全文获取类型
收费全文 | 140篇 |
免费 | 7篇 |
国内免费 | 2篇 |
专业分类
化学 | 89篇 |
晶体学 | 1篇 |
力学 | 7篇 |
数学 | 24篇 |
物理学 | 28篇 |
出版年
2023年 | 3篇 |
2022年 | 1篇 |
2021年 | 3篇 |
2020年 | 1篇 |
2019年 | 3篇 |
2018年 | 3篇 |
2017年 | 1篇 |
2016年 | 2篇 |
2015年 | 6篇 |
2014年 | 5篇 |
2013年 | 4篇 |
2012年 | 14篇 |
2011年 | 14篇 |
2010年 | 5篇 |
2009年 | 4篇 |
2008年 | 10篇 |
2007年 | 12篇 |
2006年 | 8篇 |
2005年 | 11篇 |
2004年 | 5篇 |
2003年 | 3篇 |
2002年 | 5篇 |
2001年 | 3篇 |
2000年 | 2篇 |
1998年 | 1篇 |
1997年 | 1篇 |
1996年 | 3篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1993年 | 3篇 |
1991年 | 1篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1984年 | 1篇 |
1983年 | 2篇 |
1980年 | 1篇 |
1977年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有149条查询结果,搜索用时 31 毫秒
1.
2.
Capillary zone electrophoretic separation and determination of imidazolic antifungal drugs 总被引:1,自引:0,他引:1
Capillary zone electrophoresis (CZE) was adapted to the simultaneous determination of a mixture of three imidazolic antifungal drugs. Separation was achieved by using a fused-silica capillary column with an acetic acid-Tris buffer at pH 5.18 and UV detection at 196 nm. Several electrophoretic parameters were investigated: pH and buffer concentration, applied voltage, temperature and injection conditions. The optimized CZE method was applied to the individual determination of ketoconazole, clotrimazole and econazole in pharmaceutical forms, after a previous single extraction step in methanol, with recoveries of 98.00, 99.96 and 99.58% respectively. The antifungal drugs can be determined at a concentration level lower than 1.0 x 10(-7) M. 相似文献
3.
4.
The stereospecific synthesis of the monoterpene alkaloids (?)-α-skytanthine ((?)- 2 ), (?)-N -demethyle-δ-sky-tanthine((?)- 7 ), and (+)-epidihydrotecomanine (+)- 4 was achieved from a common intermediate 22 , which in turn was obtained from (1R,4S,1′S)-2-(1′-phenylethyl)-2-azabicyclo[2.2.1]hept-5-ene (10) ,via a ketene aza-Claisen rearrangement. The piperidine derivative (+)- 31 , formally the aza-analogue of (+)-isoiridomyrmecin, was also obtained from the same intermediate 22 . 相似文献
5.
The conventional four-step sequential extraction method and the EDTA and acetic acid single extraction procedures were applied to sewage sludge and sediment samples. The results obtained with these samples for Cu, Cr, Ni, Pb and Zn using the Tessier method were compared with those supplied by the two single extraction procedures employed. In addition, the Tessier method was also applied to a reference material, CRM 483, and these results were also compared with the certified EDTA and acetic acid values for this sample. As a result, good agreement was found between the metal contents released in the first three fractions of the Tessier method and those leached by the simpler single extraction procedures for the most of the elements studied. Subsequently, the conventional EDTA and acetic acid extraction methods were accelerated by means of microwave energy, in order to reduce the operating time. The extraction efficiency of the first three fractions of the Tessier method was compared with that obtained using the optimised microwave single extraction procedures and only in sewage sludge and CRM 483 samples were satisfactory results found for all the elements studied, except Cr and Pb. This means that the microwave single extraction procedures optimised in this work could be employed as screening methods to evaluate rapidly the easiest mobilizable heavy metals in these samples, although more samples should be analysed to determine their general applicability. The application of the accelerated single extraction procedures to a reference material, CRM 483, provided satisfactory results for all the elements studied, except for Cr in both methods and for Pb in the acetic acid extracts. 相似文献
6.
Cid MB Alfonso F Martín-Lomas M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(3):928-938
The stereochemical outcome of glycosylations with 2-azido-2-deoxy-D-gluco- and D-galactopyranosyl trichloroacetimidates as glycosyl donors has been investigated by using a series of chiro-inositol derivatives as glycosyl acceptors. The influence of the absolute configuration, the conformation and the conformational flexibility of the glycosyl acceptor has been studied by using different glycosyl donors under similar pre-established experimental conditions. Although the structure of the acceptor may play a role in governing the stereochemistry of these glycosylations, the results show that, in general terms, the relative influence of these factors is difficult to evaluate. For a given set of experimental conditions, the stereochemical course of these glycosylations depends on structural features of both glycosyl donor and glycosyl acceptor. It is a balance of these factors, where the structure of the glycosyl donor always plays a major role, which determines the stereochemistry of the coupling reaction. Therefore, the examples reported in the literature in which the structure of the glycosyl acceptor appears to be crucial in determining the stereochemistry of the reaction constitute particularly favorable cases which do not presently allow any further generalization. 相似文献
7.
Jessica Cid Dr. Jorge J. Carbó Dr. Elena Fernández 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(40):12794-12802
Most trivalent boron reagents are electrophiles owing to the vacancy for two electrons to fill the outer orbital of boron; however, interestingly, trivalent boron compounds can change their electrophilic character to a nucleophilic character by only changing the nature of the substituents on the boron atoms. With the help of computational tools, we have analyzed the structural‐ and electronic properties of boryl fragments that were either bonded to main‐group metals or coordinated to transition‐metals/rare‐earth‐metals and we have designed a map that might help to identify certain trends. This trend map will be useful for selecting an appropriate trivalent boron compound, depending on the sought reactivity. 相似文献
8.
Adrián Serrano Mora Sean T. McBeath Clément A. Cid Michael R. Hoffmann Nigel J.D. Graham 《Current Opinion in Electrochemistry》2022
While diamond electrodes have been commonly used to generate ?OH to treat a variety of persistent water and wastewater micropollutants, mass transfer limitations and the non-selective, short-lived nature of the ?OH restrict the degradation to the solution at, or near, the electrode surface. However, diamond electrodes can generate oxidizing species that facilitate micropollutant degradation in the bulk water solution. These include persulfate, sulfate radicals, peroxodiphosphate, ferrate, permanganate, reactive chlorine species, hydrogen peroxide, and ozone, which have been reported during electrochemical treatment of water with diamond electrodes. Although still restricted to specialized applications, recent studies, summarized in this review, have proven the electrogeneration of these additional oxidant species to be effective. They have shown the adaptability and potential of diamond electrode-based water treatment to mitigate the presence of micropollutants in water. 相似文献
9.
M.V. Cid Alfaro A.S.J. Suiker C.V. Verhoosel R. de Borst 《European Journal of Mechanics - A/Solids》2010,29(2):119-131
Discrete microscale fracture processes in thin fibre-epoxy layers are connected to a mesoscale traction-separation law through a numerical homogenization framework. The microscale fracture processes are studied with the finite element method, where cracking within the epoxy and debonding between fibres and epoxy is simulated by placing interface elements furnished with a mixed-mode interface damage model in between the continuum elements modelling the fibres and epoxy. It is demonstrated how the effective traction-separation response and the corresponding microscale fracture patterns under mesoscale tensile conditions depend on the sample size, the fibre volume fraction and the presence of imperfections. 相似文献
10.
Serxio I. Arias-Barros Antonio Cid Luis García-Río Juan C. Mejuto Jorge Morales 《Colloid and polymer science》2010,288(2):217-221
The influence of different polyethylene glycol (PEG) on the percolation of the ternary system composed by sodium bis(2-ethylhexyl)
sulfosuccinate (AOT) + isooctane + water has been studied. The additives used were chosen on the basis of its chain length
(the number of polymeric units). In all cases, we observed a decrease in the percolation threshold on increasing the amount
of PEG added to the AOT microemulsions. We observed a correlation between the effect exerted by the additive upon the percolation
temperature and its chain length. Moreover, a relationship between the percolation temperature and the additive partition
coefficient between 1-octanol and water (logP) was found. Both of them proved the importance of the inclusion of the additives into the microemulsion interface to explain
their influence upon the percolative phenomenon. Such inclusion modified the properties of the AOT film, facilitating the
exchange of matter between droplets. 相似文献