全文获取类型
收费全文 | 1088篇 |
免费 | 46篇 |
国内免费 | 4篇 |
专业分类
化学 | 769篇 |
晶体学 | 7篇 |
力学 | 17篇 |
数学 | 121篇 |
物理学 | 224篇 |
出版年
2023年 | 4篇 |
2022年 | 7篇 |
2021年 | 26篇 |
2020年 | 22篇 |
2019年 | 17篇 |
2018年 | 19篇 |
2017年 | 8篇 |
2016年 | 37篇 |
2015年 | 32篇 |
2014年 | 38篇 |
2013年 | 51篇 |
2012年 | 63篇 |
2011年 | 91篇 |
2010年 | 49篇 |
2009年 | 49篇 |
2008年 | 75篇 |
2007年 | 62篇 |
2006年 | 62篇 |
2005年 | 60篇 |
2004年 | 53篇 |
2003年 | 35篇 |
2002年 | 44篇 |
2001年 | 28篇 |
2000年 | 19篇 |
1999年 | 12篇 |
1998年 | 13篇 |
1997年 | 10篇 |
1996年 | 8篇 |
1995年 | 7篇 |
1994年 | 6篇 |
1993年 | 8篇 |
1992年 | 9篇 |
1991年 | 10篇 |
1990年 | 11篇 |
1989年 | 6篇 |
1988年 | 7篇 |
1987年 | 4篇 |
1986年 | 7篇 |
1985年 | 7篇 |
1984年 | 11篇 |
1983年 | 5篇 |
1982年 | 12篇 |
1981年 | 6篇 |
1980年 | 3篇 |
1979年 | 4篇 |
1978年 | 3篇 |
1975年 | 2篇 |
1970年 | 4篇 |
1963年 | 2篇 |
1916年 | 2篇 |
排序方式: 共有1138条查询结果,搜索用时 125 毫秒
41.
42.
[reaction: see text] The reaction of alpha-alkoxy aldehydes with Et4NAg(CN)2 or Me3SiCN in the presence of MgBr2 x OEt2 in CH2Cl2 at 0 degrees C gives the corresponding syn cyanohydrins in good yield with high diastereoselectivity. Excess MgBr2 x OEt2 (typically 5 equiv) is required for high diastereoselectivity. Et4NAg(CN)2 (but not Me3SiCN) is sufficiently reactive to give cyanohydrins at -78 degrees C, and higher diastereoselectivity is obtained at this temperature. 相似文献
43.
Narcís Homs Jordi Llorca Montserrat Riera Jordi Jolis Jos-Luis G. Fierro Joaquim Sales Pilar Ramírez de la Piscina 《Journal of molecular catalysis. A, Chemical》2003,200(1-2):251-259
Silica-supported trimetallic catalysts containing Pt, Sn and a group 13 metal (PtSnM, M=Ga, In, Tl) were prepared by consecutive impregnation steps from cis-[PtCl2(PPh3)2] and chloride precursors. X-ray diffraction (XRD), transmission electron microscopy (TEM), selected-area electron diffraction (ED) and energy dispersive X-ray analysis (EDX) showed large platelet-like particles of PtSn1−xMx phases. PtSnGa catalyst with a Pt/(Sn+Ga) molar ratio of 1.72 showed a bimodal particle distribution and a Pt phase was identified. Differences in surface structures were also revealed by the performance of catalysts in the dehydrogenation of n-hexane. For PtSnIn and PtSnTl (Pt/(Sn+M) molar ratio of about 1) the dehydrogenation was favoured. In contrast, PtSnGa catalyst yielded hydrogenolysis products. Photoelectron spectra showed the Pt 4f7/2 level at a binding energy of 70.0–71.8 eV in all cases. Moreover, the FT-IR spectra of chemisorbed CO on the PtSnGa showed a slight shift in the ν(CO) toward higher values with respect to the monometallic catalyst, pointing to an electronic effect in accordance with photoelectron spectroscopy. 相似文献
44.
Zully A. Benzo Manuelita Velosa Claudio Ceccarelli Miguel Guardia Amparo Salvador 《Fresenius' Journal of Analytical Chemistry》1991,339(4):235-239
Summary The literature on the application of the slurry technique to biological materials is reviewed. It is obvious from the various applications that the most frequently employed atomization method for slurry analysis in biological materials is electrothermal atomization using either graphite tube or platform atomizers. The slurry technique is particularly useful when certified reference materials are not available and when the standard addition method is to be avoided. The literature survey revealed that this technique compares favourably with other methods for the determination of trace metals in biological materials. 相似文献
45.
46.
A fast procedure has been developed for the direct determination of paint solvents. The method is based on the injection of small volumes of untreated solvent mixtures into a heated Pyrex glass reactor in which the sample is volatilized and introduced by means of a flow of nitrogen into an IR multiple pass gas cell and the spectrum in the mid-IR region is registered as a function of time. Data found for samples are interpolated in calibration graphs obtained by injecting different volumes of pure compounds which constitute the solvent mixture. A methylisobutylketone (MIBK) toluene mixture was used as test system to develop the proposed procedure. The method provides a limit of detection of the order of 1–4 μg, a relative standard deviation of the order of 0.4 to 2% for five independent measurements, and recovery percentage values from 99.8 till 103.6 %. A commercial sample of polyurethane paint solvent has been analysed by the developed procedure. 相似文献
47.
Adrian Hernandez Santiago Salvador Rosas Castilla Albino Morales Rodriguez Elena Aleskerova Anastasia Lantushenko Viktor Kostjukov 《Molecular physics》2013,111(15):1941-1947
An approximately linear correlation has been found between the enthalpy of complexation and the area of overlap of the chromophores using published structural and thermodynamical data on the self- and hetero-association of aromatic molecules measured under similar solution conditions. This finding is consistent with the assumption that short-range van-der-Waals forces dominate over other contributions to the enthalpy of stacking of aromatic molecules. It provides a ‘model-independent’ approach for a priori estimation of the enthalpy of aromatic–aromatic stacking interactions from knowledge of the structural properties or vice versa. 相似文献
48.
Exploring the Effect of Ligand Structural Isomerism in Langmuir–Blodgett Films of Chiral Luminescent EuIII Self‐Assemblies 下载免费PDF全文
Agostino Galanti Dr. Oxana Kotova Dr. Salvador Blasco Chloe J. Johnson Dr. Robert D. Peacock Shaun Mills Prof. John J. Boland Prof. Martin Albrecht Prof. Thorfinnur Gunnlaugsson 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(28):9709-9723
Here we have investigated the influence of the antenna group position on both the formation of chiral amphiphilic EuIII‐based self‐assemblies in CH3CN solution and, on the ability to form monolayers on the surface of quartz substrates using the Langmuir–Blodgett technique, by changing from the 1‐naphthyl ( 2(R) , 2(S) ) to the 2‐naphthyl ( 1(R) , 1(S) ) position. The evaluation of binding constants of the self‐ assemblies in CH3CN solution was achieved using conventional techniques such as UV/Visible and luminescence spectroscopies along with more specific circular dichroism (CD) spectroscopy. The binding constants obtained for EuL , EuL2 and EuL3 species in the case of 2‐naphthyl derivatives were comparable to those obtained for 1‐naphthyl derivatives. The analysis of the changes in the CD spectra of 1(R) and 1(S) upon addition of EuIII not only allowed us to evaluate the values of the binding constants but the resulting recalculated spectra may also be used as fingerprints for assignment of the chiral self‐assembly species formed in solution. The obtained monolayers were predominantly formed from EuL3 (≈85 %) with the minor species present in ≈15 % EuL2 . 相似文献
49.
José Roberto dos Santos Politi Paulo Roberto Rodrigues de Matos Maria José Araújo Sales 《Journal of Thermal Analysis and Calorimetry》2013,111(2):1437-1442
Demand for lubricating oils is increasing in the growing Brazilian economy. The use of vegetable bases in exchange of minerals can bring socio-economic and environmental benefits for Brazil. The purpose of this study is to compare the thermal and oxidative stability of vegetable oils related to the bases commonly used as lubricants. In this study, thermogravimetric analysis of castor oil, cotton oil, macauba’s almond oil, passion oil, paraffinic mineral oil, naphthenic oil (NH-140) and synthetic oil (Etro) was performed in inert and oxidative atmosphere to study the thermal and oxidative degradation of the vegetable oils related to the most common lubricants’ oils base. These oils’ oxidation stability were determined by standard procedures (ISO 6886). The use of mineral oil’s additives in these vegetable oils was tested to verify the viability of these additives to improve the oxidative stability of the vegetable oils. The castor oil and the cotton oil presented results of thermal analysis similar to the mineral and synthetic bases values. The castor oil was the only vegetable oil that showed a great oxidative stability. All other vegetable oils had their oxidative stability significantly increased by the additives. 相似文献