全文获取类型
收费全文 | 497篇 |
免费 | 12篇 |
专业分类
化学 | 395篇 |
晶体学 | 13篇 |
力学 | 5篇 |
数学 | 16篇 |
物理学 | 80篇 |
出版年
2023年 | 1篇 |
2022年 | 3篇 |
2021年 | 6篇 |
2019年 | 10篇 |
2018年 | 3篇 |
2017年 | 5篇 |
2016年 | 6篇 |
2015年 | 7篇 |
2014年 | 7篇 |
2013年 | 27篇 |
2012年 | 18篇 |
2011年 | 37篇 |
2010年 | 18篇 |
2009年 | 16篇 |
2008年 | 37篇 |
2007年 | 36篇 |
2006年 | 35篇 |
2005年 | 32篇 |
2004年 | 21篇 |
2003年 | 22篇 |
2002年 | 16篇 |
2001年 | 14篇 |
2000年 | 9篇 |
1999年 | 2篇 |
1998年 | 4篇 |
1997年 | 7篇 |
1996年 | 7篇 |
1994年 | 3篇 |
1993年 | 6篇 |
1992年 | 8篇 |
1991年 | 3篇 |
1990年 | 5篇 |
1989年 | 5篇 |
1988年 | 5篇 |
1987年 | 6篇 |
1986年 | 3篇 |
1985年 | 5篇 |
1984年 | 6篇 |
1983年 | 6篇 |
1982年 | 4篇 |
1981年 | 2篇 |
1980年 | 3篇 |
1979年 | 7篇 |
1978年 | 8篇 |
1977年 | 3篇 |
1976年 | 8篇 |
1975年 | 3篇 |
1974年 | 2篇 |
1973年 | 2篇 |
排序方式: 共有509条查询结果,搜索用时 15 毫秒
31.
Preconcentration by collection of metal complexes on chitin has been applied to the spectrophotometric determination of iron in water. The iron is collected as its 1,10-phenanthroline (phen) complex on a column of chitin in the presence of tetraphenylborate as counter-ion. The iron(II)-phen complex retained on the chitin is eluted with an acetone-1M acetic acid mixture (8:2 v/v), and the absorbance of the eluate is measured at 512 nm. Beer's law is obeyed over the concentration range 1.1-11.2 mug of iron in 10 ml of eluate. In the presence of EDTA as masking agent, Ca, Mg, Al, Mn, Zn, Cd and Pb do not interfere in concentrations up to 100 times that of iron(II) and Co, Ni and Cu do not interfere in concentrations up to 20 times that of iron(II). Common inorganic anions do not interfere in concentrations up to 10,000 times that of iron(II). The proposed method has been applied to determination of iron in tap water. 相似文献
32.
A nickel-catalyzed cycloaddition has been developed where readily available anthranilic acid derivatives react with alkynes to afford substituted indoles. The reaction involves oxidative addition of Ni(0) to an ester moiety, which allows intermolecular addition to alkynes via decarbonylation and 1,3-acyl migration. 相似文献
33.
In the presence of a palladium catalyst, treatment of γ-acyloxy-α,β-unsaturated ketone with bis(iodozincio)methane caused umpolung of π-allylpalladium to give a zinc dienolate. Thus formed zinc species afforded a cyclohexene derivative via a self-condensation reaction. It is noteworthy that the three adjacent stereogenic centers were created in a single process with quite high diastereoselectivity. 相似文献
34.
Horie H Koyama I Kurahashi T Matsubara S 《Chemical communications (Cambridge, England)》2011,47(9):2658-2660
The linear codimerization of acrylates and alkynes to produce 1,3-dienes is successfully demonstrated using a nickel catalyst in association with 2-aminopyridine as an additive. 相似文献
35.
Enones were found to react with allenes intermolecularly in the presence of a catalytic amount of a nickel-iminophosphine complex to provide dihydropyrans via oxidative cyclization of an enone and Ni(0). 相似文献
36.
Li HH Imai Y Yamanaka M Hayami Y Takiue T Matsubara H Aratono M 《Journal of colloid and interface science》2011,359(1):189-193
To investigate the counterion effects, we employed dodecyltrimethylammonium bromide (DTABr)-dodecyltrimethylammonium tetrafluoroborate (DTABF(4)) mixed aqueous solutions and measured their surface tensions, then analyzed these data in a thermodynamic treatment. The tensiometry showed that DTABF(4) was more effective in lowering the surface tension of water. The phase diagram of adsorption demonstrated that the surface was enriched with BF(4)(-) ions, but the composition of Br(-) ions in the adsorbed film was slightly enhanced compared to the ideal mixing criteria. These were explained in terms of the size and polarizability of counterions. Moreover, the distribution of counterions of the DTABr-DTABF(4) mixtures in the adsorbed film is greatly different from that of the 1-hexyl-3-methylimidazolium bromide (HMIMBr)-1-hexyl-3-methylimidazolium tetrafluoroborate (HMIMBF(4)) mixtures, where a stronger hydrogen-bonding exists between BF(4)(-) and HMIM(+) ions. These findings suggest that the adsorption of counterions in electric double layers is likely subject to two factors: the nature of counterion and their interactions with surfactant ions. 相似文献
37.
Noriaki Nishiguchi Takafumi Kinuta Yoko Nakano Dr. Takunori Harada Dr. Nobuo Tajima Tomohiro Sato Prof. Dr. Michiya Fujiki Prof. Dr. Reiko Kuroda Prof. Dr. Yoshio Matsubara Dr. Yoshitane Imai 《化学:亚洲杂志》2011,6(4):1092-1098
The solid‐state chiral optical properties of a 4‐(2‐arylethynyl)‐benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the arylethynyl group of the achiral 4‐(2‐arylethynyl)‐benzoic acid component molecule rather than the chirality of the amine component molecule. 相似文献
38.
The decarbonylative cycloadditions of phthalic anhydrides with allenes were performed by using nickel catalyst. The asymmetric variant of the cycloaddition was also achieved by using chiral phosphine ligands to provide δ-lactones enantioselectively. 相似文献
39.
Matsubara H Ohtomi E Aratono M Bain CD 《The journal of physical chemistry. B》2008,112(37):11664-11668
Wetting of water by hexadecane has been investigated by ellipsometry as a function of the concentration of the cationic surfactant dodecyltrimethylammonium bromide (DTAB) in the aqueous phase and temperature. Three phases are identified: a 2-D gas of hexadecane molecules and DTAB molecules, a 2-D liquid comprising a mixed monolayer of hexadecane and DTAB, and a 2-D 'solid' phase. Evidence is presented to support the hypothesis that the liquid-solid phase transition is actually a wetting transition in which a surface-frozen layer of pure hexadecane wets the liquid-like mixed monolayer of hexadecane and DTAB. The triple point, at which the three phases coexist, is located at a temperature of 17.3 degrees C and DTAB concentration of 0.75 mmol kg (-1). The slopes of the three phase boundaries are analyzed thermodynamically. 相似文献
40.
Yoshitane Imai Dr. Katuzo Murata Kakuhiro Kawaguchi Tomohiro Sato Nobuo Tajima Dr. Reiko Kuroda Dr. Yoshio Matsubara Dr. 《化学:亚洲杂志》2008,3(3):625-629
A solid‐state fluorescent host system was created by self‐assembly of a 21‐helical columnar organic fluorophore composed of (1R,2S)‐2‐amino‐1,2‐diphenylethanol and fluorescent 1‐pyrenecarboxylic acid. This host system has a characteristic 21‐helical columnar hydrogen‐ and ionic‐bonded network. Channel‐like cavities are formed by self‐assembly of this column, and various guest molecules can be included by tuning the packing of this column. Moreover, the solid‐state fluorescence of this host system can change according to the included guest molecules. This occurs because of the change in the relative arrangement of the pyrene rings as they adjust to the tuning of the packing of the shared 21‐helical column, according to the size of the included guest molecules. Therefore, this host system can recognize slight differences in molecular size and shape. 相似文献