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71.
With a view to understanding the role of photo-induced valence changes of impurities in BaTiO3 in the phenomena of photorefraction, EPR experiments were conducted under in situ He-Ne laser illumination. These experiments gave evidence for photoinduced valence change of Fe in BaTiO3 at room temperature. The EPR signal due to trivalent iron was found to reduce in intensity with laser illumination The kinetics
of the valence change has been investigated. Under large fringe width condition, the time constant of the decay is identified
as the dielectric relaxation time τd. The changes in line shape on laser illumination to Dysonian form, appeared most predominantly in mechanically poled crystal
compared to electrically poled single domain crystals. This demonstrated the possible role of domain walls and the defects
there, as source or sinks of charge carriers on photo excitation. It is observed, that there is transient growth of Fe3+, when the laser illumination was put on, before its decay. This was attributed to charge transfer between electrons in oxygen
vacancies and Fe4+. This predicted the growth of a transient grating under depleted pump condition in a two beam coupling experiment. This was
experimentally proved by following the diffracted signal of the reading beam under the depleted pump condition. 相似文献
72.
G A V Ramanamurthy K Ramachandra Rao Y Rama Krishna P Venkateswarlu K Bhaskara Rao P V Ramana Rao S Venkata Ratnam V Seshagiri Rao G J Nagaraju S Bhuloka Reddy 《Pramana》2001,56(5):697-703
The Measurement of K
β
K
/α
intensity ratios are measured in some 3d shell elements by using a 2 MeV proton beam along with a high resolution Si(Li) detector. The present Measurement of K
β
K
/α
intensity ratios are in good agreement with Scofield modified theoretical values, thus supporting the basic assumptions in
that theory. From the present Measurement of K
β
K
/α
intensity ratios, it is evident that due to chemical effects, the experimental Measurement of K
β
K
/α
intensity ratios will be increased while they will be decreased due to the presence of simultaneous M-shell vacancies which are produced due to proton excitation. 相似文献
73.
Venkateswarlu Chimaladenne Ramesh Manda Ashok Reddy Gudipally Krishna Reddy Valluru Pradeep Kumar Brahman 《合成通讯》2020,50(19):2941-2949
Abstract A mild and efficient base promoted, microwave assisted, green synthesis of 2-amino-2-ene-1,4-diones has been described by the decomposition of phenacyl azides followed by treatment with pyridinium salts of phenacyl bromides in aqueous media. A diverse range of substrates bearing electron-releasing and electron-withdrawing substituents were well tolerated and delivered corresponding 2-amino-2-ene-1,4-diones in good yields. Synthesized 2-amino-2-ene-1,4-diones have been further explored in the synthesis of various substituted 4-hydroxypyrrolidin-2-ones. 相似文献
74.
Epoxides and aziridines are cleaved efficiently and regioselectively in the presence of zirconyl nitrate at room temperature to afford the corresponding β-nitrato-alcohols and -sulfonamides, respectively, in high yields. 相似文献
75.
Panchagnula V Kumar CV Rusling JF 《Journal of the American Chemical Society》2002,124(42):12515-12521
Cross-linking of myoglobin (Mb) promoted by 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide within films of polystyrene sulfonate after layer-by-layer self-assembly provided remarkable stabilization. Cross-linking greatly improved adhesion of the films to fused silica slides and allowed extensive optical studies over a wide pH range. Circular dichroism and visible absorbance spectra showed that Mb retained its native conformation when films were placed in solutions of pH as low as 2 and up to pH 11. Linear dichroism revealed an average orientation of the Mb iron heme cofactors of 58 degrees to the film normal. High concentrations of urea did denature the protein in the films, however. At pH 1, Mb in solution is fully unfolded but retained considerable alpha-helical content in the cross-linked films. Both the polyion film environment and cross-linking seem to play roles in stabilizing protein secondary structure and function at low pH. Cross-linked myoglobin-polyion films on pyrolytic graphite electrodes were used in strongly acidic solutions for the electrochemical catalytic reduction of trichloracetic acid, hydrogen peroxide, and oxygen. The pH-dependent catalytic reduction of trichloracetic acid was faster in 0.1 M HCl than in the medium pH range. 相似文献
76.
A simple and rapid gradient elution high-performance liquid chromatographic method using photodiode array and electrospray ionization mass spectrometric detectors was developed for separation and determination of the process-related substances and photodegradation products of stilbenesulfonic acids, viz. 4,4'-dinitrostilbene-2,2'-disulfonic acid (DNSDA), 4-amino-4'-nitrostilbene-2,2'-disulfonic acid (ANSDA), and 4,4'-diaminostilbene-2,2'-disulfonic acid (DASDA) in industrial waste waters. Gradient elution was carried out using ammonium acetate and acetonitrile as mobile phase and an Inertsil-ODS 3V column for separation. The negative-ion electrospray ionization mass spectra containing [M-H]- ions of sulfonic acids allowed molecular mass determination of unknowns and the structures were proposed on the basis of the fragment ions in the MS/MS spectra. 相似文献
77.
Jaswanth Kumar Inamadugu Rajasekhar Damaramadugu Ramesh Mullangi Venkateswarlu Ponneri 《Biomedical chromatography : BMC》2010,24(10):1059-1074
An LC‐MS/MS method for the simultaneous quantitation of niacin (NA) and its metabolites, i.e. nicotinamide (NAM), nicotinuric acid (NUA) and N‐methyl‐2‐pyridone‐5‐carboxamide (2‐Pyr), in human plasma (1 mL) was developed and validated using nevirapine as an internal standard (IS). Extraction of the NA and its metabolites along with the IS from human plasma was accomplished using a simple liquid–liquid extraction. The chromatographic separation of NA, NAM, NUA, 2‐Pyr and IS was achieved on a Hypersil‐BDS column (150 ¥ 4.6 mm, 5 mm) column using a mobile phase consisting of 0.1% formic acid : acetonitrile (20:80 v/v) at a flow rate of 1 mL/min. The total run time of analysis was 2 min and elution of NA, NAM, NUA, 2‐Pyr and IS occurred at 1.37, 1.46, 1.40, 1.06 and 1.27 min, respectively. A detailed validation of the method was performed as per the FDA guidelines and the standard curves were found to be linear in the range of 100–20000 ng/mL for NA; 10–1600 ng/mL for NUA and NAM and 50–5000 ng/mL for 2‐Pyr with mean correlation coefficient of ≥0.99 for each analyte. The method was sensitive, specific, precise, accurate and suitable for bioequivalence and pharmacokinetic studies. The developed assay method was successfully applied to a pharmacokinetic study in humans. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
78.
K. C. Rajanna M. Venkateswarlu M. Satish Kumar U. Umesh Kumar G. Venkateshwarlu P. K. Saiprakash 《国际化学动力学杂志》2013,45(2):69-80
Vilsmeier–Haack (VH) benzoylation reactions with benzaldehydes and acetophenones in acetonitrile medium obeyed second‐order reaction kinetics. Under kinetic conditions, the reactions afforded benzoyl derivatives irrespective of the nature of oxychloride (POCl3 or SOCl2) used for the preparation of VH reagent along with benzamide. The present finding is advantageous to understand the nature of reactive species as well as the mechanism of benzoylation. © 2012 Wiley Periodicals, Inc. Int J Chem Kinet 45: 69–80, 2013 相似文献
79.
Jaswanth Kumar Inamadugu Rajasekhar Damaramadugu Ramesh Mullangi Venkateswarlu Ponneri 《Biomedical chromatography : BMC》2010,24(9):1006-1014
A simple, sensitive and rapid method has been developed and validated for determination of the metoclopramide (MCP) in 100 μL human plasma. The analytical procedure involves a liquid–liquid extraction method using tramadol as an internal standard (IS). Chromatographic separation was carried out on a HyPURITY ADVANCE column using a mobile phase consisting of acetonitrile and 10 mm ammonium acetate buffer in the ratio of 80:20 (v/v) at a flow rate of 0.3 mL/min. The total run time of analysis was 2.5 min and elution of MCP and IS occurred at 0.9 and 1.3 min, respectively. A linear response function was established for the range of concentrations 0.53–42.07 ng/mL (r > 0.99). The intra‐ and inter‐day precision values for MCP met the acceptance as per FDA guidelines. MCP was stable in a battery of stability studies viz., bench‐top, auto‐sampler and freeze–thaw cycles. The developed assay method was successfully applied to an oral bioequivalence study in humans. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
80.
Proceedings - Mathematical Sciences - The addition of cyanoacetamide to the double bond of 7-methoxy and 7-hydroxycoumarins is very slow and it is attributed to the influence of the substituents... 相似文献