全文获取类型
收费全文 | 1528篇 |
免费 | 164篇 |
国内免费 | 197篇 |
专业分类
化学 | 1815篇 |
晶体学 | 2篇 |
综合类 | 18篇 |
物理学 | 54篇 |
出版年
2024年 | 2篇 |
2023年 | 20篇 |
2022年 | 40篇 |
2021年 | 45篇 |
2020年 | 85篇 |
2019年 | 49篇 |
2018年 | 47篇 |
2017年 | 42篇 |
2016年 | 77篇 |
2015年 | 57篇 |
2014年 | 66篇 |
2013年 | 161篇 |
2012年 | 60篇 |
2011年 | 76篇 |
2010年 | 66篇 |
2009年 | 60篇 |
2008年 | 74篇 |
2007年 | 84篇 |
2006年 | 87篇 |
2005年 | 71篇 |
2004年 | 87篇 |
2003年 | 116篇 |
2002年 | 48篇 |
2001年 | 37篇 |
2000年 | 43篇 |
1999年 | 28篇 |
1998年 | 41篇 |
1997年 | 45篇 |
1996年 | 34篇 |
1995年 | 28篇 |
1994年 | 39篇 |
1993年 | 22篇 |
1992年 | 15篇 |
1991年 | 4篇 |
1990年 | 7篇 |
1989年 | 6篇 |
1988年 | 4篇 |
1987年 | 6篇 |
1986年 | 2篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 1篇 |
1976年 | 1篇 |
1975年 | 1篇 |
排序方式: 共有1889条查询结果,搜索用时 514 毫秒
11.
12.
13.
V. I. Saloutin I. T. Bazyl' Z. E. Skryabina P. N. Kondrat'ev O. N. Chupakhin 《Russian Chemical Bulletin》1994,43(2):279-282
Reactions of pentafluorobenzoylpyruvic acid with amines afford the respective enamines. The intramolecular cyclization of the latter results inN-substituted 4-quinolone-2-carboxylic acids. Ammonia and triethylamine favor the cyclization of pentafluorobenzoylpyruvic acid to 2-carboxychromone.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 299–302, February, 1994. 相似文献
14.
A. O. Manyashin A. I. Fomenko V. N. Storozhenko N. T. Berberova 《Russian Journal of Electrochemistry》2003,39(11):1240-1244
Stoichiometry and kinetics of reactions of 2,6-diphenyl-4-chloropyrylium, 4-chloroflavylium, 4-bromoflavylium, and 4-iodoflavylium perchlorates with nucleophiles N,N-dimethylaniline and n-phenylenediamine are studied using cyclic voltammetry and spectroscopy. Nucleophilic substitution in these compounds proceeds via the formation of a charge-transfer complex, which converts into a radical ion pair as a result of the electron transfer. Heterolytic clevage of the C–Hal bond occurs at the stage of pyranyl (flavanyl) radical. 相似文献
15.
A novel class of platinum-based initiating systems for the ring-opening polymerization of a wide variety of heterocyclic compounds including epoxides, oxetanes, and 1,3,5-trioxane have been discovered. In addition to a platinum complex as a catalyst, a cocatalyst, consisting of a compound or polymer containing silicon-hydrogen bonds must also be present. This article reports on a preliminary survey of the scope and limitations of these new initiator systems. Particular emphasis in this article has been placed on the ring-opening polymerization of epoxides which have been studied in some detail and which proceed rapidly and exothermically at room temperature. A number of mechanistic studies have been conducted and the best current evidence suggests that polymerization proceeds by a cationic mechanism. Evidence is also presented which suggests that platinum metal colloids may function as the active initiating species. 相似文献
16.
Kazuhiko Hashimoto Sirinat Wibullucksanakul Mitsuyasu Matsuura Masahiko Okada 《Journal of polymer science. Part A, Polymer chemistry》1993,31(12):3141-3149
Ring-opening polyaddition of a saccharic acid dilactone prepared from D-glucose, D-glucaro-1,4 : 6,3-dilactone, with several alkylenediamines proceeded at room temperature with no catalyst. The resulting new polyamides carrying many pendant hydroxyl groups, poly(alkylene D-glucaramide)s, were more amorphous and hydrophilic than the corresponding nylons having no hydroxyl groups, and were hydrolyzed more easily than the latter in an acidic condition. The ring-opening ability of D-mannaro-1,4:6,3-dilactone, which was another saccharic acid dilactone obtained from D-mannitol, was found to be lower than that of the D-glucaric analogue. © 1993 John Wiley & Sons, Inc. 相似文献
17.
Zakharova L. Ya. Mirgorodskaya A. B. Zhil"tsova E. P. Kudryavtseva L. A. Konovalov A. I. 《Russian Chemical Bulletin》2004,53(7):1385-1401
The factors determining the catalytic effect of supramolecular systems on the nucleophilic substitution reactions are analyzed. The role of the structural and phase transitions of nanoaggregates in the catalytic mechanism are determined. The substrate specificity is shown for different structures of the supramolecular composition. 相似文献
18.
N. V. Moskalev M. I. Tartynova I. Yu. Bagryanskaya Yu. V. Gatilov 《Russian Chemical Bulletin》1996,45(2):462-464
Nitrobenzene,p-bromonitrobenzene,N,N-diethyl-p-nitroaniline, and 9-methyl-3nitrocarbazole undergo condensation with two moles of acetophenone in a DMSO-KOH system to form the corresponding (Z)-1,4-diphenyl-2-arylamino-2-butene-1,4-diones.Translated from Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 480–482, February, 1996 相似文献
19.
The first evidence that α-acylnitrone is an intermediate in the base-promoted reaction of 4-nitro-N,N-diethylaniline with aceptophenome to give an enaminoketone was obtained.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1645–1647, August, 1998. 相似文献
20.