全文获取类型
收费全文 | 2941篇 |
免费 | 39篇 |
国内免费 | 17篇 |
专业分类
化学 | 1713篇 |
晶体学 | 28篇 |
力学 | 198篇 |
数学 | 539篇 |
物理学 | 519篇 |
出版年
2020年 | 20篇 |
2019年 | 20篇 |
2018年 | 24篇 |
2017年 | 25篇 |
2016年 | 35篇 |
2015年 | 35篇 |
2014年 | 32篇 |
2013年 | 138篇 |
2012年 | 96篇 |
2011年 | 123篇 |
2010年 | 67篇 |
2009年 | 83篇 |
2008年 | 122篇 |
2007年 | 123篇 |
2006年 | 115篇 |
2005年 | 123篇 |
2004年 | 121篇 |
2003年 | 89篇 |
2002年 | 94篇 |
2001年 | 60篇 |
2000年 | 53篇 |
1999年 | 61篇 |
1998年 | 36篇 |
1997年 | 39篇 |
1996年 | 43篇 |
1995年 | 31篇 |
1994年 | 40篇 |
1993年 | 26篇 |
1992年 | 42篇 |
1991年 | 30篇 |
1990年 | 34篇 |
1989年 | 43篇 |
1988年 | 21篇 |
1987年 | 29篇 |
1986年 | 38篇 |
1985年 | 52篇 |
1984年 | 69篇 |
1983年 | 45篇 |
1982年 | 52篇 |
1981年 | 64篇 |
1980年 | 45篇 |
1979年 | 58篇 |
1978年 | 46篇 |
1977年 | 56篇 |
1976年 | 37篇 |
1975年 | 48篇 |
1974年 | 50篇 |
1973年 | 59篇 |
1972年 | 33篇 |
1970年 | 27篇 |
排序方式: 共有2997条查询结果,搜索用时 571 毫秒
121.
Catherine D. Clark Morton Z. Hoffman D. Paul Rillema Quinto G. Mulazzani 《Journal of photochemistry and photobiology. A, Chemistry》1997,110(3):285-290
The photophysics of three complexes of the form Ru(bpy)3−(pypm)2+ (where bpy2,2′-bipyridine, pypm 2-(2′-pyridyl)pyrimidine and P=1, 2 or 3) was examined in H2O, propylene carbonate, CH3CN and 4:1 (v/v) C2H5OH---CH3OH; comparison was made with the well-known photophysical behavior of Ru(bpy)32+. The lifetimes of the luminescent metal-to-ligand charge transfer (MLCT) excited states were determined as a function of temperature (between −103 and 90 °C, depending on the solvent), from which were extracted the rate constants for radiative and non-radiative decay and ΔE, the energy gap between the MLCT and metal-centered (MC) excited states. The results indicate that *Ru(bpy)2(pypm)2+ decays via a higher lying MLCT state, whereas *Ru(pypm)32+ and *Ru(pypm)2(bpy)2+ decay predominantly via the MC state. 相似文献
122.
Phospholipids (1–5 mg) are mixed with methyl heptadecanoate as an internal standard. One part of the sample is reduced with Vitride in tetrahydrofuran in a sealed tube at 50 2C for 1 hr. The reaction products are acetylated in the same tube by treatment with acetic acid-acetic anhydride at 140 °C. After 1 hr total O-acyl and after 16 additional hours glycerol are determined as the fully acetylated compounds by gas-liquid chromatography.Another part of the sample is subjected to acidic hydrolysis and total O-acyl and N-acyl groups are determined by GLC as fatty-acid methyl esters. The aqueous phase is heated to 100 °C with 6 N HCl for 72 hr and phosphorus is measured colorimetrically. 相似文献
123.
124.
Duffy DJ Quenneville J Baumbaugh TM Kitchener SA McCormick RK Dormady CN Croce TA Navabi A Stidham HD Hsu SL Guirgis GA Deng S Durig JR 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2004,60(3):659-671
Ab initio calculations are reported for three of four possible conformers of 1,3-dichloropropane. The fourth conformer, with Cs symmetry, has a predicted enthalpy difference of more than 1500 cm(-1) from the most stable conformer from each calculation regardless of the basis set used, so there is little chance of observing it. Thus, there is no evidence in the infrared or Raman spectrum of the presence of a fourth conformer. The order of stability given by the ab initio calculations is C2(GG)>C1(AG)>C2v(AA)>Cs(GG'), where A indicates the anti form for one of the CH2Cl groups and G indicates the gauche conformation for the other CH2Cl group relative to the plane of the carbon atoms. Almost every band observed can be confidently assigned to one or another of the conformers. Many observed bands proved to be of a composite nature, with several nearly coincident vibrations of different conformers contributing to the band contour. Nonetheless, a complete assignment of fundamentals is possible for the most stable C2 conformer, and 5 of the fundamentals of the C2v conformer and 13 those of the C1 conformer can be confidently assigned. 相似文献
125.
[reaction: see text] The use of 1,4-difluoro-2,5-dimethoxybenzene as a novel precursor for iterative two-directional benzyne-furan Diels-Alder reactions, using a range of 2- and 3-substituted furans, is reported. Substituted oxabenzonorbornadienes were synthesized following the initial Diels-Alder reaction, which upon ring opening under acidic conditions gave substituted naphthol derivatives. Highly substituted anthracenols were generated in the second benzyne-furan Diels-Alder reaction following acid-catalyzed isomerization of the cycloadducts. 相似文献
126.
Nabih S. Girgis Howard B. Cottam Roland K. Robins 《Journal of heterocyclic chemistry》1988,25(2):361-366
The 2′-deoxyribofuranose analog of the naturally occurring antibiotics SF-2140 and neosidomycin were prepared by the direct glycosylation of the sodium salts of the appropriate indole derivatives, with 1-chloro-2- deoxy-3,5-di-O-p-toluoyl-α-D-erythropentofuranose ( 5 ). Thus, treatment of the sodium salt of 4-methoxy-1H- indol-3-ylacetonitrile ( 4a ) with 5 provided the blocked nucleoside, 4-methoxy-1-(2-deoxy-3,5-di-O-p-toluoyl-β- D-erythropentofuranosyl)-1H-indol-3-ylacetonitrile ( 6a ), which was treated with sodium methoxide to yield the SF-2140 analog, 4-methoxy-1-(2-deoxy-β-D-erythropentofuranosyl)-1H-indol-3- ylacetonitrile ( 7a ). The neosidomycin analog ( 8 ) was prepared by treatment of the sodium salt of 1H-indol-3-ylacetonitrile ( 4b ) with 5 to obtain the blocked intermediate 1-(2-deoxy-3,5-di-O-p-toluoyl-β-D-erythropentofuranosyl) ?1H-indol-3-ylace-tonitrile ( 6b ) followed by sodium methoxide treatment to give 1-(2-deoxy-β-D-erythropentofuranosyl)-1H- indol-3-ylacetonitrile ( 7b ) and finally conversion of the nitrile function of 7b to provide 1-(2-deoxy-β-D- erythropentofuranosyl)-1H-indol-3-ylacetamide ( 8 ). In a similar manner, indole ( 9a ) and several other substituted indoles including 1H-indole-4-carbonitrile ( 9b ), 4-nitro-1H-indole ( 9c ), 4-chloro-1H-indole-2-carboxamide ( 9d ) and 4-chloro-1H-indole-2-carbonitrile ( 9e ) were each glycosylated and deprotected to provide 1-(2-deoxy-β-D-erythropentofuranosyl)-1H-indole ( 11a ), 1-(2-deoxy-β-D-erythropentofuranosyl)-1H-indole-4- carbonitrile ( 11b ), 4-nitro-1-(2-deoxy-β-D-erythropentofuranosyl)-1H-indole ( 11c ), 4-chloro-1-(2-deoxy-β-D- erythropentofuranosyl)-1H-indole-2-carboxamide ( 11d ) and 4-chloro-1-(2-deoxy-β-D-erythropentofuranosyl)- 1H-indole-2-carbonitrile ( 11e ), respectively. The 2′-deoxyadenosine analog in the indole ring system was prepared for the first time by reduction of the nitro group of 11c using palladium on carbon thus providing 4-amino-1-(2-deoxy-β-D-erythropentofuranosyl)- 1H-indole ( 16 , 1,3,7-trideaza-2′-deoxyadenosine). 相似文献
127.
128.
129.
July 1969, 528 pages, illustrated, $25.50 相似文献
130.