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排序方式: 共有101条查询结果,搜索用时 15 毫秒
1.
De Salvo G Gattuso G Notti A Parisi MF Pappalardo S 《The Journal of organic chemistry》2002,67(3):684-692
A series of tri-O-substituted 1,3-bridged calix[5]arene crown-6 ethers bearing alkyl, arylalkyl, alkoxyalkyl, and alkoxycarbonylmethyl residues at the lower rim and either (t)()Bu or H substituents at the upper rim have been synthesized. (1)H NMR studies have shown that p-tert-butylcalix[5]crowns, irrespective of the size and nature of their lower rim pendant groups, adopt preorganized conelike conformations, whereas p-H-calix[5]crowns with bulky substituents preferentially exist in solution as partial cone conformers (C(1) symmetry). Calix[5]crown derivatives behave as mono- or ditopic receptors for isomeric butylammonium ions, forming endo-cavity (inside the calixarene cup) and/or exo-cavity (at the crown ether moiety) 1:1 complexes according to the shape of the guest. These two binding modes can be clearly distinguished and monitored by (1)H NMR titration experiments. 相似文献
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The preparation and physical properties of the layered VS2, MyV1?yS2 (M = Fe or Cr), and their lithium intercalation adducts are described. These compounds were prepared by oxidative delithiation of LiMyV1?yS2 with iodine. Crystallographic distortions present in LixVS2 (0.25 ? x ? 0.6) are suppressed by Fe or Cr substitution for V. The electrochemical sluggishness of Li/Li+/VS2 cells is reduced by the substitution. 相似文献
4.
Laveissière G Todor L Degrande N Jaminion S Jutier C Di Salvo R Van Hoorebeke L Alexa LC Anderson BD Aniol KA Arundell K Audit G Auerbach L Baker FT Baylac M Berthot J Bertin PY Bertozzi W Bimbot L Boeglin WU Brash EJ Breton V Breuer H Burtin E Calarco JR Cardman LS Cavata C Chang CC Chen JP Chudakov E Cisbani E Dale DS de Jager CW De Leo R Deur A d'Hose N Dodge GE Domingo JJ Elouadrhiri L Epstein MB Ewell LA Finn JM Fissum KG Fonvieille H Fournier G Frois B Frullani S Furget C Gao H Gao J 《Physical review letters》2004,93(12):122001
We report a virtual Compton scattering study of the proton at low c.m. energies. We have determined the structure functions P(LL)-P(TT)/epsilon and P(LT), and the electric and magnetic generalized polarizabilities (GPs) alpha(E)(Q2) and beta(M)(Q2) at momentum transfer Q(2)=0.92 and 1.76 GeV2. The electric GP shows a strong falloff with Q2, and its global behavior does not follow a simple dipole form. The magnetic GP shows a rise and then a falloff; this can be interpreted as the dominance of a long-distance diamagnetic pion cloud at low Q2, compensated at higher Q2 by a paramagnetic contribution from piN intermediate states. 相似文献
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Catalytic ignition of ionic liquids for propellant applications 总被引:1,自引:0,他引:1
Shamshina JL Smiglak M Drab DM Parker TG Dykes HW Di Salvo R Reich AJ Rogers RD 《Chemical communications (Cambridge, England)》2010,46(47):8965-8967
In this proof of concept study, the ionic liquids, 2-hydroxyethylhydrazinium nitrate and 2-hydroxyethylhydrazinium dinitrate, ignited on contact with preheated Shell 405 (iridium supported on alumina) catalyst and energetically decomposed with no additional ignition source, suggesting a possible route to hydrazine replacements. 相似文献
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Shi Xunqing Wang Zhiping John HL Pang Zhang Xueren Nie Jingxu 《Acta Mechanica Sinica》2002,18(3):274-287
In this study, a new unified creep constitutive relation and a modified energy-based fatigue model have been established respectively
to describe the creep flow and predict the fatigue life of Sn−Pb solders. It is found that the relation successfully elucidates
the creep mechanism related to current constitutive relations. The model can be used to describe the temperature and frequency
dependent low cycle fatigue behavior of the solder. The relation and the model are further employed in part II to develop
the numerical simulation approach for the long-term reliability assessment of the plastic ball grid array (BGA) assembly.
The project supported by the National Natural Science Foundation of China (59705008) 相似文献
9.
Bikiel DE González Solveyra E Di Salvo F Milagre HM Eberlin MN Corrêa RS Ellena J Estrin DA Doctorovich F 《Inorganic chemistry》2011,50(6):2334-2345
A new family of compounds is presented as potential carbon monoxide releasing molecules (CORMs). These compounds, based on tetrachlorocarbonyliridate(III) derivatives, were synthesized and fully characterized by X-ray diffraction, electrospray mass spectrometry, IR, NMR, and density functional theory calculations. The rate of CO release was studied via the myoglobin assay. The results showed that the rate depends on the nature of the sixth ligand, trans to CO, and that a significant modulation on the release rate can be produced by changing the ligand. The reported compounds are soluble in aqueous media, and the rates of CO release are comparable with those for known CORMs, releasing CO at a rate of 0.03-0.58 μM min(-1) in a 10 μM solution of myoglobin and 10 μM of the complexes. 相似文献
10.
Summary It is shown that in the presence of a crossed electric and magnetic field the electronic states of a semiconductor in the
effective-mass approximation are described by a Hamiltonian containing a non-local potential. In order to preserve the gauge
invariance of the two-photon interband transition rate, the interaction Hamiltonian between the electrons and the incident
radiation has to be generalized. For GaAs, the transition rate between two particular levels is evaluated in both length and
velocity gauges demonstrating the correctness of our approach.
Work partially supported by the European Community Programme ESPRIT, Basic research, action n. 6878, EASI. 相似文献