全文获取类型
收费全文 | 1774篇 |
免费 | 82篇 |
国内免费 | 18篇 |
专业分类
化学 | 1233篇 |
晶体学 | 11篇 |
力学 | 53篇 |
数学 | 275篇 |
物理学 | 302篇 |
出版年
2023年 | 10篇 |
2022年 | 20篇 |
2021年 | 41篇 |
2020年 | 33篇 |
2019年 | 23篇 |
2018年 | 27篇 |
2017年 | 33篇 |
2016年 | 54篇 |
2015年 | 41篇 |
2014年 | 58篇 |
2013年 | 93篇 |
2012年 | 144篇 |
2011年 | 173篇 |
2010年 | 55篇 |
2009年 | 55篇 |
2008年 | 129篇 |
2007年 | 129篇 |
2006年 | 121篇 |
2005年 | 124篇 |
2004年 | 84篇 |
2003年 | 64篇 |
2002年 | 74篇 |
2001年 | 23篇 |
2000年 | 17篇 |
1999年 | 10篇 |
1998年 | 13篇 |
1997年 | 9篇 |
1996年 | 11篇 |
1995年 | 9篇 |
1994年 | 7篇 |
1993年 | 14篇 |
1992年 | 5篇 |
1991年 | 5篇 |
1990年 | 5篇 |
1989年 | 8篇 |
1988年 | 7篇 |
1987年 | 5篇 |
1985年 | 16篇 |
1984年 | 16篇 |
1983年 | 7篇 |
1982年 | 10篇 |
1981年 | 10篇 |
1980年 | 8篇 |
1979年 | 6篇 |
1978年 | 9篇 |
1977年 | 11篇 |
1976年 | 9篇 |
1975年 | 8篇 |
1974年 | 5篇 |
1973年 | 6篇 |
排序方式: 共有1874条查询结果,搜索用时 46 毫秒
71.
Abigail O. Delawder Anusree Natraj Nathan D. Colley Tiana Saak Angelique F. Greene 《Supramolecular chemistry》2019,31(8):523-531
ABSTRACTAlthough it is well known that viologen radical cations can self-assemble into stacks or complexes on account of radical-radical pairing interactions, it has only recently been demonstrated that reduction of main-chain polyviologens integrated into hydrogel networks can trigger actuation. In these earlier examples, hydrogels comprising oligoethylene glycol-based polyviologens and poly(ethylene glycol) were functionalized with terminal azide groups to prepare ‘click’-based gels. Here, we report a new structural design for the functional polyviologen that consists of main-chain viologen subunits separated by hexamethylene groups instead of glycols and is capped at each end with styrene groups. Activation of this viologen-based macrocrosslinker was achieved using chemical- and photoreduction methods and its ability to undergo intramolecular chain-folding was monitored by absorption spectroscopy. Acrylate-based organogels and hydrogels were also prepared and a comparison was carried out to assess the actuator performance in each gel in terms of the rate of contraction and changes in stiffness. 相似文献
72.
Dr. Aron J. Huckaba Dr. Aswani Yella Dr. Louis E. McNamara April E. Steen J. Scott Murphy Casey A. Carpenter George D. Puneky Prof. Nathan I. Hammer Prof. Mohammad Khaja Nazeeruddin Prof. Michael Grätzel Prof. Jared H. Delcamp 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(43):15536-15542
Desirable components for dye‐sensitzed solar cell (DSC) sensitizers and fluorescent imaging dyes include strong donating building blocks coupled with well‐balanced acceptor functionalities for absorption beyond the visible range. We have evaluated the effects of increasing acceptor strengths and incorporation of dye morphology controlling groups on molar absorptivity and absorption breadth with indolizine donor‐based dyes. Indolizine‐based D –A and D –π–A sensitizers incorporating bis‐rhodanine, tricyanofuran (TCF), and cyanoacrylic acid functionalities were analyzed for performance in DSC devices. The TCF derivatives were also evaluated as near‐infrared (NIR)‐emissive materials with the AH25 emissions extending past 1000 nm. 相似文献
73.
74.
Light-bullet routing and control is theoretically demonstrated in a slab waveguide architecture using a fully addressable electronic current injection mechanism for gain control. By exploiting gain mediated interactions between bullets, photonic NAND and NOR logic gates are produced on the same chip design. The robustness, simplicity, and control offered by light-bullets in slab waveguide architectures suggest that such devices should be seriously considered as candidates for technological development.
相似文献75.
Nathan Barker Nigel Boston Norbert Peyerimhoff Alina Vdovina 《Monatshefte für Mathematik》2012,3(2):319-327
We find new mixed and unmixed Beauville structures for groups constructed as 2-quotients, i.e. quotients of 2-power order, of the fundamental group of a certain simplicial complex. 相似文献
76.
Jose Castro‐Perez Nathan Hatcher Nana Kofi Karikari Sheng‐Ping Wang Vivienne Mendoza Henry Shion Alan Millar John Shockcor Mark Towers David McLaren Vinit Shah Stephen Previs Karen Akinsanya Michele Cleary Thomas P. Roddy Douglas G. Johns 《Rapid communications in mass spectrometry : RCM》2014,28(22):2471-2479
77.
78.
Justin J. Maresh Sonia E. Chavez Matthew J. Asciutto Nathan D. Brown Alexander A. Delgado Youya Gao 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(9):683-688
Electrophilic trisubstituted ethylenes, phenoxy ring-substituted methyl 2-cyano-3-phenyl-2-propenoates, RPhCH=C(CN)CO2CH3, where R is 4-(4-BrC6H5O), 2-(4-ClC6H5O), 3-(4-ClC6H5O), 4-(3-ClC6H5O), 4-(4-ClC6H5O), 4-(4-FC6H5O), 2-(3-CH3OC6H5O), 2-(4-CH3OC6H5O), 3-(4-CH3OC6H5O), 4-(4-CH3OC6H5O), 3-(4-CH3C6H5O) were prepared and copolymerized with styrene. The monomers were synthesized by the piperidine catalyzed Knoevenagel condensation of phenoxy ring-substituted benzaldehydes and methyl cyanoacetate, and characterized by CHN analysis, IR, 1H and 13C-NMR. All the ethylenes were copolymerized with styrene (M1) in solution with radical initiation (ABCN) at 70°C. The compositions of the copolymers were calculated from nitrogen analysis and the structures were analyzed by IR, 1H and 13C-NMR. The order of relative reactivity (1/r1) for the monomers is 4-(4-CH3OC6H5O) (6.07) > 3-(4-ClC6H5O) (3.38) > 3-(4-CH3OC6H5O) (2.78) > 4-(3-ClC6H5O) (2.77) > 2-(4-ClC6H5O) (2.29) > 3-(4-CH3C6H5O) (1.98) > 4-(4-FC6H5O) (1.92) > 4-(4-ClC6H5O) (1.89) > 2-(3-CH3OC6H5O) (1.39) > 2-(4-CH3OC6H5O) (0.90) > 4-(4-BrC6H5O) (0.77). Relatively high Tg of the copolymers in comparison with that of polystyrene indicates a decrease in chain mobility of the copolymer due to the high dipolar character of the trisubstituted ethylene monomer unit. Decomposition of the copolymers in nitrogen occurred in two steps, first in the 200-500°C range with residue (2.5-8.0% wt), which then decomposed in the 500-800°C range. 相似文献
79.
80.
Nathan J. Downs Peter W. Schouten Alfio V. Parisi 《Photochemistry and photobiology》2013,89(5):1234-1243
Fringing coral reefs provide a unique opportunity to study shallow aquatic ecosystems. A fringing coral reef system located in close proximity to a developed region was considered in this study. In such an environment, the rate of decay of dissolved organic matter is high and the penetration of higher energy ultraviolet‐B (UVB) extends a greater influence on species diversity, particularly upon shallow benthic communities. Results from a 9 month subsurface UVB exposure measurement campaign performed at a site located on the southern Queensland coast (Hervey Bay, 25°S) are presented in this research. For this, a novel dosimetric technique was utilized to measure long‐term subsurface UVB exposures. The resultant data set includes exposure measurements made during the significant La Niña event of late 2010 which resulted in unprecedented high sea surface temperatures and severe flooding across eastern Australia, impacting upon the lagoon regions of the Great Barrier Reef and Queensland's southern estuaries, including the study site. The influence of season, diurnal tidal variation, cloud cover and solar zenith angle were analyzed over the campaign period. Mean minimum daylight water depth was found to be the most significant factor influencing subsurface UVB. 相似文献