmna. The crystal structure of the complex consists of trinuclear molecules made up of one [Cu(Imidazole)4]+2 and two [Ag(CN)2]− units. The trinuclear molecules are interlinked to each other through N–H–N and C–H–N hydrogen bonds. The Cu(II) ions are located on mirrors and assume distorted octahedral geometry with the basal plane consisting of four imidazole N-atoms. 相似文献699.
This paper presents a method for coupling isoparametric cubic quadrilateral h-elements and straight sided serendipity quadrilateral p-elements. The p-elements are used to model the interior of the domain while the h-elements are used to describe accurately the curved boundaries. At a common side shared by a p-element and an arbitrary number of h-elements, the field variables are minimized in the least square sense with respect to the degrees-of-freedom of the h-elements. This leads to a set of equations which relate the degrees-of-freedom of the coupled elements on the shared side. The method is applied to the calculation of frequencies for plates with curvilinear plan-forms. The effects of shear deformation and rotary inertia are taken into account. The frequencies are obtained for a sectorial plate with simply supported radial edges and free circular edge, an annular sectorial plate with simply supported radial edges and clamped circular edges, and a circular plate with one concentric ring support. Furthermore, new accurate frequencies are given for a fully clamped square plate with a corner cut-out. Constant meshes are used and convergence is sought by increasing progressively the degree p of the interpolating polynomial. The fast convergence and high accuracy of the method are validated through convergence and comparison studies. 相似文献
700.
Rashid O. Kadara Norman Jenkinson Craig E. Banks 《Electrochemistry communications》2009,11(7):1377-1380
We report the fabrication of disposable and flexible screen printed microelectrodes which are characterised with microscopy and cyclic voltammetry. These new type of screen printed electrochemical platforms consist of micro-sized graphite typically with radii of 60 to 100 microns are defined by an inert dielectric. The advantage of this type of electrochemical sensing platform is that each microelectrode is disposable and cost effective and thus does not require extensive cleaning or electrode pre-treatment between measurements. Prior to measurements the screen printed microelectrode needs only to be calibrated with a suitable redox probe, as is typically the case with microelectrodes. We show proof of concept that the screen printed microelectrodes are advantageous for electro-analytical measurements with the example of determination of lead via cathodic stripping voltammetry. The use of graphite screen printed microelectrodes allows comparable detection limits to that obtained in the literature at insonated boron doped diamond electrodes, without the need for power ultrasound – which otherwise limits the widespread applicability and ease of measurement. 相似文献