全文获取类型
收费全文 | 2816篇 |
免费 | 129篇 |
国内免费 | 10篇 |
专业分类
化学 | 2326篇 |
晶体学 | 12篇 |
力学 | 25篇 |
数学 | 285篇 |
物理学 | 307篇 |
出版年
2023年 | 21篇 |
2022年 | 36篇 |
2021年 | 34篇 |
2020年 | 51篇 |
2019年 | 39篇 |
2018年 | 28篇 |
2017年 | 22篇 |
2016年 | 101篇 |
2015年 | 103篇 |
2014年 | 89篇 |
2013年 | 140篇 |
2012年 | 209篇 |
2011年 | 238篇 |
2010年 | 144篇 |
2009年 | 86篇 |
2008年 | 186篇 |
2007年 | 177篇 |
2006年 | 160篇 |
2005年 | 170篇 |
2004年 | 166篇 |
2003年 | 129篇 |
2002年 | 114篇 |
2001年 | 70篇 |
2000年 | 40篇 |
1999年 | 34篇 |
1998年 | 27篇 |
1997年 | 32篇 |
1996年 | 32篇 |
1995年 | 29篇 |
1994年 | 19篇 |
1993年 | 20篇 |
1992年 | 22篇 |
1991年 | 12篇 |
1990年 | 14篇 |
1989年 | 10篇 |
1988年 | 23篇 |
1987年 | 16篇 |
1986年 | 7篇 |
1985年 | 14篇 |
1984年 | 18篇 |
1983年 | 5篇 |
1982年 | 7篇 |
1981年 | 13篇 |
1980年 | 4篇 |
1979年 | 4篇 |
1978年 | 13篇 |
1977年 | 4篇 |
1976年 | 4篇 |
1975年 | 3篇 |
1969年 | 5篇 |
排序方式: 共有2955条查询结果,搜索用时 15 毫秒
121.
122.
Abstract Organic-inorganic composites (OICs) were prepared via the in-situ polymerization of an organically (phenyl) substituted trialkoxysilane, phenyltriethoxysilane (PhTEOS), in the presence of poly(vinyl acetate) (PVAc). The mechanical reinforcement above T g previously observed in OICs of unfunctionalized organic polymers such as PVAc with acid catalyzed in-situ polymerized tetraalkoxysilane was not observed when the tetraalkoxysilane was replaced with PhTEOS. Although both systems are optically transparent and both exhibit a high degree of hydrogen bonding between the carbonyl of PVAc and the residual hydroxyls of the silicate, the polymerization of the alkoxide is different. The tetra-functional alkoxide polymerizes to form a load-supporting silicate network, leading to a high plateau in the tensile modulus above T g, whereas the trifunctional alkoxide reacts to form primarily low molecular weight oligomers. These increase the T g of the PVAc but do not provide mechanical reinforcement. 相似文献
123.
124.
125.
Thomas Courant Valrie Gaëlle Roullin Cyril Cadiou Maït Callewaert Marie Christine Andry Christophe Portefaix Christine Hoeffel Marie Christine deGoltstein Marc Port Sophie Laurent Luce Vander Elst Robert Muller Michaël Molinari Franoise Chuburu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2012,124(36):9253-9256
126.
Georgy M. Pavlov Anke Teichler Stephanie Höppener Christine Weber Jürgen Nowotny Lars Blankenburg Jürgen Popp Martin D. Hager Benjamin Dietzek Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2012,50(15):3192-3205
In order to form suitable systems designed for resonance energy transfer, a series of monodisperse methacrylate‐based monomers containing rigid π‐conjugated oligo(phenylene ethynylenes) with different sizes of the conjugated systems ( M1 – M3 ), and therefore different optoelectronic properties, were synthesized and subsequently polymerized using the reversible addition–fragmentation chain transfer polymerization technique ( P1 – P3 ). In addition, these oligomers were also copolymerized with methyl methacrylate. The obtained polymers were characterized by 1H NMR spectroscopy, size exclusion chromatography, and analytical ultracentrifugation. The photophysical properties of the polymers were studied by UV–vis absorption and emission spectroscopy in diluted solutions as well as in thin films and compared to the photophysics of the corresponding monomers. Thereby, changes going from monomeric to polymeric systems could be detected in fluorescence quantum yields and lifetimes pointing to energy trapping, e.g., energy transfer. Donor–acceptor copolymers containing different numbers of monomeric units within the side chain exhibit differences in the emission spectra, indicating that energy trapping in polymers is very sensitive to structural properties such as the chain length. UV–vis absorption spectroscopy as well as time‐resolved lifetime studies indicate intrapolymer and interpolymer energy transfer. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
127.
We have carried out zeta-potential measurements on two different OTS (octadecyl-trichlorosilane)-covered silicas (fused silica, quartz 0001) prepared under identical conditions. Streaming current measurements on the fused silica supported OTS sample indicate a well reproducible IEP of 3.5. The major part of the study focused on the quartz 0001 supported sample with an IEP lower than that of the fused silica support and in agreement with that found in a spectroscopic study. The IEP in water (on addition of HCl) was found at around pH 3, and appeared to shift to lower values in three subsequent measurements. A final measurement after a separate series in KCl media gave the same IEP as obtained in the very first measurement, suggesting that the experiments did not significantly change the interfacial properties despite a large number of experiments. In one series of measurements care was taken to exclude any cations other than protons from the measurements, such that protons are the only counter-ions to the negative net charge. While our IEPs with the quartz support agree well with recent estimates from sum frequency generation (SFG) investigations, none of the zeta-potential vs pH curves would mimic a pattern experimentally observed in the amplitude of the “ice-like” water band between pH 3.5 and 5 in that SFG study. Furthermore, our results do not indicate any significant chloride-ion adsorption in KCl systems, but instead the shift of the IEP with increasing KCl to higher pH values rather indicates specific effects of potassium ions. Under conditions more relevant to the spectroscopic study (i.e. in absence of potassium) no specific pattern reminiscent of the SFG results was found. When tested it was found that surface conductivity was negligible. 相似文献
128.
Chahinez Aouf Christine Le Guernevé Sylvain Caillol Hélène Fulcrand 《Tetrahedron》2013,69(4):1345-1353
The O-alkylation reaction by epichlorohydrin of some natural phenolic compounds such as 4-methylcatechol, gallic acid, protocatechuic acid, pyrogallol and resorcinol was investigated. Phenolic compounds reacted first with epichlorohydrin in the presence of benzyltriethylammonium chloride as phase transfer catalyst. Then, an aqueous solution of sodium hydroxide was added.It was demonstrated that the two competitive mechanisms involved in the O-alkylation reaction were highly dependent of the starting material. The O-alkylated products obtained in this reaction could be further used as bisphenol A substitutes in the synthesis of epoxy resins pre-polymers. 相似文献
129.
130.