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111.
Dr. Hong Yang Dr. Yongcheng Wang Xiang Li Yu Teng Dr. Yulin Tian 《ChemistryOpen》2021,10(10):1013-1019
A smart fluorescence “turn-on” probe which contained a dansyl amide fluorophore and an N-oxide group was designed based on the bioorthogonal decaging reaction between N-oxide and the boron reagent. The reaction proceeds in a rapid kinetics (k2=57.1±2.5 m −1 s−1), and the resulting reduction product showcases prominent fluorescence enhancement (up to 72-fold). Time dependent density functional theoretical (TD-DFT) calculation revealed that the process of photoinduced electron transfer (PET) from the N-oxide moiety to the dansyl amide fluorophore accounts for the quenching mechanism of N-oxide. This probe also showed high selectivity over various nucleophilic amino acids and good biocompatibility in physiological conditions. The successful application of the probe in HaloTag protein labeling and HepG2 live-cell imaging proves it a valuable tool for visualization of biomolecules. 相似文献
112.
We prove that any bounded Fatou component of a polynomial of degree at least two, which is not(eventually) a Siegel disk, is a Jordan domain. 相似文献
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114.
Electroreduction of Dy(III) assisted by Zn and its co-deposition with Zn(II) in LiCl–KCl molten salt
Wenlong Li Wei Han Mei Li Yongcheng Zhang Yingchun Zhang Mengti Yue Yang Sun 《应用有机金属化学》2020,34(10):e5817
To recover dysprosium (Dy) from LiCl–KCl molten salt, the electrochemical mechanism of Dy(III) on liquid Zn electrode and co-deposition of Dy(III) and Zn(II) on W electrode were studied using electrochemical methods. Cyclic voltammetry results demonstrated that the redox process of Dy on liquid Zn electrode is reversible and controlled by diffusion. Reverse chronopotentiograms showed that the transition time ratio of reduction and oxidation is ~3:1, revealing the redox of Dy on liquid Zn electrode is a kind of soluble–soluble system: Dy(III) + 3e− = (Dy–Zn)solution. The half-wave potential of Dy(III) was almost constant with the increase in scanning rate. The electrochemical separation of metallic Dy from the molten salt was performed using constant potential electrolysis, and the product characterized using X-ray diffraction and scanning electron microscopy–energy-dispersive X-ray spectroscopy was the thermodynamic unstable compound DyZn5. Also, the co-deposition mechanism of Dy(III) and Zn(II) was explored, indicating that Dy(III) could deposit on pre-deposited Zn and form Dy–Zn compounds: Zn(II) + 2e− = Zn and xDy(III) + yZn + 3xe− = DyxZny. Moreover, the effect of Dy(III) concentration on the formation of Dy–Zn compounds was investigated. The redox peak currents corresponding to different Dy–Zn compounds changed with the increase in Dy(III) concentration. The co-deposition of Dy(III) and Zn(II) was performed using constant current electrolysis at diverse Dy(III) concentrations. The different Dy–Zn compounds were produced by controlling Dy(III) concentration. 相似文献
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116.
对甲苯磺酰胺基乙酰腙类化合物的生物活性及其量子化学计算 总被引:3,自引:0,他引:3
以对甲苯磺酰氯为原料, 通过与氨基乙酸反应得到中间体对甲苯磺酰氨基乙酸, 再经酯化、肼解得到对甲苯磺酰氨基乙酰肼, 然后与相应的醛缩合得一系列对甲苯磺酰胺基乙酰腙类化合物. 其结构经元素分析, IR, 1H NMR和13C NMR确证. 采用量子化学方法, 在DFT-B3LYP/6-31G*水平上计算了标题化合物4a~4g的反应热、电荷分布和前线轨道能级. 初步生物活性试验结果表明该系列部分化合物在不同浓度下对植物的生长调节表现出一定的规律性. 相似文献
117.
We study the quasisymmetric geometry of the Julia sets of McMullen maps fλ(z) = zm + λ/z?, where λ ∈ ? {0} and ? and m are positive integers satisfying 1/?+1/m < 1. If the free critical points of fλ are escaped to the infinity, we prove that the Julia set Jλ of fλ is quasisymmetrically equivalent to either a standard Cantor set, a standard Cantor set of circles or a round Sierpiński carpet (which is also standard in some sense). If the free critical points are not escaped, we give a suffcient condition on λ such that Jλ is a Sierpiński carpet and prove that most of them are quasisymmetrically equivalent to some round carpets. In particular, there exist infinitely renormalizable rational maps whose Julia sets are quasisymmetrically equivalent to the round carpets. 相似文献
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119.
Zening Liu Yongcheng Liu Mujin Cai Piaopiao Xu Zonghua Ma Hong Yuan 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2017,91(3):500-510
Magnetically separable Fe3O4/AgCl photocatalysts were prepared by a one-pot sequential method. A series of techniques proved the hybrid structure of Fe3O4/AgCl composites. Fe3O4/AgCl composites had a much higher photocatalytic activity toward Rhodamine B (RhB) degradation than pure AgCl under the simulated solar light irradiation. The existence of metal Ag resulted in high photocatalytic activity of Fe3O4/AgCl, which was related with the amount of metallic Ag. The scavenging experiments showed that the degradation reaction most probably was initiated by the photoinduced single-electron transfer, and the generation of superoxide anion (O 2 -· ) played a significant role. The composite photocatalysts could be recycled by applying an external magnetic field, and the reused composites maintained their original photocatalytic activity. Fe3O4/AgCl composites were highly efficient, magnetically separable, and recoverable. This proves their potential applications in the photodegradation of organic pollutants. 相似文献
120.
基于密度泛函理论第一性原理研究了以单空位缺陷(SV)石墨烯为载体的Pt,Fe及PtFe二元金属催化剂的抗CO中毒能力.结果表明,对于单金属原子Pt和Fe,Fe更易吸附在SV石墨烯上;而对于PtFe二元金属催化剂,SV石墨烯对其固定能力明显好于Pt-SV,即Pt催化剂中掺杂Fe大大增加了SV石墨烯对金属催化剂的稳定性.Pt,Fe及PtFe二元金属催化剂抗CO中毒能力的研究结果表明,PtFe-6结构的抗CO中毒能力明显强于Pt-SV,接近于Fe-SV的抗CO中毒能力,在所有二元金属催化剂中PtFe-6的稳定性最好,明显优于Pt在SV石墨烯上的稳定性.通过在Pt中加入非贵金属Fe既可提高DMFC中阳极Pt催化剂的抗CO中毒能力,又可提高其催化活性. 相似文献