全文获取类型
收费全文 | 659篇 |
免费 | 33篇 |
国内免费 | 15篇 |
专业分类
化学 | 474篇 |
晶体学 | 2篇 |
力学 | 43篇 |
数学 | 76篇 |
物理学 | 112篇 |
出版年
2023年 | 2篇 |
2022年 | 8篇 |
2021年 | 12篇 |
2020年 | 27篇 |
2019年 | 26篇 |
2018年 | 35篇 |
2017年 | 34篇 |
2016年 | 61篇 |
2015年 | 38篇 |
2014年 | 41篇 |
2013年 | 100篇 |
2012年 | 52篇 |
2011年 | 73篇 |
2010年 | 28篇 |
2009年 | 35篇 |
2008年 | 26篇 |
2007年 | 24篇 |
2006年 | 11篇 |
2005年 | 15篇 |
2004年 | 11篇 |
2003年 | 18篇 |
2002年 | 11篇 |
2001年 | 4篇 |
2000年 | 2篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1987年 | 2篇 |
1984年 | 1篇 |
1976年 | 2篇 |
排序方式: 共有707条查询结果,搜索用时 15 毫秒
21.
Let G be a 2k-edge-connected graph with and let for every . A spanning subgraph F of G is called an L-factor, if for every . In this article, we show that if for every , then G has a k-edge-connected L-factor. We also show that if and for every , then G has a k-edge-connected L-factor. 相似文献
22.
A series of dinuclear cycloplatinated(II) complexes with general closed formula of [Pt2Me2(C^N)2(μ‐P^P)] (C^N = 2‐vinylpyridine (Vpy), 2,2′‐bipyridine N‐oxide (O‐bpy), 2‐(2,4‐difluorophenyl)pyridine (dfppy); P^P = 1,1‐bis(diphenylphosphino)methane (dppm), N,N‐bis(diphenylphosphino)amine (dppa)) are reported. The complexes were characterized by means of NMR spectroscopy. Due to the presence of dppm and dppa with short backbones as bridging ligands, two platinum centres are located in front of each other in these complexes so a Pt…Pt interaction is established. Because of this Pt…Pt interaction, the complexes have bright orange colour under ambient light and are able to strongly emit red light under UV light exposure. These strong red emissions originate from a 3MMLCT (metal–metal‐to‐ligand charge transfer) electronic transition. In most of these complexes, the emissions have unstructured bell‐shaped bands, confirming the presence of large amount of 3MMLCT character in the emissive state. Only the complexes bearing dfppy and dppa ligands reveal dual luminescence: a high‐energy structured emission originating from 3ILCT/3MLCT (intra‐ligand charge transfer/metal‐to‐ligand charge transfer) and an unstructured low‐energy band associated with 3MMLCT. In order to describe the nature of the electronic transitions, density functional theory calculations were performed for all the complexes. 相似文献
23.
Reaction pathways of ethylene and carbon monoxide on the singlet and triplet potential energy surfaces (PESs) have been calculated at B3LYP/6-311++G (3df, 3dp), G3B3 and CCSD(T)//B3LYP levels. Reaction mechanisms have been investigated by analysis of various structures. Suggested reaction mechanisms reveal that 3P3(CH2CHCHO) and 3P4(CH3CCHO) are thermodynamically stable adducts with the negative value in Gibbs free energies on the triplet PES. In addition, results show that one intersystem crossing exists between triplet and singlet PESs, which are obtained by scanning of the C–C bond length in 1IN3 and 3IN7 species. 相似文献
24.
25.
26.
27.
28.
29.
M. Montazerozohori 《Journal of Thermal Analysis and Calorimetry》2013,111(1):121-128
Some new coordination compounds of cadmium(II) and mercury(II) with N,N-bis[(E)-3-(phenylprop)-2-enylidene]propanediamine (L) as a new bidentate Schiff base ligand with general formula MLX2 (X = Cl?, Br?, I?, SCN?, and N3 ?) have been prepared. They were characterized by elemental analysis, FT-infrared (FT-IR) and Ultraviolet–Visible spectra, 1H- and 13C-NMR spectra. The reasonable shifts of FT-IR and NMR spectral signals of the complexes with respect to the free ligand confirm well coordination of ligand and anions(X-) in inner sphere coordination mode. The thermal behavior of the complexes from room temperature to 800 °C shows weight loss by decomposition of the anions and ligand segments in the subsequent steps. The results showed that cadmium complexes have no water molecules (neither as lattice nor as coordinated water) and are decomposed in two temperature steps except about cadmium thiocyanate complex that is decomposed in three steps. Final residual contents of cadmium complexes are suggested to be cadmium oxide or sulfide. Mercury complexes were decomposed in three to four temperature steps. Mercury bromide and azide complexes leave out a little amount of mercury oxide in final, while mercury chloride, iodide, and thiocyanate complexes were found to be completely decomposed without any residual matter. 相似文献
30.
Optimization of synthesis procedure and structure characterization of manganese tungstate nanoplates
Mehdi Rahimi-Nasrabadi S. Mahdi Pourmortazavi Morteza Khalilian-Shalamzari S. Somayyeh Hajimirsadeghi M. Mahdi Zahedi 《Central European Journal of Chemistry》2013,11(8):1393-1401
A simple and fast chemical method was used for synthesis of manganese tungstate nanoplates in flower-like clusters; while Taguchi robust design was employed as statistical method for optimization of the experimental parameters for the procedure. Ultrafine manganese tungstate plates in flower-like clusters were synthesized via a direct precipitation method involving addition of manganese ion solution to the aqueous tungstate reagent. Effects of various reaction conditions such as manganese and tungstate concentrations, flow rate of reagent addition and reactor temperature on the thickness of the synthesized manganese tungstate plates were investigated experimentally. Analysis of variance (ANOVA) showed that manganese tungstate nanoplates could be effectively synthesized by tuning significant parameters of precipitation procedure. Meanwhile, optimum conditions for synthesis of MnWO4 nanoplates via this simple, fast, and cost effective method were proposed. The structure and composition of the prepared nanoplates under optimum conditions were characterized by EDX, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), FT-IR spectroscopy, and photoluminescence techniques. 相似文献