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41.
通过采用真空紫外(VUV)激光速度-地图成像-TPE(真空紫外VMI-TPE)方法获得了高分辨率初始光电子(TPE)氯苯(C6H5Cl(X1A1))的光谱,炔丙基自由基(C3H3(X2B1))和烯丙基(C3H5(X2A1)). 观察到的真空紫外VMI-TPE方法的光电子能量分辨率在1~2 cm-1,可以和在真空紫外激光脉冲场电离光电子(VUV-PFI-PE)的测量媲美. 类似真空紫外PFI-PE测量,真空紫外VMI-光电子(真空紫外VMI-PE)和真空紫外VMI-TPE测量能量分辨率依赖于直流电场在光电离区加速电子. C6H5Cl和C3H3的电离初始值的降低为F的函数表示Stark偏移校正为VUV-VMI-TPE测量由-3.1√F管辖,这是半经典预测值-6.1√F的一半. 我们还测量C6H5Cl和C3H5的真空紫外光能量的真空紫外VMI-PE谱接近其电离初始值. 在VUV-VMI-PE测量中观察到的C3H5+阳离子振动谱和振动级数,nv7+(n=0~3). 真空紫外VMI-TPE可以实现更高的实验灵敏度和类似真空紫外PFI-PE测量的能量分辨率,使真空紫外VMI-TPE法成为高分辨率真空紫外PFI-PE测量一个很好的替代.  相似文献   
42.
In this article the utility of phosphoramidite ligands in enantioselective Au(I) catalysis was explored in the development of highly diastereo- and enantioselective Au(I)-catalyzed cycloadditions of allenenes. A Au(I)-catalyzed synthesis of 3,4-disubstituted pyrrolidines and γ-lactams is described. This reaction proceeds through the enantioselective Au(I)-catalyzed cyclization of allenenes to form a carbocationic intermediate that is trapped by an exogenous nucleophile, resulting in the highly diastereoselective construction of three contiguous stereogenic centers. A computational study (DFT) was also performed to gain some insight into the underlying mechanisms of these cycloadditions. The utility of this new methodology was demonstrated through the formal synthesis of (-)-isocynometrine.  相似文献   
43.
A novel hydrogen migration from the phenyl ring to the pyridine ring of an yttrium pyridyl complex supported by a 1,1'-ferrocene diamide ligand is reported. Density functional theory calculations were instrumental in probing the mechanism for this transformation.  相似文献   
44.
The membrane extraction of Y, Ce, Eu, Tm and their binary mixtures Ce–Y, Ce–Eu, Ce–Tm with supported liquid membranes containing TBP and HDEHP as carriers in decanedodecane hydrocarbon solvent, has been studied. Upon extraction with TBP aqueous nitrate solutions of rare earth elements (REE) were used as feed phase. In some cases they also contained EDTA or DCTA. In most cases, the receiving phase was an aqueous solution of EDTA. Extraction with HDEHP was performed from nitrate and chloride solutions and the receiving phase was the corresponding dilute acid. Pertraction of an element through a membrane was studied as a function of time and of initial composition of phases. The results are presented in the following forms: flux of metal through membrane, coefficients of permeability, separation factors and effective diffusion coefficients.  相似文献   
45.
46.
[reaction: see text] A chiral periodic mesoporous organosilica (ChiMO) was prepared, in which a 1,2-bis-(ureido)cyclohexyl linker (38 wt %) is introduced into the walls of the hybrid organic-inorganic material. This silica was used as a host for 11-formyl-12-methyldibenzobarrelene (2), and the stereoselectivity of the di-pi-methane rearrangement of 2 within this host-guest complex was studied. At low conversions, the only product was the corresponding dibenzosemibullvalene. An enantiomeric excess of 24% at 11% conversion was obtained using the ChiMO as host. These values compare well with those achieved using a system based on conventional faujasites (LiY and NaY) as hosts incorporating a chiral auxiliary. We tested S-phenylglycine, S-proline, S-camphanic acid, and S-mandelic acid as chiral auxiliaries. In contrast to the behavior of the ChiMO material, adsorption of dibenzobarrelene in purely siliceous mesoporous MCM-41 silica (3.2 nm pore size) containing ephedrine failed, a failure that can be explained as arising from the large internal silanol population and high hydrophilicity of the siliceous MCM-41 sample.  相似文献   
47.
48.
Starting from colloidal TiO2 nanoparticles in combination with tetraethyl orthosilicate using neutral Pluronic or cationic cetyltrimethylammonium as templates, a series of structured mesoporous silicas has been obtained. The structure of the mesoporous titania was confirmed by isothermal gas adsorption, transmission electron microscopy, and X-ray diffraction. The pore diameter ranged between 3.8 and 10.9 nm, and the BET surface area varied from 99 to 584 m2 g(-1). The photocatalytic activity of these samples for the degradation of phenol in aqueous solution has been compared with that of standard P-25 TiO2. Even though the activity of these new mesostructured materials is lower that those found for P-25 TiO2, the turnover frequency of the photocatalytic activity (moles of phenol degraded per Ti atom present at initial reaction time) is much higher for the mesoporous titania, particularly with low titanium contents for those materials (mpTiO2-5 and TiO2SBA15-5).  相似文献   
49.
We report results of a search for particles with anomalously high ionization in events with a high transverse energy jet and large missing transverse energy in 2.4 fb?1 of integrated luminosity collected by the D0 experiment at the Fermilab Tevatron pp collider. Production of such particles (quirks) is expected in scenarios with extra QCD-like SU(N) sectors, and this study is the first dedicated search for such signatures. We find no evidence of a signal and set a lower mass limit of 107, 119, and 133 GeV for the mass of a charged quirk with strong dynamics scale Λ in the range from 10 keV to 1 MeV and N=2, 3, and 5, respectively.  相似文献   
50.
We report a search for diphoton events with large missing transverse energy produced in pp collisions at √s=1.96 TeV. The data were collected with the D0 detector at the Fermilab Tevatron Collider and correspond to 6.3 fb(-1) of integrated luminosity. The observed missing transverse energy distribution is well described by the standard model prediction, and 95% C.L. limits are derived on two realizations of theories beyond the standard model. In a gauge-mediated supersymmetry breaking scenario, the breaking scale Λ is excluded for Λ<124 TeV. In a universal extra dimension model including gravitational decays, the compactification radius R(c) is excluded for R(c)(-1)<477 GeV.  相似文献   
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