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61.
Mustafa Ç. Pinar 《Mathematical Methods of Operations Research》1996,44(3):345-370
We use quadratic penalty functions along with some recent ideas from linearl
1 estimation to arrive at a new characterization of primal optimal solutions in linear programs. The algorithmic implications of this analysis are studied, and a new, finite penalty algorithm for linear programming is designed. Preliminary computational results are presented.Research supported by grant No. 11-0505 from the Danish Natural Science Research Council SNF. 相似文献
62.
Catalán J Hopf H Mlynek C Klein D Kilickiran P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(13):3915-3920
The absorption, fluorescence and fluorescence excitation spectra for 3,20-di(tert-butyl)-2,2,21,21-tetramethyl-all-trans-3,5,7,9,11,13,15,17,19-docosanonaen (ttbP9) in dilute solutions of 2-methylbutane were recorded at temperatures over the range 120-280 K. The high photostability of this nonaene allows us to assert that it exhibits a single fluorescence and that this can be unequivocally assigned to emission from its 1(1)B(u) excited state, it being the first excited electronic state. Available photophysical data for this polyene and the wealth of information reported for shorter all-trans polyenes allow us to conclude that if the first excited electronic state for the chromophore possessed 2(1)A(g) symmetry, then the energy of such a state might have been so close to that of the 1(1)B(u) state that: 1) the radiationless internal conversion mechanism would preclude the observation of the emission from the 1(1)B(u) state reported in this work and 2) the 2(1)A(g) state reached through internal conversion would be vibrationally coupled to 1(1)B(u) and would facilitate the detection of the emission from 2(1)A(g), which was not observed in any of the solvents used in this work. The spectroscopic and photochemical implications of these findings for other polyenes are discussed. 相似文献
63.
A first order derivative spectrophotometric method has been developed for the simultaneous determination of bismuth and zinc by dithizone without time-consuming extraction step. The reactions of bismuth and zinc with dithizone in a three component solution prepared in water, acetone and n-propanol mixture have been investigated. These cations react with dithizone in this mixture at pH 5.0, forming coloured complex that is stable for at least 2 h. The linear range in D evaluation was between 3.0 × 10−6 and 1.8 × 10−5 mol l−1 for Zn and 2.4 × 10−6 and 1.2 × 10−5 mol l−1 for Bi. The limits of detection for the analytical procedure were found 0.05 mg l−1 for both cations. The relative standard deviations for the determination of 0.5 mg l−1 bismuth and 0.5 mg l−1 zinc were 1.2 and 1.1%, respectively, for five determinations. The procedure is simple, rapid and reliable. This method was applied to the determination of bismuth and zinc in the pharmaceutical materials successfully. Good agreement was achieved between the results obtained by the proposed and comparative methods. 相似文献
64.
Kara P Ozkan D Kerman K Meric B Erdem A Ozsoz M 《Analytical and bioanalytical chemistry》2002,373(8):710-716
The electrochemical behavior of hemin, an iron complex of porphyrin, on binding to DNA at a glassy carbon electrode (GCE) and in solution, is described. Hemin, which interacts with covalently immobilized calf thymus DNA, was detected by use of a bare GCE, a double-stranded DNA-modified GCE (dsDNA-modified GCE), and a single-stranded DNA-modified GCE (ssDNA-modified GCE), in combination with differential pulse voltammetry (DPV). The structural conformation of DNA was determined from changes in the voltammetric signals acquired on reduction of hemin. As a result of its large steric structure and anionic substitution on its porphyrin plane, hemin intercalates between the base pairs of dsDNA. A scan-rate study for hemin and the dsDNA-hemin complex were also performed to determine the electrochemical behavior of the complex. The partition coefficient was obtained from the peak currents measured when different concentrations of hemin were in the presence of dsDNA. By observing the oxidation signals of guanine, damage to DNA after reaction with hemin at the GCE surface was also detected. The electrochemical detection of hybridization between the covalently immobilized probe and its target sequence was detected by use of hemin. These results demonstrate the use of DNA biosensors in conjunction with hemin for electrochemical detection of hybridization and damage to DNA. 相似文献
65.
DNA biosensors based on nucleic acid hybridization processes are rapidly being developed towards the goal of rapid and inexpensive diagnosis of genetic and infectious diseases. Electrochemical transducers are often being used for detecting the DNA hybridization event, due to their high sensitivity, small dimensions, low cost, and compatibility with microfabrication technology. In this study, an electrochemical biosensor for the voltammetric detection of DNA sequences related to the Hepatitis B virus (HBV) and TT virus (TTV) from polymerase chain reaction (PCR) amplified real samples is described for the first time. The biosensor relies on the immobilization of the 21- or 24-mer single stranded oligonucleotides (probe) related to the HBV and TTV sequences and hybridization of these oligonucleotides with their complementary sequences (target) at carbon paste electrode (CPE). The extent of hybridization between the probe and target sequences was determined by using square wave voltammetry (SWV) with moving average baseline correction and methylene blue (MB) as the hybridization indicator. As a result of the interaction between MB and the bound guanine bases of hybrid at CPE surface, the MB signal decreased, when it was compared with the MB signal, which was observed with probe modified CPE. The difference between the MB signals, obtained from the hybrid modified and the probe modified CPE is used to detect the DNA sequences of the infectious diseases from PCR amplified real samples. Numerous factors affecting the target hybridization and indicator binding reactions are optimized to maximize the sensitivity. 相似文献
66.
Optical properties of diluted magnetic semiconductor Ga0.999Mn0.001As/AlAs quantum well structures grown on (1?0?0?), (1?1?0), (3?1?1)B and (4?1?1)B by molecular beam epitaxy are reported. Temperature-dependent spectral photoluminescence (PL) measurement was performed at temperatures between 15 and 300 K. The PL measurements showed that band gap of the alloy decreases with increasing lattice temperature regardless the growth orientations. S-shaped temperature dependence has been observed in the samples grown on (1?0?0), (3?1?1)B, (4?1?1)B orientations. PL emission energy is fitted with Varshni and Bose–Einstein Approximation to determine Debye temperature (β), (ΘE) and thermal expansion coefficient (α), the exciton–phonon coupling strength (aB). 相似文献
67.
F. Belzunce J. F. Pinar J. M. Ruiz 《Annals of the Institute of Statistical Mathematics》2005,57(4):803-815
In this paper we develop a new family of tests for the dilation order based in a characterization of the dilation order. This
family of tests statistics can be used for testing the exponentiality against HNBUE (HNWUE) alternatives. Asymptotic distributional
results are given for both families of tests. For the HNBUE (HNWUE) we also derive the exact distribution under the null hypothesis.
Supported by Ministerio de Ciencia y Tecnologia under Grant BFM2003-02497/MATE.
Supported by Fundación Séneca (CARM). 相似文献
68.
69.
Pinar Sinem Omurtag Ufuk Saim Gunay Aydan Dag Hakan Durmaz Gurkan Hizal Umit Tunca 《Journal of polymer science. Part A, Polymer chemistry》2013,51(10):2252-2259
The Diels‐Alder reaction as a click reaction strategy is applied to the preparation of well‐defined polycarbonate (PC)‐block copolymers. A well‐defined α‐anthracene‐terminated polycarbonate (PC‐anthracene) is prepared using 9‐anthracene methanol as an initiator in the ring opening polymerization of benzyl 5‐methyl‐2‐oxo‐1,3‐dioxane‐5‐carboxylate in CH2Cl2 at room temperature for 5 h. Next, a well‐defined α‐furan protected maleimide‐terminated‐poly(ethylene glycol) (PEG11‐MI or PEG37‐MI), ‐poly(methyl methacrylate) (PMMA26‐MI), and ‐poly(ε‐caprolactone) (PCL27‐MI) were clicked with the PC‐anthracene at reflux temperature of toluene to yield their corresponding PC‐based block copolymers (PC‐b‐PEG, PC‐b‐PMMA, and PC‐b‐PCL). The homopolymer precursors and their block copolymers were characterized by using the GPC, NMR and UV analysis. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献