全文获取类型
收费全文 | 377篇 |
免费 | 6篇 |
专业分类
化学 | 290篇 |
晶体学 | 2篇 |
力学 | 21篇 |
数学 | 15篇 |
物理学 | 55篇 |
出版年
2020年 | 3篇 |
2019年 | 6篇 |
2017年 | 3篇 |
2016年 | 3篇 |
2014年 | 4篇 |
2013年 | 5篇 |
2012年 | 17篇 |
2011年 | 21篇 |
2010年 | 11篇 |
2009年 | 8篇 |
2008年 | 19篇 |
2007年 | 33篇 |
2006年 | 13篇 |
2005年 | 23篇 |
2004年 | 16篇 |
2003年 | 19篇 |
2002年 | 16篇 |
2001年 | 17篇 |
2000年 | 13篇 |
1999年 | 6篇 |
1998年 | 7篇 |
1997年 | 7篇 |
1996年 | 7篇 |
1995年 | 6篇 |
1994年 | 8篇 |
1993年 | 2篇 |
1992年 | 3篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 3篇 |
1987年 | 3篇 |
1986年 | 5篇 |
1985年 | 4篇 |
1984年 | 7篇 |
1983年 | 2篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 2篇 |
1978年 | 4篇 |
1977年 | 3篇 |
1976年 | 2篇 |
1975年 | 4篇 |
1974年 | 4篇 |
1973年 | 8篇 |
1972年 | 3篇 |
1971年 | 2篇 |
1970年 | 2篇 |
1969年 | 3篇 |
1968年 | 2篇 |
排序方式: 共有383条查询结果,搜索用时 15 毫秒
1.
Masaki Kurokiba Naoto TanakaAtusi Tani 《Journal of Mathematical Analysis and Applications》2002,272(2):448-457
In this paper we consider the Eguchi-Oki-Matsumura equation which consists of the fourth- and second-order coupled equations of parabolic type. It is shown that this system admits the unique global solution. 相似文献
2.
Mechanism for polymerization of ε-caprolactam in the presence of both sodium and aluminum caprolactamate was investigated at 171°C. The role of Al(Cap)3 as an initiator was revealed. The apparent rate constant of propagation reaction decreased with the increase in the concentration of Al(Cap)3, as the two different metal salts interact even at 171°C. The activation energy of the overall polymerization reaction with this catalyst system was estimated to be 41.18 kcal/mole. 相似文献
3.
Summary A porous polymer resin loaded with hydrous zirconium oxide (Zr-gel) was evaluated as a stationary phase for the liquid chromatographic separation of disubstituted aromatic compounds. The prepared Zr-gel was used to separate disubstituted phenols andortho-substituted benzoic acid derivatives in reversed-phase mode. The retention time of catechol was greater than those of other disubstituted phenols; this implies that the Zr-gel has specificity for the phenolic hydroxyl group. The retention behavior ofortho-substituted benzoic acid derivatives on the Zr-gel was also evaluated in reversedphase mode using buffer. Phthalic acid was specifically retained in the vicinity of pH 6.0, which has been regarded as the equal adsorbic point. Similar behavior was also observed for salicylic acid, although the retention time of salicylic acid was less than that of phthalic acid. It seems that the specific retention behavior of hydrous zirconium oxide is a result of complexation with ligands such as hydroxyl and carboxyl groups. The results of this study have revealed that the retention mechanism of hydrous zirconium oxide is a combination of ion exchange and interaction based on complexation with ligands. 相似文献
4.
Kunishima M Kitao A Kawachi C Watanabe Y Iguchi S Hioki K Tani S 《Chemical & pharmaceutical bulletin》2002,50(4):549-550
Racemization of the C-terminal amino acid (Ala) has been studied in various solvents during coupling between 4-methoxybenzyloxycarbonyl (Z(OMe))-Gly-L-Ala-OH and phenylalanine benzyl ester (H-Phe-OBzl) with 4-(4,6-dimethoxy-1,3,5-thiazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). The reaction occurred without substantial racemization in AcOEt, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), CH3CN, and 2-PrOH, while a slight racemization was observed in dimethyl sulfoxide (DMSO), EtOH, and MeOH. The extent of racemization may correlate with the polarity of the solvents. 相似文献
5.
6.
Ammonium aromatic diselenoates were synthesized by reacting aromatic diselenoic acid 2-(trimethylsilyl)ethyl esters derived from aluminum 2-(trimethylsilyl)ethyl selenolate with aromatic selenoic acid O-methyl esters with ammonium fluorides. The results of molecular structure analysis and NMR studies of ammonium salts supported the double-bond character between the carbon atom and selenium atoms. 相似文献
7.
Catalytic activities of the reaction products of diethylzinc or triethylaluminum with primary amines in the polymerization of propylene oxide were studied. Generally, organozinc compounds give higher ratio of the crystalline to the amorphous polymer than the organoaluminums. In the reactions of organometallic compounds with primary amines, Et2AlNPhAlEt2, Et2AlN-t-BuAlEt2, EtZnNH-t-Bu, and EtZn-t-BuZnEt were isolated in crystalline state. EtZnN-t-BuZnEt proved to be an excellent catalyst for the stereospecific polymerization of propylene oxide and forms coordination complexes with some electron donors such as dioxane, pyridine, epichlorohydrin and propylene oxide. The propylene oxide complex is unstable in solution and decomposes at temperatures above room temperature to give poly(propylene oxide), while the pyridine complex has no catalytic activity. Therefore, it is concluded that the polymerization of propylene oxide with this catalyst proceeds through the coordination of propylene oxide to the zinc atom of the catalyst. 相似文献
8.
9.
Shintaro Wakamatsu Yuka Takahashi Dr. Hidetsugu Tabata Dr. Tetsuta Oshitari Norihiko Tani Prof. Dr. Isao Azumaya Dr. Yukiteru Katsumoto Dr. Takeyuki Tanaka Dr. Shinzo Hosoi Prof. Dr. Hideaki Natsugari Prof. Dr. Hideyo Takahashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(22):7056-7063
The stereochemistry around the N‐benzoylated indole moiety of indometacin was studied by restricting the rotation about the N? C7′ and/or C7′? C1′ bond. In the 2′,6′‐disubstituted ones, an atropisomeric property was found and the atropoisomers were separated and isolated as stable forms. Their biological abilities to inhibit cyclooxygenase‐1 (COX‐1) and cyclooxygenase‐2 (COX‐2) were examined. Only the aR‐isomer showed specific inhibition of COX‐1, and COX‐2 was not inhibited by either atropisomer. Conformational analysis in NMR studies and X‐ray crystallography, and CD spectra in combination with calculations were utilized to elucidate the bioactive conformations. 相似文献
10.
Dr. Hiromi Oshita Takashi Suzuki Kyohei Kawashima Prof. Dr. Hitoshi Abe Prof. Dr. Fumito Tani Prof. Dr. Seiji Mori Prof. Dr. Tatsuo Yajima Prof. Dr. Yuichi Shimazaki 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(32):7649-7658
In order to gain new insights into the effect of the π–π stacking interaction of the indole ring with the CuII–phenoxyl radical as seen in the active form of galactose oxidase, we have prepared a CuII complex of a methoxy-substituted salen-type ligand, containing a pendent indole ring on the dinitrogen chelate backbone, and characterized its one-electron-oxidized forms. The X-ray crystal structures of the oxidized CuII complex exhibited the π–π stacking interaction of the indole ring mainly with one of the two phenolate moieties. The phenolate moiety in close contact with the indole moiety showed the characteristic phenoxyl radical structural features, indicating that the indole ring favors the π–π stacking interaction with the phenoxyl radical. The UV/Vis/NIR spectra of the oxidized CuII complex with the pendent indole ring was significantly different from those of the complex without the side-chain indole ring, and the absorption and CD spectra exhibited a solvent dependence, which is in line with the phenoxyl radical–indole stacking interaction in solution. The other physicochemical results and theoretical calculations strongly support that the indole ring, as an electron donor, stabilizes the phenoxyl radical by the π–π stacking interaction. 相似文献