全文获取类型
收费全文 | 85篇 |
免费 | 0篇 |
专业分类
化学 | 84篇 |
物理学 | 1篇 |
出版年
2021年 | 1篇 |
2017年 | 1篇 |
2015年 | 3篇 |
2014年 | 2篇 |
2013年 | 8篇 |
2012年 | 4篇 |
2011年 | 5篇 |
2010年 | 2篇 |
2009年 | 3篇 |
2008年 | 1篇 |
2007年 | 2篇 |
2006年 | 8篇 |
2005年 | 6篇 |
2004年 | 4篇 |
2003年 | 6篇 |
2002年 | 4篇 |
2001年 | 3篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1996年 | 1篇 |
1992年 | 1篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1988年 | 1篇 |
1986年 | 1篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 3篇 |
1980年 | 2篇 |
1978年 | 2篇 |
排序方式: 共有85条查询结果,搜索用时 187 毫秒
1.
U.Biader Ceipidor M. Tomassetti F. Bonati R. Curini G. Dascenzo 《Thermochimica Acta》1983,63(1):59-66
Complexes of general formula M[H2B(Me2pz)2]2, [where M = Co(II), Ni(II), Cu(II), and Zn(II)] are characterized by thermal analysis and complementary techniques. Mixtures of boron and metal oxides are found as final residues. Relative thermal stability (Ni > Cu > Co = Zn) and thermal behaviour are discussed. Melting and sublimation data are compared with those referred to in the literature. 相似文献
2.
M. Curini A. Bianchi F. Epifano R. Bruni L. Torta A. Zambonelli 《Chemistry of Natural Compounds》2003,39(2):191-194
Essential oils of Erigeron canadensis L. and Myrtus communis L. were tested in vitro as growth inhibitors against phytopathogenic fungi Rhizoctonia solani Kuhn, Fusarium solani (Mart.) Sacc. and Colletotrichum lindemuthianum (Sacc. & Magn.) Briosi & Cav. Both showed weak fungicidal acitivity, except the essential oil of M. communis that exerted a 60% growth inhibition against R. Solani at a dose of 1600 ppm. Microscopic observation revealed that the essential oil of M. Communis caused morphological alterations of hyphae of all fungi at 1600 ppm, while, at the same dose, only the hyphal morphology of C. Lindemuthianum was affected by the essential oil of Er. Canadensis. 相似文献
3.
Laganà A Curini R D'Ascenzo G De Leva I Faberi A Pastorini E 《Rapid communications in mass spectrometry : RCM》2003,17(10):1037-1043
A reliable, sensitive and selective liquid chromatography/tandem mass spectrometry (LC/MS/MS) method has been developed to determine four trichothecene mycotoxins (nivalenol, deoxynivalenol, fusarenon X and 3-acetyldeoxynivalenol) in maize. Sample preparation was performed by extracting the analytes with a mixture of acetonitrile and water, followed by a solid-phase extraction with Carbograph-4 cartridges as the purification step. For the LC/MS/MS analysis two interfacing systems, Turbo IonSpray (TISP) and atmospheric pressure chemical ionization (APCI), were compared in both negative and positive ion modes. LC and MS parameters were optimized to achieve better results and sensitivity. The effect of mobile phase modifiers such as ammonium acetate and formic acid on the ionization yield was also evaluated. The best results were obtained using the electrospray ionization (ESI) interface in negative ion mode and the multiple reaction monitoring mode (MRM) for the quantitation. The detection limits ranged between 10 ng/g for fusarenon X and 1.5 ng/g for deoxynivalenol. A linear working range was achieved with a standard deviation between 3 and 10% and recovery rates from the maize samples above 81%. The procedure was applied to the analysis of a set of maize samples collected from farms located in different areas of northern and central Italy. The investigated samples turned out to be contaminated primarily with deoxynivalenol and, to a minor extent, with its derivatives. 相似文献
4.
A specific method for measuring concentrations of cortisol in serum, by preliminary isolation on a "minicolumn" followed by elution and determination by liquid chromatography, is described. This assay requires only 500 microl of serum. The limit of determination of cortisol was found to be 5 microg l . The analytical recovery of cortisol added to serum ranged from 98 to 102%. The coefficients of variation ranged from 2.4 to 3.4% (within-day) and from 3.6 to 8.8% (day-to-day), depending on the cortisol concentration. The method compares well with a commonly used radioimmunological method. 相似文献
5.
Marchese S Curini R Gentili A Perret D Rocca LM 《Rapid communications in mass spectrometry : RCM》2004,18(3):265-272
A simple and rapid method using reversed-phase liquid chromatography/tandem mass spectrometry (LC/MS/MS) for the simultaneous determination of the urinary metabolites of benzene, toluene, xylene and styrene in human urine specimens and standard solutions is described. A hybrid quadrupole/time-of-flight (QqTOF) mass spectrometer was compared for the determination of metabolite of aromatic solvents in urine samples. The metabolites selected were: trans,trans-muconic acid, hippuric acid, o-, m- and p-methylhippuric acid and phenylglyoxylic acid. The compounds were well separated from each other on narrow-bore 1-mm i.d. reversed-phase LC C-18 columns. Average recoveries for loading 100 microL of urine samples varied from 88-110% and the quantification limits were less than 30 ng/mL for each analyte (3 ng/mL for trans,trans-muconic acid). The qualitative information obtained (mass accuracy, resolution and full-scan spectra) with the QqTOF mass spectrometer allows a secure identification of analytes in biological matrices. 相似文献
6.
[reaction: see text] Ytterbium triflate was shown to be an effective catalyst in promoting the synthesis of either isopropyl esters or free alpha-hydroxy-arylacetic acids from substituted aromatic glyoxals and aryl methyl ketones, respectively. The reaction to provide acids starting from differently substituted ketones was carried out by an environmentally friendly method using an aqueous medium as a solvent and giving the adducts in 78-99% yield without any further purification after the usual workup. 相似文献
7.
Massimo Curini Francesco Epifano Maria Carla Marcotullio Ornelio Rosati Monia Rossi André Tsadjout 《合成通讯》2013,43(17):3181-3187
Layered zirconium hydrogen phosphonate exchanged with the potassium ion was found to be an efficient heterogeneous catalyst for the hydrolysis of sterically hindered phenolic silyl ethers. 相似文献
8.
Nera Cagnoli Paolo Ceccherelli Massimo Curini Maria Carla Marcotullio Ernest Wenkert 《合成通讯》2013,43(11):1261-1271
Copper oxide-catalyzed decomposition of 1-diazoacetyl-1-methyl-3-methylenecyclohexanes produces strained tricycles whose reduction or hydrolysis affords 6-bicyclo[3.2.1]octanones. 相似文献
9.
Manuel Sergi Natalia Battista Camilla Montesano Roberta Curini Mauro Maccarrone Dario Compagnone 《Analytical and bioanalytical chemistry》2013,405(2-3):785-793
Endocannabinoids (ECs) are endogenous compounds that interact with type-1 and type-2 cannabinoid receptors (CB1 and CB2), as well as non-cannabinoid receptors. The multitude of roles attributed to ECs makes them an emerging target of pharmacotherapy for a number of disparate diseases. Here a high-throughput bioanalytical method based on micro SPE (μ-SPE) followed by LC-MS/MS analysis for the simultaneous determination of the two major endocannabinoids 2-arachidonoylglycerol (2-AG) and N-arachidonoylethanolamine (anandamide, AEA) in human plasma is presented. The chromatographic conditions obtained with the fused-core column allowed a good separation in 10 min also of the AG isomers. A very simple and reliable extraction has been optimised by means of C18-modified tips: it requires only 100 μL of plasma and allows the use of minimal volumes of organic solvent. The present method allows a rapid and effective clean-up, which also minimises the isomerisation of 2-AG. The whole procedure has been validated following the FDA guidelines for bioanalytical methods validation: the satisfactory recovery values, the negligible matrix effect and the good values of accuracy and reproducibility make it a simple and high-throughput analytical tool for clinical and biochemical studies on endocannabinoid signaling in humans. Figure
Determination of the two major endocannabinoids in human plasma by μ-SPE followed by HPLC-MS/MS 相似文献
10.