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81.
Summary Several new dioxouranium(VI) complexes with the tridentate dibasic Schiff bases derived from salicylaldehyde, 5-chloro-, 5-bromo-, 5-nitro-, 3,5-dichloro-, 4-methoxy-, 5-methoxy- and 3-ethoxysalicylaldehyde and 2-hydroxy-1-naphthaldehyde ando-aminobenzyl alcohol, have been synthesized from uranyl acetate dihydrate and the Schiff base in methanol. The complexes are of the type UO2(AAA). MeOH (where AAAH2 = a tridentate dibasic Schiff base). The complexes have been characterized by elemental analyses, i.r. and electronic spectra, conductance, magnetic susceptibility and molecular weight measurements. Thev (U=O) stretching frequency of the complexes occurs atca. 900 cm–1 and the U-O distance is 1.74Å. The complexes are monomers, diamagnetic and octahedral. 相似文献
82.
83.
A convenient solvent‐free one‐pot synthesis of 1,3,5,7‐tetraaryl‐1,3,4,7‐tetrahydro‐2‐thio‐xopyrrolo[2,3‐d]pyrimidin‐4‐one derivatives using supported reagents under microwave irradiation is described. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:617–621, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20355 相似文献
84.
Sham M. Sondhi Monika Johar Nidhi Singhal Sunanda G. Dastidar Rakesh Shukla Ram Raghubir 《Monatshefte für Chemie / Chemical Monthly》2000,7(4):511-520
Various sulfa drugs were condensed with 4-isothiocyanato-4-methyl-2-pentanone at pH∼3–5 by refluxing in methanol to give various substituted mercaptopyrimidines. On condensation with 9-chloro-2-substituted or -unsubstituted acridines, sulfathiazole gave the corresponding condensed products. N-Ethylaminoadenosine reacted with 9-chloroacridine to the coupled product. Condensation of sulfathiazole with 9-isothiocyanato-2,4-substituted or -unsubstituted acridines afforded the corresponding condensed compounds. The structures of all synthesized compounds were confirmed by spectroscopic methods. Anticancer, antiinflammatory, and analgesic activities of all compounds were investigated. 相似文献
85.
86.
Daxesh P. Patel Primal Sharma Mallika Sanyal Puran Singhal Pranav S. Shrivastav 《Biomedical chromatography : BMC》2013,27(8):974-986
An ultra‐performance liquid chromatography–tandem mass spectrometry (UPLC‐MS/MS) method has been developed for the simultaneous determination of carvedilol and its pharmacologically active metabolite 4′‐hydroxyphenyl carvedilol in human plasma using their deuterated internal standards (IS). Samples were prepared by solid‐phase extraction using 100 μL human plasma. Chromatographic separation of analytes was achieved on UPLC C18 (50 × 2.1 mm, 1.7 µm) column using acetonitrile‐4.0 mm ammonium formate, pH 3.0 adjusted with 0.1% formic acid (78:22, v/v) as the mobile phase. The multiple reaction monitoring transitions for both the analytes and IS were monitored in the positive electrospray ionization mode. The method was validated over a concentration range of 0.05–50 ng/mL for carvedilol and 0.01‐10 ng/mL for 4′‐hydroxyphenyl carvedilol. Intra‐ and inter‐batch precision (% CV) and accuracy for the analytes varied from 0.74 to 3.88 and 96.4 to 103.3% respectively. Matrix effect was assessed by post‐column analyte infusion and by calculation of precision values (coefficient of variation) in the measurement of the slope of calibration curves from eight plasma batches. The assay recovery was within 94–99% for both the analytes and IS. The method was successfully applied to support a bioequivalence study of 12.5 mg carvedilol tablets in 34 healthy subjects. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
87.
An improved clean methodology has been developed for the synthesis of pyrido[2,3‐d]pyrimidin‐4‐ones through a simple one‐pot reaction of chalcones, ketones, and ammonium acetates via a [3+2+1] ring annulation. This dry media methodology, where the three components absorbed over solid inorganic support under microwave irradiation, afforded the desired product in a short reaction time. 相似文献
88.
Bhupinder Singh Sumedha Ahuja R. K. Singhal P. Venu Babu 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(1):249-257
The experiment was conducted to determine the effect of gamma radiation on plant growth and development, flag leaf gas exchange characteristics such as net photosynthetic rate (P N), stomatal conductance (g s), and transpiration rate (E) and activity of key carbon and nitrogen assimilating enzymes like Rubisco, starch synthase (SS) and nitrate reductase (NR) in field grown wheat. Grains of cultivar PBW-343 were exposed to a 60Co (Cobalt-60) gamma source at a dose range from 0 to 500 Gy (Gray). Gas exchange characteristics of flag leaf were measured using Infrared Gas Analyzer (IRGA), while mineral nutrients were analyzed spectrophotometrically. Our results show that an irradiation treatment, in general, caused an improvement in plant growth and yield characteristics such as shoot and root mass, root length and surface area, leaf area and chlorophyll SPAD index, tiller number and grain yield. However, irradiation exceeding 5 Gy reduced the magnitude of radiation advantage for most of the investigated physiological and biochemical traits. No germination was recorded at 500 Gy irradiation dose. A dose-dependant increase in shoot Fe in radiated plants up to 25 Gy reflected its higher plant root to shoot translocation which may yield micronutrient rich grains. At higher dose of 100 Gy, there was a drastic reduction in flag leaf membrane stability index (MSI), photosynthesis, Rubisco, NR, and nutrients like K, P, Mg, Fe, and Zn. Starch synthase enzyme activity was unaffected by gamma irradiation indicating that the negative effect of high dose (100 Gy) on the grain yield were caused by the adverse effect of radiation on the gas exchange attributes particularly photosynthesis, carbon, and nitrogen assimilation efficiency and the plant uptake of mineral nutrients. The study concludes that gamma radiation at a low dose (25 Gy or lower) stimulates, while a high dose (100 Gy and above) inhibits plant growth and development of wheat. The adverse effect at 100 Gy and beyond could be attributed to the poor carbon and nitrogen assimilation efficiency and the plant uptake of mineral nutrients, all of which are the ultimate determinant of plant health. 相似文献
89.
R. K. Singhal H. Basu A. V. R. Reddy 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(2):1345-1351
In case of natural catastrophic nuclear accident scenario like Daiichi Nuclear Power Plant (NPP) Fukushima, Japan (11 March 2011) and industrial nuclear accidents like Chernobyl, USSR (March 1986), thousands of curies of activity goes in the public domain and contaminate the drinking water system in the area around the accidental zone. In view of this there is a need to evolve methodology for decontamination of the drinking water without compromising the drinking water quality. During this work humic coated colloidal suspension of geothite(α-FeO(OH)) followed by ultrafiltration were used to decontaminate the water having 239+240Pu and 241Am in the concentration range of 10–100 Bq L?1. Polydispersive colloids of goethite were generated by controlled oxidation of FeSO4 in the presence of NaOH. Size characterization, morphology and elemental profiling of goethite suspension and their aggregation with increase in the concentration of humic acid was studied by using dynamic light scattering and scanning electron microscope hyphenated with energy dispersive spectrometry. Experimental results clearly indicate preferential association of Pu and Am with goethite suspension dominated with 30 nm colloids. The impact of humus material on selectivity of Pu and Am by goethite was studied in the concentration range of 10–100 μg mL?1 of humic acid. This selectivity is further enhanced linearly with the increase in concentration humic acid from 10 to 60 μg mL?1 and thereafter it remains constant. Goethite suspension having a coating of 60 μg mL?1 of humic acid was successfully utilized to decontaminate the water. Goethite suspension was separated from the groundwater using Ultra filtration cell with membrane having 500 NMWL (nominal molecular weight limit). 相似文献
90.
Garima Singhal Riju Bhavesh Kunal Kasariya Ashish Ranjan Sharma Rajendra Pal Singh 《Journal of nanoparticle research》2011,13(7):2981-2988
Development of green nanotechnology is generating interest of researchers toward ecofriendly biosynthesis of nanoparticles.
In this study, biosynthesis of stable silver nanoparticles was done using Tulsi (Ocimum sanctum) leaf extract. These biosynthesized nanoparticles were characterized with the help of UV–vis spectrophotometer, Atomic Absorption
Spectroscopy (AAS), Dynamic light scattering (DLS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR),
and Transmission electron microscopy (TEM). Stability of bioreduced silver nanoparticles was analyzed using UV–vis absorption
spectra, and their antimicrobial activity was screened against both gram-negative and gram-positive microorganisms. It was
observed that O. sanctum leaf extract can reduce silver ions into silver nanoparticles within 8 min of reaction time. Thus, this method can be used
for rapid and ecofriendly biosynthesis of stable silver nanoparticles of size range 4–30 nm possessing antimicrobial activity
suggesting their possible application in medical industry. 相似文献