全文获取类型
收费全文 | 252篇 |
免费 | 4篇 |
专业分类
化学 | 172篇 |
晶体学 | 9篇 |
力学 | 7篇 |
数学 | 23篇 |
物理学 | 45篇 |
出版年
2022年 | 5篇 |
2021年 | 6篇 |
2020年 | 6篇 |
2019年 | 11篇 |
2018年 | 5篇 |
2017年 | 8篇 |
2016年 | 8篇 |
2015年 | 2篇 |
2014年 | 2篇 |
2013年 | 17篇 |
2012年 | 18篇 |
2011年 | 11篇 |
2010年 | 11篇 |
2009年 | 6篇 |
2008年 | 9篇 |
2007年 | 3篇 |
2006年 | 10篇 |
2005年 | 8篇 |
2004年 | 10篇 |
2003年 | 7篇 |
2002年 | 11篇 |
2001年 | 2篇 |
2000年 | 4篇 |
1999年 | 2篇 |
1997年 | 3篇 |
1995年 | 2篇 |
1993年 | 2篇 |
1992年 | 3篇 |
1988年 | 2篇 |
1986年 | 3篇 |
1985年 | 5篇 |
1984年 | 5篇 |
1983年 | 3篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1977年 | 2篇 |
1976年 | 2篇 |
1973年 | 5篇 |
1971年 | 1篇 |
1967年 | 3篇 |
1965年 | 1篇 |
1963年 | 1篇 |
1961年 | 2篇 |
1960年 | 2篇 |
1955年 | 1篇 |
1948年 | 1篇 |
1946年 | 1篇 |
1945年 | 2篇 |
1944年 | 1篇 |
1943年 | 4篇 |
排序方式: 共有256条查询结果,搜索用时 0 毫秒
1.
Summary The enzymes a-amylase, invertase and glucoamylase were immobilized on acid activated montmorillonite using two techniques,
viz. adsorption and covalent binding, and their activities were tested in a batch and packed-bed reactor and were compared. The
packed-bed reactor showed an improved performance for all immobilized enzymes, which was attributed to lowering of diffusional
restrictions to mass transfer. Lower activity in case of batch reactor for immobilized invertase was due to a combined effect
of loss of native conformation of enzyme on account of immobilization and mass transfer resistances due to improper diffusion
of substrate to the active site of enzyme. For immobilized glucoamylase, the packed-bed reactor demonstrated exceptionally
high activity that was very close to the free enzyme. Covalently bound glucoamylase showed higher activity than the free enzyme. 相似文献
2.
3.
Thioacetals and thioketals of various aldehydes and ketones were obtained directly from carbonyl compounds or by a transthioacetalisation process from cyclic O,O-acetals in the presence of dithiols and a catalytic amount of tetrabutylammonium tribromide (TBATB). Chemoselective thioacetalisation of aromatic aldehydes containing an electron-donating group in the presence of an aldehyde containing an electron-withdrawing group, aldehydes in the presence of ketones, aliphatic cyclic ketones in the presence of aromatic ketones and less hindered ketones in the presence of more hindered ketones have been achieved. A cyclic acetal containing an electron-donating group has been chemoselectively transthioacetalised in the presence of an acetal having an electron-withdrawing substituent. These selectivities are due to the intrinsic reactivity of the substrate themselves and are independent of the catalyst and reaction conditions. Shorter reaction times, mild reaction conditions, stability of acid sensitive protecting groups, high efficiencies, facile isolation of the desired products and the catalytic nature of the reagent are the attractive features of the present method. 相似文献
4.
S. P. Hasilkar N. Gopinath Keshav Chander S. G. Marathe H. C. Jain 《Journal of Radioanalytical and Nuclear Chemistry》1988,122(1):69-73
A method based on the complexometric titration of thorium using ethylene diaminetetra-acetic acid (EDTA) as complexant has been developed for the determination of thorium in thorium-plutonium solution without resorting to prior separation of plutonium. Plutonium in the form of Pu(VI) does not affect the thorium determination when present up to 10% in thorium—plutonium solution. For oxidation of plutonium to Pu(VI), HClO4 or AgO was used. HClO4 is preferred. The thorium values obtained without prior separation of plutonium are compared with those obtained after separating plutonium by anion exchange technique. A precision of ±0.5% has been obtained for 5–10 mg of thorium in the aliquot. 相似文献
5.
Pyrrolidine dithio carbamate (pdtc) cobalt(III) chelate has been used as a coprecipitation matrix for obtaining preconcentration factors of 100 or more for
analytical estimation of trace metals in natural waters. This chelate, suitable for bivalent and trivalent ions, crystallizes
as dark green crystals in monoclinic space group C2/c with unit cell parametersa = 28.89 ?,b = 14.39 ?,c = 16.17 ? andΒ = 104.2‡. X-ray crystallographic analysis of these crystals reveals that threepdtc are coordinated to a Co
0
3 +
atom through their sulphur atoms, the six sulphur atoms forming a distorted octahedra around the metal atom at an average
distance of 2.26 ?. The thiocarbamate part of the ligands is nearly planar but the pyrrolidine rings are puckered. 相似文献
6.
Thirunavukkarasu K Thirumoorthy K Libuda J Gopinath CS 《The journal of physical chemistry. B》2005,109(27):13272-13282
Nitric oxide (NO) reduction with carbon monoxide (CO) on the Pd(111) surface was studied under isothermal conditions by molecular beam techniques as a function of temperature, NO:CO beam composition, and beam flux. Systematic experiments were performed under transient and steady state conditions. Displacement of adsorbed CO by NO in the transient state of the reaction was observed at temperatures between 375 and 475 K for all the NO:CO compositions studied. NO accumulation occurs on Pd(111) surface under steady state conditions, below 475 K, due to stronger chemisorption of NO. The steady state reaction rates attain a maximum at about 475 K, nearly independent of beam composition. N2 was found to be the major product of the reduction, along with a minor production of N2O. The production of N2 and N2O indicates molecular and dissociative adsorption of NO on Pd(111) at temperatures up to 525 K. Postreaction TPD measurements were performed in order to determine the nitrogen coverage under steady-state conditions. Finally, the results are discussed with respect to the rate-controlling character of the different elementary steps of the reaction system. 相似文献
7.
8.
TBDMS, THP, and DMT ethers are efficiently deprotected with tetrabutylammonium tribromide in methanol. The apparent order of stability of different protecting group is phenolic TBDMS > 1 degrees OTBDPS > 2 degrees OTBDMS > 2 degrees OTHP > 1 degrees OTHP > 1 degrees OTBDMS > 1 degrees ODMT. TBDMS ether has been cleaved selectively in the presence of isopropylidine, Bn, Ac, Bz, THP, and TBDPS groups. This method is high yielding, fast, clean, safe, cost-effective, and therefore most suitable for practical organic synthesis. 相似文献
9.
10.
Rasitha Manha Veedu Niklas Niemeyer Dr. Nils Bäumer Dr. Krishnan Kartha Kalathil Prof. Dr. Johannes Neugebauer Prof. Dr. Gustavo Fernández 《Angewandte Chemie (International ed. in English)》2023,62(49):e202314211
The functionalization of π-conjugated scaffolds with sterically demanding substituents is a widely used tactic to suppress cofacial (H-type) stacking interactions, which may even inhibit self-assembly. Contrary to expectations, we demonstrate herein that increasing steric effects can result in an enhanced thermodynamic stability of H-type supramolecular polymers. In our approach, we have investigated two boron dipyrromethene (BODIPY) dyes with bulky phenyl ( 2 ) and mesityl ( 3 ) meso-substituents and compared their self-assembly in nonpolar media with that of a parent meso-methyl BODIPY 1 lacking bulky groups. While the enhanced steric demand induces pathway complexity, the superior thermodynamic stability of the H-type pathways can be rationalized in terms of additional enthalpic gain arising from intermolecular C−H⋅⋅⋅F−B interactions of the orthogonally arranged aromatic substituents, which overrule their inherent steric demand. Our findings underline the importance of balancing competing non-covalent interactions in self-assembly. 相似文献