全文获取类型
收费全文 | 196篇 |
免费 | 14篇 |
国内免费 | 1篇 |
专业分类
化学 | 133篇 |
晶体学 | 9篇 |
力学 | 4篇 |
数学 | 25篇 |
物理学 | 40篇 |
出版年
2024年 | 1篇 |
2022年 | 2篇 |
2021年 | 8篇 |
2020年 | 7篇 |
2019年 | 7篇 |
2018年 | 8篇 |
2017年 | 9篇 |
2016年 | 10篇 |
2015年 | 11篇 |
2014年 | 5篇 |
2013年 | 20篇 |
2012年 | 14篇 |
2011年 | 16篇 |
2010年 | 7篇 |
2009年 | 8篇 |
2008年 | 12篇 |
2007年 | 11篇 |
2006年 | 6篇 |
2005年 | 6篇 |
2004年 | 7篇 |
2003年 | 6篇 |
2002年 | 4篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1995年 | 1篇 |
1993年 | 1篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1988年 | 1篇 |
1985年 | 1篇 |
1982年 | 2篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1970年 | 1篇 |
1968年 | 1篇 |
1966年 | 2篇 |
排序方式: 共有211条查询结果,搜索用时 15 毫秒
41.
A. M. El-Naggar F. S. M. Ahmed A. M. Abd El-Salam M. A. Radi M. S. A. Latif 《Journal of heterocyclic chemistry》1981,18(6):1203-1207
The synthesis of 6-nitrocouarrain-3-CO-amino acids and their corresponding methyl esters (II-XVII) and some dipeptide methyl esters (XVIII-XXVI) are described. 6-(N-Tosyl- or N-phthalylaminoacyl)aminocoumarin-3-carboxylic acid methyl esters (XXXIV-XL) and 3-(N-phthalyl- or N-tosylaminoacytyaminocoumarins (XLV-LVI) have been prepared via the carbodiimide and acid chloride methods. Hydrazinolysis of 3- or 6-(N-phthalylaminoacyl)aminocoumarin derivatives in tetraline gave the corresponding 3- and 6-(aminoacyl)aminocoumarins and the carboxylic acid hydrazides (XLI-LVIII), respectively. 3-(N-Tosyl-L-Val-L-Leu-)aminocoumarin (LIX) was synthesized via the azide method. Twenty four of various substituted 3- and 6-aminoacylcoumarin derivatives were found to possess specific antimicrobial activities towards different microorganisms. 相似文献
42.
M. Sakhawat Hussain Abdul Rahman Al-Arfaj M. Latif Hossain 《Transition Metal Chemistry》1990,15(4):264-269
Summary Novel mixed-ligand copper(I) complexes of general formula [TPP–Cu–(L)Cl] or [TPPhos–Cu–(L)Cl], where TPP=triphenylphosphine, TPPhos=triphenylphosphate and L=imidazolidine-2-thione [Imt],N-propylimidazolidice-2-thione [PrImt],N-i-propylimidazolidine-2-thione [iPrImt], and 1,3-diazinine-2-thione [Diaz] and bis coniplexes of formula [(L)2CuCl] where L=[PrImt] and [iPrImt] have been prepared and characterized by electronic, vibrational and n.m.r. spectroscopy. The spectral data are consistent with S-donation of thiones. The magnitude of upfield shift in13Cn.m.r. of the thionreide carbon on complexation has been interpreted in terms of coordination geometry around the metal stoms. X-ray structure analysis agrees with the conclusions from the spectroscopic measurements. The structure of [(PrImt)2CuCl] revealed three-coordinated copper(I) with crystal data:a=14.106(4),b=14.380(2),c=19.024(3) A, =108.8(2)°,z=8 and space group P2/c. 相似文献
43.
M. Sakhawat Hussain M. Latif Hossain Abderehman Al-Arfaj 《Transition Metal Chemistry》1990,15(2):120-125
Summary Novel mixed-ligand complexes of Ag1 and Au1 containing triphenylphosphine (TPP) and heterocyclic thiones, of general formula [TPP–M–L]Cl and [(TPP)2–M–L]Cl, where L=imidazolidine-2-thione (Imt), 1,3-diazinine-2-thione (Diaz) or N-isopropylimidazolidine-2-thione (iPrImt) have been prepared. The spectroscopic data are consistent with S-donation in all complexes. The magnitude of high-field shift in carbon-13 n.m.r. of the thioureide carbon on complexation is interpreted in terms of coordination geometry around the metal atoms. The mixed-ligand complexes are structurally similar to some of the commonly used antiarthritic Au1 drugs and are thus potentially useful in chemotherapy. 相似文献
44.
A method was described for the determination of the elements Cr, Mn, Fe, Co, Ni, Cu, Cd, Pb, and Bi in waters by flame atomic absorption spectrometry (FAAS) after separation and preconcentration on Amberlite XAD-16 resin with sodium tetraborate using a chromatographic column. Parameters influencing the analytical performance, including pH and the volume of sample, amount of analyte and interfering effect of co-existing ions, were studied in detail. The recovery values were quantitative (> or = 95%), and the relative standard deviation (RSD) and detection limit (DL) varied in the range of 1.1-2.4% (n=10) and 0.002-0.177 microg m(-1) (3s, n=20), respectively. After being optimized, the proposed method was applied to the drinking water, waste water and artificial sea water samples. Recovery values of the elements investigated, were quantitative for tap water and synthetic sea water, except for Mn, Co and Ni (including also Cd for synthetic sea water). Recovery values of Cd, Pb, Cu and Co were found to be 95, 102, < or = 87, and < or = 83%, respectively, for the waste water samples. 相似文献
45.
Multi-element determination of trace elements in urine and dialysis solutions by atomic absorption spectrometry has been investigated. Coprecipitation with samarium hydroxide was used for preconcentration of trace elements and elimination of matrix elements. To 10 ml of each sample was added 500 μl of 2 mg ml−1 samarium solutions; the pH was then adjusted to 12.2 in order to collect trace heavy metals on samarium hydroxide. The precipitate was separated by centrifugation and dissolved in 1 ml of 1 mol l−1 HNO3. Coprecipitation parameters and matrix effects are discussed. The precision, based on replicate analysis, is around 5% for the analytes, and recovery is quantitative, based on analysis of spiked samples and solutions including matrix components. The time required for the coprecipitation and determination was about 30 min. 相似文献
46.
Dr. Akiko Nakamura Dr. Marwa Abdel Latif Prof. Paul A. Deck Prof. Neal Castagnoli Jr. Prof. James M. Tanko 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(4):823-829
Mechanistic studies with 5-ethyl-3-methyllumiflavinium (Fl+) perchlorate, a biomimetic model for flavoenzyme monoamine oxidase B (MAO-B) catalysis, and the tertiary, allyl amine 1-methyl-4-(1-methyl-1 H-pyrrol-2-yl)-1,2,3,6-tetrahydropyridine (MMTP) reveal that proton-coupled electron transfer (PCET) may be an important pathway for MAO catalysis. The first step involves a single-electron transfer (SET) leading to the free radicals Fl. and MMTP., the latter produced by deprotonation of the initially formed and highly acidic MMTP.+. Molecular oxygen (O2) is found to play a hitherto unrecognized role in the early steps of the oxidation. MMTP and several structurally similar tertiary amines are the only tertiary amines oxidized by MAO, and their structural/electronic properties provide the key to understanding this behavior. A general hypothesis about the role of SET in MAO catalysis, and the recognition that PCET occurs with appropriately substituted substrates is presented. 相似文献
47.
48.
The main purpose of this note is to show that the question posed in the paper [1] of D. P. Sinha D. P. and A. K. Karn (see the very end of that paper) has a negative answer, and that the answer could have been obtained, essentially, in 1985 after the papers [2], [3] by the author appeared in 1982 and 1985, respectively. 相似文献
49.
Mukhtiar Ahmed Muhammad Nazim Lakhan Altaf Hussain Shar Irum Zehra Abdul Hanan Irfan Ali Muhammad Ahsan Latif Kishore Chand Asif Ali Jun Wang 《印度化学会志》2022,99(1):100281
Active nanocomposites synthesized by the electrochemical approach play a vital role in energy generation, conversion, and storage technologies. Recently, scientists began to explore the use of earth-rich transition metal-based materials to replace precious metal-based catalysts. Transition metals (TMs) based nickel (Ni) and their pnictides compounds such as phosphides and selenides exhibit good activity for hydrogen evaluation reaction (HER) and the entire water electrolysis process. In this study, we first prepared Ni(OH)2 and grown its layer on Ni foam (NF) and treated it with selenide (Se) and phosphide (P) then nickel-based selenide-phosphide catalyst (Ni–P–Se) was prepared by simultaneous selenization and phosphidation process for the first time. The as-obtained composite was then analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM), elemental mapping and transmission electron microscope (TEM) means to study the composition, structure, and micro-morphology of materials. Furthermore, we also observed electrocatalytic water splitting activity using electrochemical cell. The results of electrochemical tests depicted that the selenization and phosphidation treatments significantly enhanced the electrocatalytic HER activity of the starting materials. The overpotentials required for Ni–P–Se to reach 10 ?mA ?cm?2 and 100 ?mA ?cm?2 were only 242 ?mV and 282 ?mV. The Tafel slope of Ni–P–Se is 151 ?mV dec?1, which is lower than that of nickel phosphide, selenide, and hydroxide indicating that selenide-phosphide enhances the HER reaction kinetics of the material, which in turn increases hydrogen output rate as compared with previous studies. 相似文献
50.
Muhammad Amer Latif Sever Silvestru Dragomir Ebrahim Momoniat 《Journal of Applied Analysis & Computation》2017,7(3):795-813
In this paper, a new weighted identity involving harmonically symmetric functions and differentiable functions is established. By using the notion of harmonic symmetricity, harmonic convexity and some auxiliary results, some new Fej\''{e}r type integral inequalities are presented. Applications to special means of positive real numbers are given as well. 相似文献