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931.
Silica–polystyrene core‐shell particles were successfully prepared by surface‐mediated reversible addition fragmentation chain transfer (RAFT) polymerization of styrene monomer from the surfaces of the silica‐supported RAFT agents. Initially, macro‐RAFT agents were synthesized by RAFT polymerization of γ‐methacryloxypropyltrimethoxysilane (MPS) in the presence of chain transfer agents (CTAs). Immobilization of CTAs onto the silica surfaces was then performed by reacting silica with macro‐RAFT agents via a silane coupling. Grafting of polymer onto silica forms core‐shell nanostructures and shows a sharp contrast between silica core and polymer shell in the phase composition. The thickness of grafted‐polymer shell and the diameter of core‐shell particles increase with the increasing ratio of monomer to silica. A control experiment was carried out by conventional free radical emulsion copolymerization of MPS‐grafted silica and styrene under comparable conditions. The resulting data provide further insight into the chemical composition of grafted‐polymers that are grown from the silica surface through RAFT process. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 467–484, 2009  相似文献   
932.
We report the application of reversible addition‐fragmentation chain transfer polymerization using a novel chain transfer agent toward the synthesis of a variety of copolymers containing proline‐derived monomeric units. This methodology enables ready access to a number of polymeric species with narrow molecular weight distributions, reliable functional unit incorporations, and high conversions. The methodology is also a facile approach to novel copolymeric species incorporating amino acids, which possess unique material properties and the potential for further organocatalytic application. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009  相似文献   
933.
A methodology for the synthesis of well‐defined poly(ethylene oxide)‐block‐poly(vinyl alcohol) (PEO‐b‐PVA) and PVA‐b‐PEO‐b‐PVA polymers was reported. Novel xanthate end‐functionalized PEOs were synthesized by a series of end‐group transformations. They were then used to mediate the reversible addition–fragmentation chain transfer polymerization of vinyl acetate to obtain well‐defined poly(ethylene oxide)‐b‐poly(vinyl acetate) (PEO‐b‐PVAc) and PVAc‐b‐PEO‐b‐PVAc. When these block copolymers were directly hydrolyzed in methanol solution of sodium hydroxide, polymers with brown color were obtained, which was due to the formation of conjugated unsaturated aldehyde structures. To circumvent these side reactions, the xanthate groups were removed by adding a primary amine before hydrolysis and the products thus obtained were white powders. The polymers were characterized by gel permeation chromatography, 1H NMR spectroscopy and FT‐IR. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1901–1910, 2009  相似文献   
934.
Ferrocene (Fe(Cp)2) was added to a thermal initiation of reversible addition‐fragmentation chain transfer (RAFT) polymerization of methyl methacrylate (MMA) with 2‐cyanoprop‐2‐yl 1‐dithionaphthalate (CPDN) as the RAFT agent at 115 °C. It was found that the polymerization was greatly promoted after the addition of Fe(Cp)2 while retaining the characteristics of a typical RAFT polymerization. It was proposed that the formation of a redox initiation system, in which the poly(methyl methacrylate) peroxide (PMMAP) generated in situ as the oxidizer and Fe(Cp)2 as the reducer, was possibly the reason for the interesting polymerization phenomenon. Such a redox initiation mechanism was further validated with ascorbic acid (VC) as the reducer instead of Fe(Cp)2. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3607–3615, 2009  相似文献   
935.
936.
The controlled synthesis and characterization of a range of stimuli responsive cationic terpolymers containing varying amounts of N‐isopropylacrylamide (NIPAM), 3‐(methylacryloylamino)propyl trimethylammonium chloride (MAPTAC), and poly(ethylene glycol)monomethyl methacrylate (PEGMA) is presented. The terpolymers were synthesized using reversible addition‐fragmentation chain transfer (RAFT) polymerization. Compositions of the terpolymers determined using 1H NMR were in close agreement to the theoretical values determined from the monomer feed ratios. GPC‐MALLS was used to analyze the molecular weight characteristics of the polymers, which were found to have low polydispersities (Mw/Mn 1.1–1.4). The phase transitions were studied as a function of PEGMA and NIPAM content using temperature controlled 1H NMR and turbidity measurements (UV‐Vis). The relationship between thermal stability and the comonomer ratio of the polymers was measured using thermogravimetric analysis (TGA). Protein interaction studies were performed to determine the suitability of the polymers for biological applications. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4021–4029, 2008  相似文献   
937.
Darvishi and Barati [M.T. Darvishi, A. Barati, Super cubic iterative methods to solve systems of nonlinear equations, Appl. Math. Comput., 2006, 10.1016/j.amc.2006.11.022] derived a Super cubic method from the Adomian decomposition method to solve systems of nonlinear equations. The authors showed that the method is third-order convergent using classical Taylor expansion but the numerical experiments conducted by them showed that the method exhibits super cubic convergence. In the present work, using Ostrowski’s technique based on point of attraction, we show that their method is in fact fourth-order convergent. We also prove the local convergence of another fourth-order method from 3-node quadrature rule using point of attraction.  相似文献   
938.
The water‐soluble gold nanoparticles stabilized by well‐defined comb‐shaped copolymers have been synthesized successfully. The hybrid nanoparticles consist of gold core and poly[poly(ethylene oxide) methyl ether acrylate]‐block‐poly(N‐isopropylacrylamide) [P(A‐MPEO)‐block‐PNIPAM] shell. The water‐soluble comb‐shaped copolymers, P(A‐MPEO)‐block‐PNIPAM with PNIPAM as a handle, were successfully synthesized via a macromonomer technique using reversible addition fragmentation chain transfer (RAFT) polymerization method. The terminal dithioester group of the comb‐shaped copolymer was reduced to a thiol end group forming SH‐terminated copolymers, P(A‐MPEO)‐block‐PNIPAM‐SH. Successively they were used to stabilize gold nanoparticles by the “grafting‐to” approach. The hybrid nanoparticles were characterized by TEM, UV–vis, and HRTEM. Because of the thermosensitive property of PNIPAM in aqueous solution, the comblike copolymer‐tethered gold nanoparticles show a sharp and reversible phase transition at 30 °C in aqueous solution, which was determined by microdifferential scanning calorimetry. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 341–352, 2008  相似文献   
939.
The k nearest neighbor rule (k-NNR) is a well-known nonparametric decision rule in pattern classification. Fuzzy set theory has been widely used to represent the uncertainty of class membership. Several researchers extended conventional k-NNR to fuzzy k-NNR, such as Bezdek et al. [Fuzzy Sets and Systems 18 (1986) 237–256], Keller et al. [IEEE Trans. Syst. Man, and Cybern. 15(4) (1985) 580–585], Béreau and Dubuisson [Fuzzy Sets and Systems 44 (1991) 17–32]. In this paper, we describe a fuzzy generalized k-NN algorithm. This algorithm is a unified approach to a variety of fuzzy k-NNR's. Then we create the strong consistency of posterior risk of the fuzzy generalized NNR.  相似文献   
940.
Summary For estimating the mean of ap-variate normal distribution under a quadratic loss, a class of estimators, known as Stein's estimators, is known to dominate the maximum likelihood estimator (MLE) forp≧3. But, whereas the risk of the MLE has the same value, equal to a constant, for each component, the maximum component risk of Stein's estimator is large for large values ofp. Certain modification of Stein's rule has been proposed in the literature for reducing the maximum component risk. In this paper, a new rule is given for reducing the maximum component risk. The new rule yields larger reduction in the maximum component risk, compared to its competitor.  相似文献   
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