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41.
Fleischer JW Carmon T Segev M Efremidis NK Christodoulides DN 《Physical review letters》2003,90(2):023902
We report the first experimental observation of discrete solitons in an array of optically induced waveguides. The waveguide lattice is induced in real time by illuminating a photorefractive crystal with a pair of interfering plane waves. We demonstrate two types of bright discrete solitons: in-phase self-localized states and the staggered (pi out-of-phase) soliton family. This experiment is the first observation of bright staggered solitons in any physical system. Our scheme paves the way for reconfigurable focusing and defocusing photonic lattices where low-power (mW) discrete solitons can be thoroughly investigated. 相似文献
42.
We consider a semilinear heat equation in one space dimension, with a random source at the origin. We study the solution, which describes the equilibrium of this system, and prove that, as the space variable tends to infinity, the solution becomes a.s. asymptotic to a steady state. We also study the fluctuations of the solution around the steady state. 相似文献
43.
Nikos P. Tzanetos Joannis K. Kallitsis 《Journal of polymer science. Part A, Polymer chemistry》2005,43(5):1049-1061
Atom transfer radical polymerization was used to prepare well‐defined vinyl polyoxadiazole homomacromonomers with a properly modified α‐dicarboxylic acid methyl ester as the initiator. Macromonomers of various molecular weights with narrow polydispersities in some cases were obtained, as proved by gel permeation chromatography (GPC). The structures of the obtained macromonomers were then identified with 1H NMR spectroscopy. These macromonomers were subsequently copolymerized with a dihydroxy anthracene based monomer by a polycondensation technique, and this resulted in polymacromonomers. Coil–rod–coil copolymers containing side‐chain anthracene and oxadiazole units were also synthesized by atom transfer radical polymerization. The resulting copolymers combined an anthracene derivative as the rigid block with a random copolymer of the desired anthracene‐ and/or oxadiazole‐based monomers as the flexible block. These copolymers were primarily characterized with GPC and 1H NMR techniques. Additionally, the optical properties of all these copolymers were investigated in detail, and they suggested energy transfer from the oxadiazole to the anthracene chromophores, which became much more efficient in the solid state. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1049–1061, 2005 相似文献
44.
Panagiota Fragouli Hermis Iatrou David J. Lohse Nikos Hadjichristidis 《Journal of polymer science. Part A, Polymer chemistry》2008,46(12):3938-3946
Three linear pentablock quintopolymers (l‐SIDMV), where S is polystyrene (PS), I polyisoprene‐1,4 (PI), D poly(dimethylsiloxane) (PDMS), M poly(tert‐butyl methacrylate) (PtBuM), and V poly(2‐vinylpyridine) (P2VP), were synthesized by anionic polymerization high vacuum techniques. The approach involves the following: (a) The synthesis of living triblock terpolymer PS‐b‐PI‐b‐PDMSLi and diblock copolymer P2VP‐b‐PtBuMK by sequential polymerizations of the corresponding monomers with sec‐BuLi and benzyl potassium, respectively; and (b) The selective linking of the living triblock terpolymer with the chlorosilane group of 2‐(chloromethylphenyl)ethyldimethylchlorosilane (CMPDMS), followed by linking of the living block copolymer with the remaining chloromethyl group of CMPDMS. Molecular characterization carried out by size exclusion chromatography, membrane osmometry, solution (in CDCl3 or d8‐toluene) and solid‐state 1H‐NMR spectroscopy indicated a high degree of molecular and compositional homogeneity. Differential scanning calorimetry results on the precursors and final polymers were discussed. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3938–3946, 2008 相似文献
45.
A. Voros 《Communications in Mathematical Physics》1987,110(3):439-465
The functional determinant of an eigenvalue sequence, as defined by zeta regularization, can be simply evaluated by quadratures. We apply this procedure to the Selberg trace formula for a compact Riemann surface to find a factorization of the Selberg zeta function into two functional determinants, respectively related to the Laplacian on the compact surface itself, and on the sphere. We also apply our formalism to various explicit eigenvalue sequences, reproducing in a simpler way classical results about the gamma function and the BarnesG-function. Concerning the latter, our method explains its connection to the Selberg zeta function and evaluates the related Glaisher-Kinkelin constantA.Member of CNRS 相似文献
46.
47.
Vasilios Kotzabasakis Konstantinos Kostakis Marinos Pitsikalis Nikos Hadjichristidis David J. Lohse Thomas Mavromoustakos Constantinos Potamitis 《Journal of polymer science. Part A, Polymer chemistry》2009,47(17):4314-4325
The Cs‐symmetry hafnium metallocene [(p‐Et3Si)C6H4]2C(2,7‐di‐tert‐BuFlu)(C5H4)Hf(CH3)2 and tetrakis(pentafluorophenyl) borate dimethylanilinium salt ([B(C6F5)4]?[Me2NHPh]+) were used as the catalytic system for the polymerization of higher α‐olefins (from hexene‐1 to hexadecene‐1) in toluene at 0 °C. The evolution of the polymerization was studied regarding the variation of the molecular weight, molecular weight distribution and yield with time. The effect of the monomer structure on the polymerization kinetics was established. The role of trioctylaluminum in accelerating the polymerization was investigated. 13C NMR spectroscopy was used to study the microstructure of the poly(α‐olefins) by the determination of the pentad monomer sequences. The thermal properties of the polymers were obtained by differential scanning calorimetry, DSC. The results were discussed in connection with the polymer microstructure. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4314–4325, 2009 相似文献
48.
Nikos G. Tsierkezos Athanassios I. Philippopoulos Uwe Ritter 《Journal of solution chemistry》2010,39(6):897-908
Cyclic voltammetric studies (CV) on the complex cis-bis(2,2′-bipyridine)bis(thiocyanate)chromium(III) iodide [Cr(bipy)2(SCN)2]I (where bipy: 2,2′-bipyridine, C10H8N2) were recorded on platinum (Pt) and glassy carbon (GC) electrodes in either acetonitrile (ACN) or acetone (ACE) solvent media
including n-tetrabutylammonium hexafluorophosphate (NBu4PF6) as supporting electrolyte, at scan rates (v) ranging from 0.05 to 0.12 V⋅s−1. In addition, electrochemical impedance spectroscopic (EIS) measurements in the frequency (f) range from 0.1 Hz to 50 kHz were carried out on GC and Pt electrodes. The half-wave potential (E
1/2) of the redox couple Cr(III)/Cr(II) was determined as −0.84 V and −0.79 V (versus Ag/AgCl) in ACN and ACE, respectively.
The heterogeneous electron transfer rate constant (k
s) corresponding to the couple Cr(III)/Cr(II) was found to be greater on GC compared to the Pt electrode. The nature of the
solvent medium also affects the kinetics of the investigated couple, to be exact, k
s increases remarkably upon replacement of ACE by ACN. The EIS results indicate that the GC electrode is a better capacitor
and provides the smaller charge transfer resistance in ACN. 相似文献
49.
Gareth P. Keeley Niall McEvoy Shishir Kumar Nikos Peltekis Marcel Mausser Georg S. Duesberg 《Electrochemistry communications》2010,12(8):1034-1036
This communication describes the electrochemical properties of thin pyrolytic carbon (PyC) films created using a reliable, non-catalytic chemical vapour deposition (CVD) process. After deposition, the electron transfer characteristics of the films are optimised using a simple oxygen plasma treatment. The redox probes Ru(NH3)63+/2+, Fe(CN)63?/4? and Fe3+/2+ are employed to demonstrate that the resulting material is endowed with a large electrochemical surface area and outstanding electron transfer properties. Atomic force microscopy (AFM), Raman and X-ray photoelectron spectroscopy (XPS) are used to elucidate the morphology and chemical composition of the electrode surfaces. This material represents a new class of carbon electrode, and its large densities of edge-plane sites and oxygenated functionalities make it an ideal candidate for electrochemical sensor applications. 相似文献
50.
Quantum dots (QDs) are inorganic semiconductor nanocrystals that have unique optoelectronic properties responsible for bringing
together multidisciplinary research to impel their potential bioanalytical applications. In recent years, the many remarkable
optical properties of QDs have been combined with the ability to make them increasingly biocompatible and specific to the
target. With this great development, QDs hold particular promise as the next generation of fluorescent probes. This review
describes the developments in functionalizing QDs making use of different bioconjugation and capping approaches. The progress
offered by QDs is evidenced by examples on QD-based biosensing, biolabeling, and delivery of therapeutic agents. In the near
future, QD technology still faces some challenges towards the envisioned broad bioanalytical purposes.
相似文献