全文获取类型
收费全文 | 350篇 |
免费 | 7篇 |
国内免费 | 4篇 |
专业分类
化学 | 208篇 |
晶体学 | 2篇 |
力学 | 29篇 |
数学 | 71篇 |
物理学 | 51篇 |
出版年
2023年 | 1篇 |
2022年 | 3篇 |
2021年 | 9篇 |
2020年 | 4篇 |
2019年 | 5篇 |
2018年 | 8篇 |
2017年 | 7篇 |
2016年 | 7篇 |
2015年 | 7篇 |
2014年 | 16篇 |
2013年 | 28篇 |
2012年 | 17篇 |
2011年 | 32篇 |
2010年 | 16篇 |
2009年 | 17篇 |
2008年 | 27篇 |
2007年 | 27篇 |
2006年 | 21篇 |
2005年 | 15篇 |
2004年 | 9篇 |
2003年 | 19篇 |
2002年 | 11篇 |
2001年 | 8篇 |
2000年 | 2篇 |
1999年 | 4篇 |
1998年 | 5篇 |
1997年 | 1篇 |
1996年 | 3篇 |
1995年 | 4篇 |
1994年 | 1篇 |
1992年 | 1篇 |
1989年 | 1篇 |
1986年 | 1篇 |
1985年 | 3篇 |
1984年 | 1篇 |
1982年 | 4篇 |
1981年 | 3篇 |
1980年 | 2篇 |
1979年 | 3篇 |
1978年 | 3篇 |
1976年 | 2篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有361条查询结果,搜索用时 109 毫秒
1.
The kinetics of hydrolysis of a series of N-acylsulfamate esters p-XC6H4OSO2NHCOR as models for more complex, biologically important compounds has been examined. Structure-reactivity, solvent-reactivity, thermodynamic data, etc. support a bimolecular mechanism involving water in the transition state (TS). 相似文献
2.
Colette Deschamps-Vallet Jean-Baptiste Ilots Michle Meyer-Dayan Darius Molho 《Journal of heterocyclic chemistry》1982,19(1):97-101
3-Phenyl-1-benzopyrylium percholorates 1a, 1i react exculusively at C-2 with ethanol and isopropyl alcohol, affording mixed acetals 2a, 3a, 3i . Aqueous ammonia gives symmetrical secondary amines 4a, 4b or bis(3-phenyl-2H-1-benzopyran-2-yl)amines, while with aqueous aliphatic amines (40%) bis-acetals 5a, 5b or 2,2′-oxy-bis(3-phenyl-2H-1-benzopyrans) are characterized. In some other acidic conditions, 5a and 5b are also obtained. 相似文献
3.
The cis,cis,cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)-cyclopentane-[PdCl(eta3-C3H5)]2 system catalyses the coupling of aryl halides with alkynes with very high ratios of substrates-catalyst in good yields; a turnover number of 2600000 can be obtained for the reaction of 4-trifluoromethylbromobenzene with phenylacetylene in the presence of this catalyst. 相似文献
4.
Cline Schneider Frdric Doucet Stanislav Strekopytov Christopher Exley 《Polyhedron》2004,23(18):3185-3191
Hydroxyaluminosilicates (HAS) are critical secondary mineral phases in the biogeochemical cycle of aluminium. They are formed from the reaction of silicic acid (Si(OH)4) with an aluminium hydroxide template and act as a geochemical control of the biological availability of Al. There are two main forms of HAS which we have called HASA and HASB and which of these will predominate will depend upon the Si(OH)4 to Al ratio in any one environment. In all but the most heavily weathered environments or those undergoing a progressive acidification Si(OH)4 will be present in significant excess to Al and HASB will be the dominant secondary mineral phase. We have tried to determine the solubility of HASB(s) so that its contribution to Al solubility control might be compared with other secondary minerals such as Al(OH)3(gibbsite). In preliminary experiments, the dissolution of HASB(s) was found to be non-congruent with almost no Al being released during 18 months ageing. We then demonstrated that HASB(s) was significantly less soluble than Al(OH)3(s) prepared under identical experimental conditions. We have used this information to describe a solubility expression for HASB(s) at a predefined quasi-equibrium and to calculate a solubility constant.
K*Al2Si2O5(OH)4=[Al2O4+][SiO2]2[OH-]4