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61.
This paper presents experimental results concerning the influence of the additives on the physical properties of polymer films. Metal oxides/inorganic salts were used as additives in vinyl-polymers solutions. The physical properties of the metal doped polymer films can be significantly modified by the composition of the doping elements and the curing conditions of the polymer. Morphologic, electronic, magnetic and optic properties of the doped polymers were analysed by AFM, SEM, Mössbauer spectroscopy and optical measurements. The film composition and the deposition processes were optimized to allow a better control of the optical parameters (refractive index, transmission), to reduce the processing temperatures and to improve the chemical sensitivity of the films for sensor applications. These compounds can be easily spin coated onto a variety of directly patterned semiconductor substrates.  相似文献   
62.
Polymers consisting of poly(heterocyclic methacrylate)s are considered as potential materials for clinical applications such as drug delivery and cartilage repair. Much of the success of these systems has been attributed to the complex nature of their water sorption properties. Dielectric permittivity is very sensitive to water sorption. Dielectric relaxation spectroscopy studies have been carried out on two heterocyclic poly(methacrylate)s: poly(tetrahydrofurfuryl methacrylate) (PTHFMA) and poly(3‐methyl tetrahydrofurfuryl methacrylate) (P3MTHFMA). The isochrones representing the dielectric losses show in both cases high conductivity at low frequencies and high temperatures. In PTHFMA two conductive processes are observed, which can be associated to the existence of two types of water sorption. These effects have been analyzed and were removed from the dielectric spectra by using classical empirical equations. Both polymers show ostensible α‐relaxation centered in the vicinity of 350 K at 100 Hz. This relaxation was analyzed by means of the empirical Havriliak‐Negami equation. Reminiscent β‐relaxation could also exist. Both polymers present well defined γ and δ subglass absorptions at approximately 120 K, 160 K for PTHFMA and 125 K, 163 K for P3MTHFMA, at 100 Hz, associated to local intramolecular relaxations in side groups. These relaxations were analyzed using semiempirical symmetric model. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 109–120, 2008  相似文献   
63.
We examine a generalization of the binomial distribution associated with a strictly increasing sequence of numbers and we prove its Poisson-like limit. Such generalizations might be found in quantum optics with imperfect detection. We discuss under which conditions this distribution can have a probabilistic interpretation.  相似文献   
64.
In this work, we present a new electrochemical disposable platform based on poly(aniline‐co‐anthranilic acid) (PANI/PAA) composite polymer coupled with an aptamer for sensitive detection of β‐lactoglobulin. Firstly, PANI/PAA film was electrodeposited on the graphite screen‐printed electrode surface by cyclic voltammetry. The co‐polymer modified electrode was then employed as platform for the covalent immobilization of an amino‐modified aptamer. Various β‐lactoglobulin solutions, with a fixed amount of biotinylated oligonucleotide complementary sequence, were dropped onto the aptasensor surface. A streptavidin‐alkaline phosphatase conjugate was then employed to trace the affinity reaction. After the addition of 1‐naphthyl‐phosphate enzymatic substrate, 1‐naphthol electroactive product was detected by differential pulse voltammetry. A decrease in the signal was obtained when the target concentration was increased, in according to a signal‐off approach. After optimization of key experimental parameters, a dose‐response curve was obtained between 0.01–1.0 μg mL?1 β‐lactoglobulin concentration range. The limit of detection of 0.053 μg L?1 was obtained. Milk samples spiked with β‐lactoglobulin were analyzed.  相似文献   
65.
66.
Phosphosilicate glasses are of great interest in important fields, such as optical active systems, energy generating systems, humidity sensors, and as materials for biomedical applications. Many studies were accomplished to establish the influence of different reaction parameters on the evolution and final structure of sol–gel prepared phosphosilicate gels. In the present work, we studied the thermal behavior of the silicophosphate gels obtained starting with different phosphorous precursors, the influence of these precursors on the composition and structure of the resultant gels, and their evolution with thermal treatment. By Fourier transform infrared spectroscopy (FT-IR), thermogravimetric and thermodifferential analysis (DTA/TG), and Differential Scanning calorimetry coupled with Mass Spectrometry (DSC-MS), it was established that the type of the precursors essentially influences the composition and structure and consequently the thermal behavior of the obtained gels. In the case of triethylphosphate precursor, all used methods of investigation have shown that the ester is trapped in the silica matrix and it is eliminated during the thermal treatment. Triethylphosphite partially hydrolizes and reacts with the silica network during post-preparation thermal treatment. Only in the case of H3PO4, an interaction with TEOS takes place and leads to Si–O–P bond formation. By thermal treatment, the gels with different composition and structure lead to materials with different properties.  相似文献   
67.
The title compound, C17H13NO4, crystallizes in two polymorphic forms, each with two molecules in the asymmetric unit and in the monoclinic space group P21/c. All of the molecules have intramolecular hydrogen bonds involving the amide group. The amide N atoms act as donors to the carbonyl group of the pyrone and also to the methoxy group of the benzene ring. The carbonyl O atom of the amide group acts as an acceptor of the β and β′ C atoms belonging to the aromatic rings. These intramolecular hydrogen bonds have a profound effect on the molecular conformation. In one polymorph, the molecules in the asymmetric unit are linked to form dimers by weak C—H...O interactions. In the other, the molecules in the asymmetric unit are linked by a single weak C—H...O hydrogen bond. Two of these units are linked to form centrosymmetric tetramers by a second weak C—H...O interaction. Further interactions of this type link the molecules into chains, so forming a three‐dimensional network. These interactions in both polymorphs are supplemented by π–π interactions between the chromone rings and between the chromone and methoxyphenyl rings.  相似文献   
68.
The molecular conformations of three N‐alkyl‐2‐(methylsulfanyl)nicotinamide derivatives, namely N‐cyclohexyl‐2‐(methylsulfanyl)nicotinamide, C13H18N2OS, (I), N‐isopropyl‐2‐(methylsulfanyl)nicotinamide, C10H14N2OS, (II), in which there are two molecules in the asymmetric unit which were chosen to form a hydrogen‐bonded pair, and N‐(2‐hydroxyethyl)‐2‐(methylsulfanyl)nicotinamide dihydrate, C9H12N2O2S·2H2O, (III), are compared with those of four unsubstituted N‐alkylnicotinamide compounds. The substituted compounds show a higher degree of torsion of the pyridine ring with respect to the amide group than do the unsubstituted compounds, with dihedral angles in the range 40–60° for the former and 20–35° for the latter. In (I) and (II), the supramolecular structure is defined by amide‐N to carbonyl‐O chains. In (III), the nicotinamide molecules are linked by hydrogen bonds to two water molecules resulting in two linked chains of rings which form the three‐dimensional network.  相似文献   
69.
(E)‐2‐(2‐Benzylidenehydrazinylidene)quinoxaline, C15H12N4, crystallized with two molecules in the asymmetric unit. The structures of six halogen derivatives of this compound were also investigated: (E)‐2‐[2‐(2‐chlorobenzylidene)hydrazinylidene]quinoxaline, C15H11ClN4; (E)‐2‐[2‐(3‐chlorobenzylidene)hydrazinylidene]quinoxaline, C15H11ClN4; (E)‐2‐[2‐(4‐chlorobenzylidene)hydrazinylidene]quinoxaline, C15H11ClN4; (E)‐2‐[2‐(2‐bromobenzylidene)hydrazinylidene]quinoxaline, C15H11BrN4; (E)‐2‐[2‐(3‐bromobenzylidene)hydrazinylidene]quinoxaline, C15H11BrN4; (E)‐2‐[2‐(4‐bromobenzylidene)hydrazinylidene]quinoxaline, C15H11BrN4. The 3‐Cl and 3‐Br compounds are isomorphous, as are the 4‐Cl and 4‐Br compounds. In all of these compounds, it was found that the supramolecular structures are governed by similar predominant patterns, viz. strong intermolecular N—H...N(pyrazine) hydrogen bonds supplemented by weak C—H...N(pyrazine) hydrogen‐bond interactions in the 2‐ and 3‐halo compounds and by C—H...Cl/Br interactions in the 4‐halo compounds. In all compounds, there are π–π stacking interactions.  相似文献   
70.
In this paper, the tangential and normal discontinuities at the interface between the scatterer and the matrix are independently modeled, and these relative displacements are directly proportional to the corresponding components of tractions at the interface. The generation of full band-gaps is investigated on the basis of the derived imperfect interface conditions for a sonic plate with an array of acoustic piezoceramic hollow spheres scatterers embedded in an epoxy matrix. The scatterers are made from functionally graded materials with radial polarization. Numerical evaluation has shown that imperfect interface may have a significant effect on the increasing of the length of the full band-gaps. (© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
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