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1.
Europium (Eu+) ions were confined in a Paul trap and detected by non-destructive method. Storage time of Eu+ ions achieved in vacuum was improved by orders of magnitude employing buffer gas cooling. The experimentally detected signal
was fitted to the ion response signal and the total number of ions trapped was estimated. It is found that the peak signal
amplitude as well as the product of FWHM and the peak signal amplitude is proportional to the total number of trapped ions.
The trapped ion secular frequency was swept at different rates and its effect on the absorption line profile was studied both
experimentally and theoretically. 相似文献
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Probing the water coordination of protein-targeted MRI contrast agents by pulsed ENDOR spectroscopy.
Stephan G Zech Wei-Chuan Sun Vincent Jacques Peter Caravan Andrei V Astashkin Arnold M Raitsimring 《Chemphyschem》2005,6(12):2570-2577
A novel methodology based on electron-nuclear double resonance (ENDOR) spectroscopy is used for the direct determination of the water coordination number (q) of gadolinium-based magnetic resonance imaging (MRI) contrast agents. Proton ENDOR spectra can be obtained at approximately physiological concentrations for metal complexes in frozen aqueous solutions either in the presence or absence of protein targets. It is shown that, depending on the structure of the co-ligand, the water hydration number of a complex in aqueous solution can be significantly different to when the complex is noncovalently bound to a protein. From the ENDOR spectra of the exchangeable protons, precise information on the metal-proton distance can be derived as well. These essential parameters directly correlate with the efficacy of MRI contrast agents and should therefore aid the development of novel, highly efficient compounds targeted to various proteins. 相似文献
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Jörg Senn-Bilfinger John R. Ferguson Keith W. Lumbard Karl Zech Peter J. Zimmermann 《Tetrahedron letters》2006,47(19):3321-3323
Glucuronide conjugates of Soraprazan (BY359), a potent novel anti-secretory drug (currently in Phase II clinical trials), were not directly accessible synthetically. This was due to the relative instability of Soraprazan under the harsh Lewis acid conditions employed in popular glucuronidation methodologies and a lack of reactivity under alternative, Koenigs-Knorr, coupling conditions. We have now devised a successful synthesis using the novel N-acetylated Soraprazan to access the required glucuronide metabolites on gram scale. Coupling of this novel aglycone with methyl 1-O-trichloroacetimidoyl-2,3,5-tri-O-isobutyryl-α-d-glucopyran-uronate in the presence of trimethylsilyl trifluoromethanesulfonate (TMSOTf) gave the protected glucuronide intermediates. A one-pot two-step deprotection involving hydrolysis of the ester functionalities and removal of the N-acetyl group with alkaline hydrazine delivered the title compounds in satisfactory yield. 相似文献
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The ground state nuclear moments of186Ir (j π=5(+)) have been determined with NMR on oriented186Ir in Ni as |μ|=3.80 ?0.02 +0.12 μ n andQ=?3.00 (15)b. The quadrupole moment is consistent with an anamolousj π K=5+0 or 5+1 ground state configuration. The explanation of the magnetic moment in terms of pure 5+0 or 5+1 configurations would require a high collectiveg R-factor ofg R≧0.76. On the other hand the magnetic moment can be explained with a “normal”g R and a mixed ground state configuration. 相似文献
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G. Zech F. Dydak F.L. Navarria O.E. Overseth P. Steffen H. Wahl E.G.H. Williams C. Geweniger K. Kleinknecht H. Taureg 《Nuclear Physics B》1977,124(4):413-425
The mean lifetimes of the Λ and Ξ0 hyperons have been measured in a short neutral beam at the CERN Proton Synchrotron. Λ and Ξ0 decays have been identified by measuring their decay products in a magnetic spectrometer and in a lead glass hodoscope. The experimental results, based on 53 000 Λ decays and 6300 Ξ0 decays are From the result for τΞ0 together with existing data on τΞ? we obtain a violation of the rule in non-leptonic Ξ decays. 相似文献
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Zech SG Olejniczak E Hajduk P Mack J McDermott AE 《Journal of the American Chemical Society》2004,126(43):13948-13953
A novel approach for detection of ligand binding to a protein in solid samples is described. Hydrated precipitates of the anti-apoptotic protein Bcl-xL show well-resolved (13)C-(13)C 2D solid-state NMR spectra that allow site-specific assignment of resonances for many residues in uniformly (13)C-enriched samples. Binding of a small peptide or drug-like organic molecule leads to changes in the chemical shift of resonances from multiple residues in the protein that can be monitored to characterize binding. Differential chemical shifts can be used to distinguish between direct protein-ligand contacts and small conformational changes of the protein induced by ligand binding. The agreement with prior solution-state NMR results indicates that the binding pocket in solid and liquid samples is similar for this protein. Advantages of different labeling schemes involving selective (13)C enrichment of methyl groups of Ala, Val, Leu, and Ile (Cdelta1) for characterizing protein-ligand interactions are also discussed. It is demonstrated that high-resolution solid-state NMR spectroscopy on uniformly or extensively (13)C-enriched samples has the potential to screen proteins of moderate size ( approximately 20 kDa) for ligand binding as hydrated solids. The results presented here suggest the possibility of using solid-state NMR to study ligand binding in proteins not amenable to solution NMR. 相似文献