全文获取类型
收费全文 | 6291篇 |
免费 | 574篇 |
国内免费 | 596篇 |
专业分类
化学 | 3832篇 |
晶体学 | 36篇 |
力学 | 208篇 |
综合类 | 73篇 |
数学 | 2194篇 |
物理学 | 1118篇 |
出版年
2024年 | 8篇 |
2023年 | 44篇 |
2022年 | 64篇 |
2021年 | 93篇 |
2020年 | 157篇 |
2019年 | 162篇 |
2018年 | 164篇 |
2017年 | 215篇 |
2016年 | 181篇 |
2015年 | 199篇 |
2014年 | 279篇 |
2013年 | 966篇 |
2012年 | 266篇 |
2011年 | 297篇 |
2010年 | 255篇 |
2009年 | 317篇 |
2008年 | 336篇 |
2007年 | 353篇 |
2006年 | 344篇 |
2005年 | 289篇 |
2004年 | 274篇 |
2003年 | 252篇 |
2002年 | 850篇 |
2001年 | 175篇 |
2000年 | 184篇 |
1999年 | 116篇 |
1998年 | 140篇 |
1997年 | 77篇 |
1996年 | 87篇 |
1995年 | 74篇 |
1994年 | 58篇 |
1993年 | 36篇 |
1992年 | 28篇 |
1991年 | 16篇 |
1990年 | 17篇 |
1989年 | 15篇 |
1988年 | 16篇 |
1987年 | 12篇 |
1986年 | 7篇 |
1985年 | 4篇 |
1984年 | 9篇 |
1982年 | 3篇 |
1981年 | 3篇 |
1980年 | 2篇 |
1979年 | 5篇 |
1978年 | 3篇 |
1974年 | 1篇 |
1973年 | 2篇 |
1968年 | 1篇 |
1936年 | 1篇 |
排序方式: 共有7461条查询结果,搜索用时 15 毫秒
11.
Z. J. Yu L. J. Liu R. X. Zhuo 《Journal of polymer science. Part A, Polymer chemistry》2003,41(1):13-21
The ring‐opening polymerization of ε‐caprolactone (ε‐CL), initiated by carboxylic acids such as benzoic acid and chlorinated acetic acids under microwave irradiation, was investigated; with this method, no metal catalyst was necessary. The product was characterized as poly(ε‐caprolactone) (PCL) by 1H NMR spectroscopy, Fourier transform infrared spectroscopy, ultraviolet spectroscopy, and gel permeation chromatography. The polymerization was significantly improved under microwave irradiation. The weight‐average molecular weight (Mw) of PCL reached 44,800 g/mol, with a polydispersity index [weight‐average molecular weight/number‐average molecular weight (Mw/Mn)] of 1.6, when a mixture of ε‐CL and benzoic acid (25/1 molar ratio) was irradiated at 680 W for 240 min, whereas PCL with Mw = 12,100 and Mw/Mn = 4.2 was obtained from the same mixture by a conventional heating method at 210 °C for 240 min. A degradation of the resultant PCL was observed during microwave polymerization with chlorinated acetic acids as initiators, and this induced a decrease in Mw of PCL. However, the degradation was hindered by benzoic acid at low concentrations. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 13–21, 2003 相似文献
13.
14.
Ke Sha Dongshuang Li Yapeng Li Xiaotian Liu Shuwei Wang Jingqi Guan Jingyuan Wang 《Journal of polymer science. Part A, Polymer chemistry》2007,45(22):5037-5049
Amphiphilic diblock copolymer polycaprolactone‐block‐poly(glycidyl methacrylate) (PCL‐b‐PGMA) was synthesized via enzymatic ring‐opening polymerization (eROP) and atom transfer radical polymerization (ATRP). Methanol first initiated eROP of ?‐caprolactone (?‐CL) in the presence of biocatalyst Novozyme‐435 under anhydrous conditions. The resulting monohydroxyl‐terminated polycaprolactone (PCL–OH) was subsequently converted to a bromine‐ended macroinitiator (PCL–Br) for ATRP by esterification with α‐bromopropionyl bromide. PCL‐b‐PGMA diblock copolymers were synthesized in a subsequent ATRP of glycidyl methacrylate (GMA). A kinetic analysis of ATRP indicated a living/controlled radical process. The macromolecular structures were characterized for PCL–OH, PCL–Br, and the block copolymers by means of nuclear magnetic resonance, gel permeation chromatography, and infrared spectroscopy. Differential scanning calorimetry and wide‐angle X‐ray diffraction analyses indicated that the copolymer composition (?‐CL/GMA) had a great influence on the thermal properties. The well‐defined, amphiphilic diblock copolymer PCL‐b‐PGMA self‐assembled into nanoscale micelles in aqueous solutions, as investigated by dynamic light scattering and transmission electron microscopy. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5037–5049, 2007 相似文献
15.
Yozo Miura Hiroyuki Dote Hiroyuki Kubonishi Kenichi Fukuda Tomoko Saka 《Journal of polymer science. Part A, Polymer chemistry》2007,45(6):1159-1169
A dendritic macroinitiator having 16 TEMPO‐based alkoxyamines, Star‐16 , was prepared by the reaction of a dendritic macroinitiator having eight TEMPO‐based alkoxyamines, [G‐3]‐OH , with 4,4′‐bis(chlorocarbonyl)biphenyl. The nitroxide‐mediated radical polymerization (NMRP) of styrene (St) from Star‐16 gave 16‐arm star polymers with PDI of 1.19–1.47, and NMPR of 4‐vinylpyridine from the 16‐arm star polymer gave 16‐arm star diblock copolymers with PDI of 1.30–1.43. The ring‐opening polymerization of ε‐caprolactone from [G‐3]‐OH and the subsequent NMRP of St gave AB8 9‐miktoarm star copolymers with PDI of 1.30–1.38. The benzyl ether linkages of the 16‐arm star polymers and the AB8 9‐miktoarm star copolymers were cleaved by treating with Me3SiI, and the resultant poly(St) arms were investigated by size exclusion chromatography (SEC). The SEC results showed PDIs of 1.23–1.28 and 1.18–1.22 for the star polymers and miktoarm stars copolymers, respectively, showing that they have well‐controlled poly(St) arms. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1159–1169, 2007. 相似文献
16.
Hisatoyo Morinaga Bungo Ochiai Hideharu Mori Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2007,45(5):736-744
Natural human hair was successfully modified by the graft polymerization of trimethylene carbonate, β‐propiolactone, ε‐caprolactone, glycidol, ε‐caprolactam, and 5,5‐dimethyl‐1,3‐dioxane‐2‐thione. In contrast, we could not modify natural human hair by the graft polymerization of oxetane under similar conditions. The model reaction suggested that the main initiating species in these polymerizations were the amino, thiol, and hydroxyl groups in hair, which could induce ring‐opening polymerization. Among the tested monomers, β‐propiolactone was most effective for hair modification with its graft polymer, whose concentration was as high as 0.5 g/g of hair though polymerization under mild conditions. The effects of the hair pretreatment and polymerization temperature on the weight ratio of the grafted polymers were also investigated. Hair modified by grafted polymers was characterized with scanning electron microscopy and Fourier transform infrared measurements. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 736–744, 2007 相似文献
17.
为改进Fuzzy HX环的结果,使之包含Fuzzy商环,提出了弱Fuzzy HX环的概念,研究了它的性质与结构,并重新讨论了拟Fuzzy商环,证明了在正则条件下拟Fuzzy商环与弱Fuzzy HX环的统一性:同时也得到了一致弱Fuzzy HX环与普通Fuzzy商环的关系。 相似文献
18.
19.
环上矩阵的广义Moore-Penrose逆 总被引:14,自引:0,他引:14
本文给出带有对合的有1的结合环上一类矩阵的广义Moore-Penrose逆存在的充要条件,而这类矩阵概括了左右主理想整环,单Artin环上所有矩阵。 相似文献
20.
本文讨论临界可压缩模类和结合环的弱Jacobson根.首先,我们证明了非平凡的临界可压缩模类是素模的特殊类.其次,我们引入结合环的弱Jacobson根.弱Jaonbson根是特殊根.最后,我们给出有关弱本原环,半弱本原环和弱Jacobson根环的某些性质. 相似文献