全文获取类型
收费全文 | 1370篇 |
免费 | 70篇 |
国内免费 | 6篇 |
专业分类
化学 | 1181篇 |
晶体学 | 15篇 |
力学 | 13篇 |
数学 | 57篇 |
物理学 | 180篇 |
出版年
2023年 | 11篇 |
2022年 | 20篇 |
2021年 | 18篇 |
2020年 | 30篇 |
2019年 | 43篇 |
2018年 | 19篇 |
2017年 | 18篇 |
2016年 | 51篇 |
2015年 | 43篇 |
2014年 | 44篇 |
2013年 | 81篇 |
2012年 | 107篇 |
2011年 | 108篇 |
2010年 | 74篇 |
2009年 | 61篇 |
2008年 | 102篇 |
2007年 | 86篇 |
2006年 | 87篇 |
2005年 | 79篇 |
2004年 | 80篇 |
2003年 | 54篇 |
2002年 | 39篇 |
2001年 | 16篇 |
2000年 | 14篇 |
1999年 | 11篇 |
1998年 | 6篇 |
1997年 | 9篇 |
1996年 | 12篇 |
1995年 | 9篇 |
1994年 | 8篇 |
1993年 | 12篇 |
1992年 | 6篇 |
1991年 | 8篇 |
1990年 | 10篇 |
1989年 | 7篇 |
1988年 | 4篇 |
1987年 | 5篇 |
1986年 | 2篇 |
1985年 | 8篇 |
1984年 | 8篇 |
1983年 | 3篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1980年 | 7篇 |
1979年 | 4篇 |
1978年 | 2篇 |
1977年 | 5篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1937年 | 1篇 |
排序方式: 共有1446条查询结果,搜索用时 0 毫秒
61.
[reaction: see text] The Pt-catalyzed carboselenation of terminal alkynes with selenoesters provided vinylselenides regio- and stereoselectively in moderate yields. 相似文献
62.
63.
Daigo Hayashi Dr. Tomohiro Tsuda Prof. Dr. Ryo Shintani 《Angewandte Chemie (International ed. in English)》2023,62(50):e202313171
A palladium-catalyzed skeletal rearrangement of 2-(2-allylarylsilyl)aryl triflates has been developed to give highly fused tetrahydrophenanthrosilole derivatives via unprecedented 1,5-C−Pd/C−Si bond exchange. The reaction pathways can be switched toward 4-membered ring-forming C(sp2)−H alkylation by tuning the reaction conditions to give completely different products, fused dihydrodibenzosilepin derivatives, from the same starting materials. The inspection of the reaction conditions revealed the importance of carboxylates in promoting the C−Pd/C−Si bond exchange. 相似文献
64.
65.
Takahiro Matsumoto Seikou Nakamura Naoto Kojima Tomohiro Hasei Masayuki Yamashita Tetsushi Watanabe Hisashi Matsuda 《Tetrahedron letters》2017,58(36):3574-3578
From the methanolic extract of the aerial parts of Isodon japonicus, two new ent-kaurane diterpenes, isodonterpenes I and II, were isolated together with 10 known diterpenes. Their chemical structures were elucidated on the basis of chemical and physicochemical evidence. The absolute configuration of isodonterpene I was elucidated by Cu-Kα X-ray crystallographic analysis. Antimutagenic activities of the major diterpenes were evaluated by the Ames test. This study represents the first evaluation of the antimutagenic activities of ent-kaurane diterpenes. 相似文献
66.
Surasak Seesukphronrarak Shinichi Kawasaki Shigeki Kuwata Toshikazu Takata 《Journal of polymer science. Part A, Polymer chemistry》2019,57(24):2602-2605
Two novel 9,9‐difunctionalized fluorene‐type monomers, 9,9‐bis(4‐hydroxyphenyl‐ and 4‐aminophenyl)‐2,3:6,7‐dibenzofluorenes, are synthesized by the reaction of dibenzenzofluorenone with phenol and aniline. These monomers are used for the preparation of polyester and polyimide as the typical polymers to evaluate the property change such as thermal stability caused by the benzene rings fused to the fluorene skeleton with keeping good solubility, in comparison with the polymers derived from simple fluorenone. In fact, these two new polymers have the fairly enhanced thermal stability and refractive index value along with satisfactory solubility in organic solvents, enough to emphasize the fusion effect. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2602–2605 相似文献
67.
Prof. Dr. Yasuchika Hasegawa Takafumi Matsui Dr. Yuichi Kitagawa Dr. Takayuki Nakanishi Dr. Tomohiro Seki Prof. Dr. Hajime Ito Prof. Dr. Yuta Nakasaka Prof. Dr. Takao Masuda Prof. Dr. Koji Fushimi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(53):12308-12315
Oxygen-sensitive and near-infrared (NIR) luminescent YbIII coordination polymers incorporating ligands based on pyrene derivatives were synthesized: YbIII–TBAPy and YbIII–TIAPy (TBAPy: 1,3,6,8-tetrakis(p-benzoate)pyrene; TIAPy: 1,3,6,8-tetrakis(3,5-isophthalic acid)pyrene). The coordination structures of these materials have been characterized by means of electrospray ionization mass spectrometry, X-ray diffraction analysis, and thermogravimetric analysis. Moreover, the porous structure of YbIII–TIAPy has been evaluated by measuring its N2 adsorption isotherm. The NIR luminescence properties of YbIII–TBAPy and YbIII–TIAPy have been examined by acquiring emission spectra and determining emission lifetimes under air or argon and in vacuo. YbIII–TIAPy exhibited high thermal stability (with a decomposition temperature of 400 °C), intense luminescence (with an emission quantum yield under argon of 6.6 %), and effective oxygen-sensing characteristics. These results suggest that NIR luminescent YbIII coordination polymers prepared using pyrene derivatives could have applications in novel thermo-stable oxygen sensors. 相似文献
68.
Eguchi S Suzuki T Okawa T Matsushita Y Yashima E Okamoto Y 《The Journal of organic chemistry》1996,61(21):7316-7319
Both optical isomers of a quinazoline alkaloid, vasicinone, were synthesized by two different methods. The first method used (3S)-3-hydroxy-gamma-lactam as a chiral synthon, which was, after O-TBDMS protection, o-azidobenzoylated followed by treatment with tri-n-butylphosphine to afford (S)-(-)-vasicinone via the tandem Staudinger/intramolecualr aza-Wittig reaction. The second method utilized asymmetric oxygenation of deoxyvasicinone with (1S)-(+)- or (1R)-(-)-(10-camphorsulfonyl)oxaziridine (the Davis reagent), respectively. The aza-enolate anion of deoxyvasicinone was treated with (S)-(+)-reagent to afford (R)-(+)-vasicinone in 71% ee, while the reaction with (R)-(-)-reagent gave (S)-(-)-vasicinone in 62% ee. The optical purity was analyzed by HPLC on specially modified cellulose as a stationary phase. These results provided a facile method to prepare both optical isomers of vasicinone and confirmed the recently reversed stereochemistry of natural (-)-vasicinone. 相似文献
69.
This paper describes characterization of molecular orientation for azobenzene moieties in a polymer nanosheet. Copolymers of N-[4-(phenylazo)phenyl] acrylamide (PAZoA) with tert-pentyl acrylamide (tPA) were synthesized and the monolayers deposited on tapered quartz waveguides by Langmuir–Blodgett (LB) technique. Spectroscopic properties of the copolymer (p(tPA/PAZoA)) monolayers were monitored by integrated optical waveguide technique on the molecular level. Molecular orientation of the azobenzene was precisely determined by polarized absorption spectra. It was found that the azobenzene groups took a horizontal orientation and distributed uniformly in the p(tPA/PAZoA) monolayer without significant PAZoA aggregation. Photoisomerization process from trans to cis form was also investigated. More than half of the trans form (60–70%) was photoisomerized under unpolarized light irradiation, and the photoisomerization rate was independent on the PAZoA contents. This implies that the microenvironment of PAZoA moieties was almost the same in three different p(tPA/PAZoA) monolayers. 相似文献