全文获取类型
收费全文 | 906篇 |
免费 | 13篇 |
国内免费 | 5篇 |
专业分类
化学 | 708篇 |
晶体学 | 7篇 |
力学 | 11篇 |
数学 | 46篇 |
物理学 | 152篇 |
出版年
2021年 | 4篇 |
2019年 | 6篇 |
2018年 | 4篇 |
2017年 | 4篇 |
2016年 | 7篇 |
2015年 | 13篇 |
2014年 | 9篇 |
2013年 | 54篇 |
2012年 | 43篇 |
2011年 | 40篇 |
2010年 | 26篇 |
2009年 | 28篇 |
2008年 | 43篇 |
2007年 | 39篇 |
2006年 | 40篇 |
2005年 | 45篇 |
2004年 | 53篇 |
2003年 | 38篇 |
2002年 | 37篇 |
2001年 | 18篇 |
2000年 | 13篇 |
1999年 | 12篇 |
1998年 | 10篇 |
1997年 | 11篇 |
1996年 | 12篇 |
1995年 | 12篇 |
1994年 | 7篇 |
1993年 | 4篇 |
1992年 | 15篇 |
1991年 | 10篇 |
1990年 | 8篇 |
1989年 | 12篇 |
1988年 | 8篇 |
1987年 | 7篇 |
1986年 | 6篇 |
1985年 | 23篇 |
1984年 | 16篇 |
1983年 | 11篇 |
1982年 | 16篇 |
1981年 | 19篇 |
1980年 | 17篇 |
1979年 | 21篇 |
1978年 | 8篇 |
1977年 | 17篇 |
1976年 | 11篇 |
1975年 | 12篇 |
1974年 | 10篇 |
1973年 | 10篇 |
1967年 | 4篇 |
1930年 | 4篇 |
排序方式: 共有924条查询结果,搜索用时 31 毫秒
911.
Yuji Hanzawa Nobuhito Tabuchi Kosuke Saito Satoshi Noguchi Takeo Taguchi 《Angewandte Chemie (International ed. in English)》1999,38(16):2395-2398
The chiral monodentate phosphane ligand ( R )-MOP facilitated the first enantioselective nucleophilic 1,2-addition of an “unmasked” acyl anion to a carbonyl group in the PdII-catalyzed reaction of α,β-unsaturated ketones with acylzirconocene chlorides [Eq. (1), 66 % ee, 88 % yield; (R)-MOP=(R)-2-(diphenylphosphanyl)-2′-methoxy-1,1′-binaphthyl]. 相似文献
912.
913.
914.
Masatoshi Miyamoto Keigo Aoi Takeo Saegusa 《Journal of polymer science. Part A, Polymer chemistry》1997,35(5):933-945
The cationic ring-opening polymerization of six-membered cyclic pseudoureas, 2-(1-pyrrolidinyl)- ( 2a ) and 2-morpholino-5,6-dihydro-4H-1,3-oxazine ( 2b ), was examined, which proceeded in two different ways, depending on the nature of initiator. The polymerization of 2 with methyl p-toluenesulfonate or trifluoromethanesulfonate (MeOTf) produced poly[(N-carbamoylimino)trimethylene], while that with benzyl chloride or bromide or methyl iodide gave a polymer consisting of 1,3-diazin-2-one-1,3-diylalkylene unit (the main component) and (N-carbamoylimino)trimethylene unit. The cationic ring-opening polymerization of seven-membered cyclic pseudourea, 2-(1-pyrrolidinyl)-4,5,6,7-tetrahydro-4H-1,3-oxazepine ( 3 ) was also examined. The polymerization of 3 with MeOTf as initiator gave poly{[N-(1-pyrrolidinycarbonyl)imino]tetra-methylene}. With benzyl chloride, on the other hand, no polymerization of 3 proceeded but, instead, the quantitative isomerization of 3 to 1,1′-carbonyldipyrrolidine took place. The polymerization mechanism of 2 and 3 as well as the isomerization mechanism of 3 were discussed with comparing them to the polymerization mechanism of five-membered pseudoureas. © 1977 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 933–945, 1997 相似文献
915.
Takeo Yamaguchi Shin-Ichi Nakao Shoji Kimura 《Journal of Polymer Science.Polymer Physics》1997,35(3):469-477
A model that can express the swelling of the filling-type membrane was developed by modifying a model that was developed for a crystalline polymer. The filling-type membrane is composed of two different polymers. One is porous substrate and another is a polymer that filled pores of the substrate. The filling technique can effectively suppress polymer swelling due to the substrate matrix. The model needs two parameters: one is a unit ratio of tie segments in the substrate to the filling polymer, f, which can express a mechanical strength of the substrate, and another is the Flory interaction parameter, χ, between the filling polymer and a solvent that expresses a mixing energy. A porous high-density polyethylene film was used as a porous substrate, and plasma-graft filling polymerization technique could make the filling-type membrane. Methylacrylate was used as a grafting monomer that filled the pores of substrate. A swelling behavior of the filling-type membrane and pure poly(methylacrylate) were measured by the vapor sorption method at different solvent activities. The model was in good agreement with experimental results for the filling-type membrane. Using the model, swelling of the filling-type polymer was compared with a crosslinked polymer, which can be expressed by Flory and Rehner model. The comparison showed that the filling technique is a good way to suppress polymer swelling, and a high crosslinking density is needed to obtain the same level of swelling suppression effect the filling type membrane showed. © 1997 John Wiley & Sons, Inc. 相似文献
916.
Takeo Shimidzu 《Macromolecular Symposia》1996,104(1):127-135
Approaches to polymer superlattice and molecular devices are shown, demonstrating with functional molecule material by incorporation of a functional molecule into the conducting polymer, conjugating copolymer superlattice by a novel potential programmed electro polymerization, ultrahigh anisotropic conductive LB heterolayers, and porphyrin arrays connected with conducting molecular wire and insulating molecular wire. These results show a practical method to fabricate ultimate functional materials such as molecular device which is the smallest functional material, and quantum functional material which creates a novel nature. 相似文献
917.
Bulk radical polymerization of styrene in the presence of nitronyl nitroxides (2-(4-substituted phenyl)-4,4,5,5-tetramethyl-4,5-dihydroimidazolyl-1-oxyl 3-oxide) was studied. All nitronyl nitroxides, like other nitroxyl radicals such as 2,2,6,6-tetramethylpiperidine 1-oxyl radical (TEMPO), act as reversible radical scavengers. The efficiency of controlling the polymerization is affected by the substituent at the 4′-position. The efficiency increases with electron donating strength of 4′-substituents, at least at the beginning of the reaction. However, the thermal stability of nitronyl nitroxides decreases in the same order. Thus, TEMPO is more suitable than nitronyl nitroxides for controlled/“living” radical polymerization of styrene. 相似文献
918.
919.
Koki Fujimura Dr. Yoshihiro Ueda Dr. Yousuke Yamaoka Prof. Kiyosei Takasu Prof. Takeo Kawabata 《Angewandte Chemie (International ed. in English)》2023,62(30):e202303078
A method for rotaxane synthesis by enlargement of the size of the terminal phenol group of the axle component by aromatic bromination has been developed. This method may be regarded as an end-capping strategy involving the swelling of the phenol group at the axle terminal. The advantages of the present strategy include: ready availability of axle components with a variety of swelling precursors, wide product scope (19 examples given including a [3]rotaxane), mild conditions for the swelling process, rich potential for the derivatization of the brominated rotaxanes, and possible release of the axle component by degradative dethreading of the thermally stable brominated rotaxanes under the basic conditions. 相似文献
920.