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排序方式: 共有353条查询结果,搜索用时 234 毫秒
41.
R. Albrecht T. C. Awes P. Beckmann F. Berger M. A. Bloomer D. Bock R. Bock G. Claesson G. Clewing L. Dragon A. Eklund R. L. Ferguson A. Franz S. Garpman R. Glasow H. Å. Gustafsson H. H. Gutbrod M. Hartig G. Hölker J. Idh P. Jacobs K. H. Kampert B. W. Kolb P. Kristiansson H. Löhner I. Lund F. E. Obenshain A. Oskarsson I. Otterlund T. Peitzmann S. Persson F. Plasil A. M. Poskanzer M. Purschke H. G. Ritter B. Roters S. Saini R. Santo H. R. Schmidt R. Schmidt S. P. Sørensen K. Steffens P. Steinhauser E. Stenlund D. Stüken M. L. Tincknell A. Twyhues G. R. Young 《Zeitschrift fur Physik C Particles and Fields》1992,53(2):225-237
Correlations between positive pions are investigated in the target fragmentation region of 200A GeV16O+nucleus collisions. The pions are measured with the Plastic Ball detector in the WA80 experiment at the CERN SPS. The target mass dependence of the radii and the correlation strength extracted by interferometry is studied. A new approach to the fit of the correlation function is introduced. The correlation strength and both invariant and transverse radii increase with decreasing target mass. The transverse radius for16O+C reactions appears to be much larger than the geometrical radius of the nuclei involved. For the Au target only a small fraction of the measured pions contributes to the apparent correlation. Hints for a much larger second component in16O+Au reactions are observed. Rescattering phenomena may provide a clue to understand these phenomena. 相似文献
42.
A Convenient and Facile Synthesis of Isoxazolyl‐chromeno[4,3,2‐de]pyrimido[4,5‐h][1,6]napthyridinones
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Eligeti Rajanarendar Saini Ramakrishna Baireddy Kishore 《Journal of heterocyclic chemistry》2014,51(5):1415-1420
The ceric ammonium nitrate‐catalyzed synthesis of (E)‐5‐amino‐N‐(3‐methyl‐5‐styrylisoxazol‐4‐yl)‐2‐arylchromeno[4,3,2‐de][1,6]napthyridin‐4‐carboxamides 5 was simply achieved upon the one‐pot four‐component reaction of isoxazolyl cyanoacetamide 1 with malononitrile 2 , 2‐hydroxy acetophenone 3 , and aromatic aldehydes 4 in ethanol. Compounds 5 on heating with acetic anhydride underwent tandem N‐acetylation and cyclocondensation involving intramolecular cyclization to afford the title compounds (E)‐11‐methyl‐12‐(3‐methyl‐5‐styrylisoxazol‐4‐yl)‐2‐arylchromeno[4,3,2‐de][1,6]napthyridin‐13(12H)‐ones 6 in good yields. The chemical structures have been confirmed by analytical and spectral analyses. 相似文献
43.
44.
Indra Sandal Amita Bhattacharya Uksha Saini Devinder Kaur Shveta Sharma Ashu Gulati Jonnala K Kumar Neeraj Kumar Jyotsna Dayma Pralay Das Bikram Singh Paramvir S Ahuja 《BMC chemical biology》2011,11(1):1-13
Background
Accidental autoclaving of L-glutamine was found to facilitate the Agrobacterium infection of a non host plant like tea in an earlier study. In the present communication, we elucidate the structural changes in L-glutamine due to autoclaving and also confirm the role of heat transformed L-glutamine in Agrobacterium mediated genetic transformation of host/non host plants.Results
When autoclaved at 121°C and 15 psi for 20 or 40 min, L-glutamine was structurally modified into 5-oxo proline and 3-amino glutarimide (α-amino glutarimide), respectively. Of the two autoclaved products, only α-amino glutarimide facilitated Agrobacterium infection of a number of resistant to susceptible plants. However, the compound did not have any vir gene inducing property.Conclusions
We report a one pot autoclave process for the synthesis of 5-oxo proline and α-amino glutarimide from L-glutamine. Xenobiotic detoxifying property of α-amino glutarimide is also proposed. 相似文献45.
Background
Pentachloronitrobenzene (PCNB) and hexachlorobenzene (HCB) are highly toxic and widespread in every environmental compartment. Some of metabolic products such as amino/nitro containing chlorinated aromatic compounds can be determined by gas chromatography coupled with electron capture detector (GC-ECD). However, it is difficult to identify some of chlorophenolic and chloroquinolic intermediates produced from PCNB and HCB by the above mentioned technique. Therefore, for analysis of these compounds and their metabolites, we have developed a high performance liquid chromatography (HPLC) based method.Results
The extraction of PCNB and HCB from soil and minimal salt medium was carried out with ethyl acetate and hexane respectively with good recoveries (98% for PCNB and 97% for HCB). The validation of the proposed extraction and HPLC method was done by analysis of PCNB and HCB biodegradation and their metabolites identification from anaerobic enriched soil samples.Conclusion
A rapid, sensitive and simple HPLC based analytical method was developed for the analysis of PCNB, HCB and their possible intermediates. 相似文献46.
G. Campi E. Cappelluti Th. Proffen X. Qiu E. S. Bozin S. J.L. Billinge S. Agrestini N. L. Saini A. Bianconi 《The European Physical Journal B - Condensed Matter and Complex Systems》2006,52(1):15-21
We have studied temperature evolution of the local as well as the
average crystal structure of MgB2 using real-space atomic pair
distribution function (PDF) measured by high resolution neutron powder
diffraction in a wide temperature range of T=10–600 K. We find small
positive correlation factors for the B–B and B–Mg pairs, determined by
mean-square displacements (MSD) and the mean-square relative
displacements (MSRD). We analyze the PDF using both Einstein and
force constant models finding a good agreement between the
experimental data and the two models. This indicates that B and Mg
atomic correlations are not sensitive to the details of phonon
dispersion. 相似文献
47.
A S Saini 《Journal of chromatography. A》1971,61(2):378-381
48.
Kinetic investigations on the reaction between U(IV) and H2O2 have been carried out at different acidities in chloride medium at an ionic strength of 2M. The observed bimolecular rate constant has been found to be dependant on [H+]?1.3. The activation energy of the overall reaction has been found to vary from 13.4 ± 0.7 to 18.0 ± 0.8 kcal/mol in the range of acidity from 0.3 to 1.5M. The results have been explained on the basis of three parallel rate-controlling reactions involving unhydrolyzed species of U(IV) and hydrolyzed species UCl(OH)2+ and UO2+. The values of the rate constants for these three reaction paths have been found to be of the order of 3.95, 5.59 × 103, and 1.49 × 105M?1 min?1, respectively. 相似文献
49.
The total (p, n) reaction cross section for48Ca has been measured as a function of proton energy in the energy range 1.885 to 5.100 MeV with an overall resolution of ∼
2 keV and in ∼ 5 keV energy steps. The fluctutions in fine resolution data have been analysed to determine the average coherence
width 〈Γ〉. The excitation function averaged over large energy intervals has been analyzed in terms of the optical model. The
isobaric analogue resonances atE
p
∼ 1.95 and 4 MeV have been shape-analyzed to extract the proton partial width and the spectroscopic factorS
n
. A comparison of the gross structures observed in ∼ 55 keV averaged excitation function with the predictions of Izumo’s partial
equilibrium model has also been made. 相似文献
50.
Il Nuovo Cimento D - The temperature dependence of local Cu site conformations in single-domain crystals of Bi2Sr2CaCu2O8+y (Bi-2212) and La1.85Sr0.15CuO4 (La-214) has been determined by EXAFS... 相似文献