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21.
《Journal of Coordination Chemistry》2012,65(13):1537-1539
The results of a spectrophotometric investigation of the reaction of the biologically active salt 1-benzoylethylpyridinium-4-aldoxime chloride with aquapentacyanoferrate(II) ion are presented. In spite of the presence of two donor sites, only the carbonyl group of the ligand coordinates to the iron centre. Reaction kinetics are consistent with a dissociative mechanism. 相似文献
22.
Rydberg transitions for the interhalogen ICI, are reported in the wavelength region 160-130 nm. 相似文献
23.
Celiprolol-hydrochloride has been determined using benzylorange and forming ion-pair. The absorbance of yellow coloured ion-pair is measured at 401 nm. Unknown concentrations of celiprolol-hydrochloride is calculated by using the calibration graph of the following calibration equation: y = 0.1602 × + 0.0214 The conditional stability constant of the ion-pair at the optimum pH 6.2 and ionic strength 0.05 is found to be 5.63. The method is successfully applied to the determination of celiprolol-hydrochloride in pharmaceutical preparations. 相似文献
24.
《Analytical letters》2012,45(11-12):1289-1296
Abstract A new sensitive and seleactive method for rapid and accurated determination of nitrofarazone is described. The nitrofurazone is reacted with hydroxyl-amine hydrochloride in alkaline medium to give hydroxamic acid which forms the purple violet coloured complex with iron (III), FeCl3, in acidic medium. The nitrofurazone was determined in presence of commonly used drugs and additives. The results obtained by the proposed and B.P. methods were compared. 相似文献
25.
《Analytical letters》2012,45(14):2394-2405
A novel flow injection procedure to determine N-acetylcysteine and captopril in pharmaceutical formulations is proposed. The flow procedure developed was based on oxidation of the analytes by Fe(III) in acidic medium and subsequent reaction of the Fe(II) generated with excess hexacyanoferrate(III) to produce soluble Prussian blue (KFe[Fe(CN)6]) measured at 700 nm. Detection limits of 1.0 × 10?5 mol L?1 and 3.0 × 10?5 mol L?1 for N-acetylcysteine and captopril, respectively, were found. The sample throughput was 70 h?1 for both analytes and the results obtained were in agreement at a 95% confidence level with those obtained using reference methods. 相似文献
26.
《Analytical letters》2012,45(23-24):2207-2220
Abstract A new and highly sensitive method is presented for the spectrophotometric determination of four imidazoline derivatives: antazoline hydrochloride, tolazoline hydrochloride, xylometazoline hydrochloride and naphazoline nitrate. The method is based on the reaction of the corresponding drug base with 2,6 - dichlorophenol -indophenol (DGPIP) in chloroform to give a blue chromogen exhibiting a maximum at 588 - 603nm. The method could be applied for the quantitative determination of the above drugs either pure or in their pharmaceutical preparations (tablets and nasal drops). The results obtained are accurate and have good reproducibility. 相似文献
27.
《Photonics and Nanostructures》2014,12(1):2-8
In this work we describe an ultraviolet subwavelength focusing in plasmonic nanostructures. A system which provides a 20–25 times local field enhancement at a wavelength of 350 nm is proposed. This system represents a metalized V-shaped groove in a surface of a dielectric medium. Subwavelength focusing is achieved by a plasmon wave propagation along the surface of metal film and by the transfer of electromagnetic field through the dielectric medium. The influence of system parameters on a local field enhancement is investigated. A simplified model that allows for determining the geometric parameters of an optimized resonator is proposed. 相似文献
28.
Laurence S. Rothman 《Journal of Quantitative Spectroscopy & Radiative Transfer》2010,111(11):1514-1515
The publication by G.H. Dieke and H.M. Crosswhite (JQSRT 1962;2:97-199) is a classic paper detailing the spectroscopy of the A2Σ+←X2Π bands of the hydroxyl radical (OH) in the ultraviolet region. It soon became the basis of astrophysical modeling, most subsequent theoretical and laboratory studies of the OH individual line parameters, and a host of other applications. 相似文献
29.
A validated spectrophotometric method has been developed for the determination of uranyl ion in soil samples. The method is based on the complexation reaction between uranyl ion and rifampicin in methanol‐water medium at room temperature. The method is followed spectrophotometrically by measuring the absorbance at 375 nm. Under the optimized experimental conditions, Beer's law is obeyed in the concentration range of 1.35–20.25 μg mL‐1 with apparent molar absorptivity and Sandell's sensitivity of 8.0 × 103 L mol‐1cm‐1 and 0.042 μg/cm2/0.001 absorbance unit, respectively. The interference of a large number of anions and cations has been investigated and the optimized conditions developed have been utilized for the determination of uranium(VI) in soil samples. The three sigma detection limit (n = 9) for uranyl ion was found to be 0.20 μg mL‐1. The proposed method was successfully applied to the determination of uranyl ion in soil samples. 相似文献
30.
Abbas Afkhami Tayyebeh Madrakian Saeid Soltanbeygi Majid Rezaeivala 《Journal of Molecular Structure》2011,985(1):86-90
The complex formation between a new synthesized Schiff base and the cations Ni2+, Co2+, Cu2+, Zn2+ in dichloromethane (DCM) and chloroform solutions was investigated spectrophotometrically using rank annihilation factor analysis (RAFA). The results of mole ratio plots and continuous variation data show the stoichiometry of complexation were found to be 1:1, and 2:1 metal ion to ligand. The stoichiometry was obtained as 1:1 metal ion to ligand ratio for Co2+, Ni2+ and Zn2+ in chloroform and 2:1 for Cu2+. In DCM the stoichiometry was obtained as 1:1 for Co2+ and 2:1 for Ni2+ and Zn2+ and a consecutive 2:1 metal ion to ligand ratio was obtained for Cu2+. Formation constants of these complexes were estimated by application of RAFA on spectrophotometric data. In this process the contribution of ligand was removed from the absorbance data matrix when the complex stability constant acts as an optimizing object and simply combined with the pure spectrum of the ligand, the rank of the original data matrix can be reduced by one by annihilating the information of the ligand from the original data matrix. 相似文献