全文获取类型
收费全文 | 121篇 |
免费 | 3篇 |
专业分类
化学 | 94篇 |
力学 | 1篇 |
物理学 | 29篇 |
出版年
2022年 | 1篇 |
2021年 | 4篇 |
2020年 | 3篇 |
2019年 | 3篇 |
2018年 | 3篇 |
2016年 | 3篇 |
2015年 | 3篇 |
2014年 | 6篇 |
2013年 | 19篇 |
2012年 | 2篇 |
2011年 | 7篇 |
2010年 | 8篇 |
2009年 | 4篇 |
2008年 | 8篇 |
2007年 | 13篇 |
2006年 | 3篇 |
2005年 | 11篇 |
2004年 | 2篇 |
2003年 | 5篇 |
2002年 | 1篇 |
2001年 | 1篇 |
2000年 | 1篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1992年 | 3篇 |
1990年 | 2篇 |
1984年 | 2篇 |
排序方式: 共有124条查询结果,搜索用时 46 毫秒
1.
Fathy Abdel‐Kader Amer Metwally Hammouda Abdel‐Aziz Sayed El‐Ahl Bakr Fathy Abdel‐Wahab 《中国化学会会志》2007,54(6):1543-1552
Treatment of heterocyclic β‐ketonitriles 1a,b with hydrazine hydrate and phenylhydrazine afforded the hydrazine derivatives 2a‐d which cyclized in PPA into pyrrolo[3,4‐c]pyrazoles 3a‐d. Reaction of 1a,b with cyanoacetohydrazide furnished the cyanoacetyl pyrrolo[3,4‐c]pyrazoles 4a,b. The hydrazine 2c reacted with β‐diketone and β‐ketoesters to afford pyrazolyl‐pyrrolines 5‐7. Also the later hydrazine reacted with some D‐aldoses and aceteophenone to give the corresponding hydrazones 10‐12 and hydrazine carboxamide derivatives 15a,b respectively. 相似文献
2.
New methods for determination of cinnarizine in mixture with piracetam by spectrodensitometry, spectrophotometry, and liquid chromatography 总被引:1,自引:0,他引:1
Four new methods were developed and validated for the determination of cinnarizine HCl in its binary mixture with piracetam in pure and pharmaceutical preparations. The first one was a densitometric analysis that provides a simple and rapid method for the separation and quantification of cinnarizine HCI. The method depends on the quantitative densitometric evaluation of thin-layer chromatograms of cinnarizine HCI at 252 nm over concentration range of 1-6 microg/spot, with a mean accuracy of 100.05 +/- 0.91%. The second method was determination of the drug using a colorimetric method that utilizes the reaction of 3-methyl-benzothiazolin-2-one in the presence of FeCl3 as an oxidant. The green color of the resulting product was measured at 630 nm over concentration range 10-40 microg/mL, with a mean accuracy of 100.10 +/- 1.13%. The third method was a direct spectrophotometric determination of cinnarizine HCI at 252 nm over the concentration range 7-20 microg/mL, while piracetam was determined by derivative ratio spectrophotometry at 221.6 nm over concentration range 5-30 microg/mL, with a mean accuracy of 100.14 +/- 0.79 and 100.26 +/- 1.24% for cinnarizine HCI and piracetam, respectively. The last method was a liquid chromatography analysis of both cinnarizine HCI and piracetam, depending on quantitative evaluation of chromatograms of cinnarizine HCI and piracetam at 252 and 212 nm, respectively, over the concentration range 10-200 microg/mL for cinnarizine HCI and 20-500 microg/mL for piracetam, with a mean accuracy of 100.03 +/- 0.89 and 100.40 +/- 0.94% for cinnarizine HCI and piracetam, respectively. The proposed procedures were checked using laboratory-prepared mixtures and successfully applied for the analysis of their pharmaceutical preparations. The validity of the proposed procedures was further assessed by applying the standard addition technique. Recoveries were quantitative, and the results obtained agreed with those obtained by other reported methods. 相似文献
3.
M. S. Metwally 《Reaction Kinetics and Catalysis Letters》1992,47(2):319-326
A kinetic study of solvent effect on sulfonated resin catalyzed hydrolysis of ethyl propionate has been made in water-acetone, water-dioxane, water-DMF and water-DMSO solvent mixtures of varying compositions, at different temperatures. Specific rate constants (kr) were found to be a first order and decreased with increasing amount of organic co-solvent in the media. The variation in rates as well as the activation parameters have been interpreted on the basis of specific solvation ion and dielectric properties of the medium.
, , — -, -, - — . . .相似文献
4.
A. Abdel Razik M. S. Metwally M. F. El-Hadi M. A. El Wardany 《Reaction Kinetics and Catalysis Letters》1992,48(1):279-290
The rates of hydrolysis of seven acetate esters substituted in the alkyl group have been studied in the presence of a sulfonated cation exchange resin in 70% aqueous acetone solution. the slower hydrolysis rates with increasing size of substituent are related to increasing steric influence, as determined by decreasing values of the steric substituent parameter, Es. The efficiency of the resin catalyst is related to the entropy of substituents. Influence caused by steric hindrance on reaction rates accounts satisfactorily for observed variations of the enthalpies and entropies of activation with alkyl group substituents. The entropy, Sx, values increase in the order: n-octyl-
, , 70%- . , , ES. . , . , S*, : --<-<, .相似文献
5.
R. P. Gardner W. Zhang W. A. Metwally 《Journal of Radioanalytical and Nuclear Chemistry》2005,264(1):221-228
Summary {\rtf1\ansi\ansicpg1250\deff0\deflang1038\deflangfe1038\deftab708{\fonttbl{\f0\froman\fprq2\fcharset238{\*\fname Times New Roman;}Times New Roman CE;}}
\viewkind4\uc1\pard\f0\fs24 The Center for Engineering Applications of Radioisotopes (CEAR) has been working for about ten years on the Monte Carlo - Library Least-Squares (MCLLS) approach for treating the nonlinear inverse analysis problem for PGNAA bulk analysis. This approach consists essentially of using Monte Carlo simulation to generate the libraries of all the elements to be analyzed plus any other required libraries. These libraries are then used in the linear Library Least-Squares (LLS) approach with unknown sample spectra to analyze for all elements in the sample. The other libraries include all sources of background which includes: (1) gamma-rays emitted by the neutron source, (2) prompt gamma-rays produced in the analyzer construction materials, (3) natural gamma-rays from K-40 and the uranium and thorium decay chains, and (4) prompt and decay gamma-rays produced in the NaI detector by neutron activation. A number of unforeseen problems have arisen in pursuing this approach including: (1) the neutron activation of the most common detector (NaI) used in bulk analysis PGNAA systems, (2) the nonlinearity of this detector, and (3) difficulties in obtaining detector response functions for this (and other) detectors. These problems have been addressed by CEAR recently and have either been solved or are almost solved at the present time. We have now finished the development of Monte Carlo simulation for all of the libraries except the prompt gamma-ray library from the activation of the NaI detector. We must first determine a treatment for the coincidence schemes for Na and particularly I to complete the Monte Carlo simulation of this last library.
\par } 相似文献
6.
Metwally Nadia H. Abdelrazek Fathy M. Eldaly Salwa M. 《Research on Chemical Intermediates》2016,42(2):1071-1089
Research on Chemical Intermediates - The starting 3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxopropanenitrile (1) reacts with phenyl isothiocyanate and ethyl bromoacetate to give the corresponding... 相似文献
7.
M. A. Metwally Bakr F. Abdel-Wahab M. Koketsu 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):3038-3074
The data on the methods of synthesis and chemical properties of the thiophene ring in 2-acetylthiophenes published over the last several years until mid 2007 are reviewed for the first time. Many of the synthesized compounds exhibit interesting biological activity in various fields and are used in the production of pharmaceuticals, agrochemicals, dyes, and electrophotogeneratoragents. 相似文献
8.
9.
Nadia Hanafy Metwally 《合成通讯》2013,43(3):398-405
2-Keto-3-mercaptocinchoninic acid derivatives 1a and b react with Schiff's bases 2a–d in toluene at refluxing temperature to give thiazino[6,5-c]quinoline derivatives 4a–h. Also, refluxing of 1a and b with arylazomalononitriles 5a–d in acetic acid afforded the thiazolo[6,5-c]quinoline derivatives 7a–d. The structure of all the newly synthesized products was confirmed based on elemental and spectral data. 相似文献
10.
S. S. Metwally R. R. Ayoub H. F. Aly 《Journal of Radioanalytical and Nuclear Chemistry》2014,302(1):441-449
Eggshell material was used as low-cost and eco-friendly biosorbent for removal of 134Cs, 60Co and 152+154Eu radionuclides from aqueous solution. The eggshell material was calcined at 500 and 800 °C, and then characterized. Comparative studies on the natural and calcined eggshell for sorption of the three radionuclides were carried out. It was found that, the uptake is in the order: Eu(III) > Co(II) > Cs(I). Further, column chromatography was used in separation of 134Cs, 60Co and 152+154Eu using 0.15, 0.2 and 0.5 mol/l nitric acid, respectively. Eggshell material can be considered as a promising material for separation of radionuclides from radioactive waste solution. 相似文献