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201.
We introduce a full-field fluorescence imaging technique with axial confinement of about 100 nm at the sample/substrate interface. Contrary to standard surface imaging techniques, this confinement is obtained through emission filtering. This technique is based on supercritical emission selectivity. It can be implemented on any epifluorescence microscope with a commercial high numerical aperture objective and offers a real-time surface imaging capability. This technique is of particular interest for live cell membrane and adhesion studies. Using human embryonic kidney cells, we show that one can observe simultaneously the surface and in-depth cell phenomena. 相似文献
202.
Augusto Rivera Diego Quiroga Jaime Ríos‐Motta Karla Fejfarov Michal Duek 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(12):o505-o508
The title compound, C7H12N4O2, was obtained by nitrosation of the aminal cage (2R,7R,11S,16S)‐1,8,10,17‐tetraazapentacyclo[8.8.1.18,17.02,7.011,16]icosane. The crystal structure is a racemic mixture of RR and SS enantiomers. The asymmetric unit contains two crystallographically independent half‐molecules, one having two partially occupied conformers with refined occupancy factors of 0.747 (3) and 0.253 (3). The molecules sit across twofold axes. The unique molecules each form chains parallel to [001], with molecules connected by intermolecular C—H...O hydrogen bonds. The bonding between adjacent chains is weak. The analysis of eight different crystals confirmed the presence of disordered and nondisordered molecules in the same structure as a regular feature. 相似文献
203.
Jan Fbry Michal Duek Karla Fejfarov Radmila Krupkov Pemysl Vank Ivan Nmec 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):m426-m430
A phase transition was found to occur at ∼153 K in the title compound, (C8H20N)2[PdCl6]. The structures of the two phases are reported at 292 and 130 K. The low‐temperature phase is twinned. The phase transition is accompanied by a minor displacement of the ions. There are C—H⋯Cl interactions as short as ∼2.80 Å, indicating the existence of hydrogen bonds, and this was confirmed by vibrational spectroscopy. The [Pd2Cl6]2− anion occupies sites of mmm and 2/m symmetry in the room‐temperature and low‐temperature phases, respectively. 相似文献
204.
Sourav Chakraborty Eric Schreiber Karla R. Sanchez-Lievanos Mehrin Tariq William W. Brennessel Kathryn E. Knowles Ellen M. Matson 《Chemical science》2021,12(38):12744
We report the synthesis and characterisation of a series of siloxide-functionalised polyoxovanadate–alkoxide (POV–alkoxide) clusters, [V6O6(OSiMe3)(OMe)12]n (n = 1−, 2−), that serve as molecular models for proton and hydrogen-atom uptake in vanadium dioxide, respectively. Installation of a siloxide moiety on the surface of the Lindqvist core was accomplished via addition of trimethylsilyl trifluoromethylsulfonate to the fully-oxygenated cluster [V6O7(OMe)12]2−. Characterisation of [V6O6(OSiMe3)(OMe)12]1− by X-ray photoelectron spectroscopy reveals that the incorporation of the siloxide group does not result in charge separation within the hexavanadate assembly, an observation that contrasts directly with the behavior of clusters bearing substitutional dopants. The reduced assembly, [V6O6(OSiMe3)(OMe)12]2−, provides an isoelectronic model for H-doped VO2, with a vanadium(iii) ion embedded within the cluster core. Notably, structural analysis of [V6O6(OSiMe3)(OMe)12]2− reveals bond perturbations at the siloxide-functionalised vanadium centre that resemble those invoked upon H-atom uptake in VO2 through ab initio calculations. Our results offer atomically precise insight into the local structural and electronic consequences of the installation of hydrogen-atom-like dopants in VO2, and challenge current perspectives of the operative mechanism of electron–proton co-doping in these materials.We report the synthesis and characterisation of a series of siloxide-functionalised polyoxovanadate–alkoxide clusters, [V6O6(OSiMe3)(OMe)12]n (n = 1−, 2−), that serve as molecular models for proton and hydrogen-atom uptake in vanadium dioxide. 相似文献
205.
206.
Sanhueza Luis Garrido Karla Celis Freddy García Macarena Cáceres Cesar Moczko Ewa Díaz Ramiro J. Aguirre María García Camilo 《Journal of Solid State Electrochemistry》2023,27(6):1511-1521
Journal of Solid State Electrochemistry - Screen-printed electrodes (SPEs) have the advantage of being considered electrochemical cells that can be implemented in portable sensor applications. With... 相似文献