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21.
Rajan Adhikari Dr. Jan Brox Stephen Massicot Dr. Michael Ruppel Prof. Dr. Norbert Jux Dr. Hubertus Marbach Prof. Dr. Hans-Peter Steinrück 《Chemphyschem》2023,24(17):e202300539
The front cover artwork is provided by the groups of Prof. Dr. Hans-Peter Steinrück and Prof. Dr. Norbert Jux at the Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg. The image shows a mixture of six 2H-tetrakis-(3, 5-di-tert-butyl-phenyl)(x)benzoporphyrins (2H-diTTBP(x)BPs, x = 0, 1, 2-cis, 2-trans, 3, or 4) molecules forming a porous square structure on Ag(111) as observed in scanning tunneling microscopy (STM) at room temperature. Read the full text of the Research Article at 10.1002/cphc.202300355 . 相似文献
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We have studied the structural behavior of lead monoxide (PbO) as a function of pressure via angular dispersive X-ray diffraction employing two different pressure transmitting media that were quasi-hydrostatic (N2) and non-hydrostatic (MgO), respectively. Besides litharge (-PbO) and massicot (β-PbO), which are both stable at ambient pressure, there is an orthorhombic γ-PbO phase which appears upon application of pressure to -PbO. We have found that the orthorhombic γ-PbO phase is favored by shear stress under non-hydrostatic conditions. -PbO shows strong anisotropy in compressibility. The a-axis is rather incompressible with a linear stiffness coefficient of Ka0=540(30) GPa whereas the c-axis stiffness is Kc0=25(1) GPa. The bulk modulus of -PbO is K0=23.1(3) GPa and its derivative . 相似文献
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Martin Giera Jon S. B. de Vlieger Henk Lingeman Hubertus Irth Wilfried M. A. Niessen 《Rapid communications in mass spectrometry : RCM》2010,24(10):1439-1446
Structural elucidation of six regioisomers of mono‐N‐octyl derivatized neomycin is achieved using MSn (up to n = 4) on an ion trap time‐of‐flight (IT‐TOF) instrument equipped with electrospray ionization. The mixture of six derivatized neomycin analogues was generated by reductive amination in a shotgun synthetic approach. In parallel to the liquid chromatography/mass spectrometry (LC/MS) detection, the antibacterial activity of the neomycin regioisomers was tested by post‐column addition of buffer and bacterial inocula, subsequent microfractionation of the resulting mixture, incubation, and finally a chemiluminescence‐based bioactivity measurement based on the production of bacterial ATP. The MS‐based high‐resolution screening approach described can be applied in medicinal chemistry to help in designing and producing new antibiotic substances, which is particularly challenging due to the high functionality of most antibiotic substances, therefore requiring advanced (hyphenated) separation and detection techniques for compound mixtures. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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Hubert G. Theuns Richard H. A. M. Janssen Hubertus W. A. Biessels Cornelis A. Salemink 《Magnetic resonance in chemistry : MRC》1984,22(12):793-794
13C NMR chemical shifts are assigned for some quaternary morphinan derivatives, including the ‘minor isomer’ of the thebaine N-oxides. In quaternary morphinan alkaloids having an 8.14-double bond, electric field effects cause unusual 13C NMR shifts. 相似文献
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Jonker N Kool J Krabbe JG Retra K Lingeman H Irth H 《Journal of chromatography. A》2008,1205(1-2):71-77
A novel methodology is shown enabling the screening of mixtures of compounds for their affinity to a receptor protein. The system presented, dynamic protein-affinity chromatography solid-phase extraction (DPAC-SPE), overcomes the limitations of the existing methods by performing an incubation of the His-tagged protein with a mixture of possible ligands, which are still in their native conditions. This is followed by a fully automated affinity trapping step, coupled on-line to an LC-MS system in order to detect and identify the bound ligands. The system has been optimized using a commercially available on-line SPE system, using the estrogen receptor alpha (ERalpha) as model protein. A representative range of ligands with sub-nanomolar to millimolar affinities has been identified successfully from a mixture. The weakest binder that can be identified is norethindrone (approximately K(d)=0.1-1mM). The same setup also provides the possibilities to measure EC50 curves of both weak and strong binders. 相似文献