全文获取类型
收费全文 | 1129篇 |
免费 | 62篇 |
国内免费 | 4篇 |
专业分类
化学 | 927篇 |
晶体学 | 6篇 |
力学 | 10篇 |
数学 | 63篇 |
物理学 | 189篇 |
出版年
2023年 | 18篇 |
2022年 | 18篇 |
2021年 | 32篇 |
2020年 | 43篇 |
2019年 | 27篇 |
2018年 | 26篇 |
2017年 | 21篇 |
2016年 | 31篇 |
2015年 | 45篇 |
2014年 | 34篇 |
2013年 | 65篇 |
2012年 | 85篇 |
2011年 | 99篇 |
2010年 | 37篇 |
2009年 | 24篇 |
2008年 | 78篇 |
2007年 | 90篇 |
2006年 | 78篇 |
2005年 | 64篇 |
2004年 | 53篇 |
2003年 | 44篇 |
2002年 | 33篇 |
2001年 | 8篇 |
2000年 | 13篇 |
1999年 | 8篇 |
1998年 | 5篇 |
1997年 | 6篇 |
1996年 | 8篇 |
1995年 | 6篇 |
1994年 | 4篇 |
1993年 | 4篇 |
1992年 | 5篇 |
1991年 | 2篇 |
1990年 | 6篇 |
1989年 | 2篇 |
1988年 | 9篇 |
1987年 | 3篇 |
1986年 | 4篇 |
1985年 | 6篇 |
1984年 | 2篇 |
1982年 | 2篇 |
1981年 | 5篇 |
1980年 | 9篇 |
1979年 | 5篇 |
1978年 | 9篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1973年 | 3篇 |
1939年 | 1篇 |
1893年 | 1篇 |
排序方式: 共有1195条查询结果,搜索用时 15 毫秒
41.
42.
43.
Li T Garg U Liu Y Marks R Nayak BK Rao PV Fujiwara M Hashimoto H Kawase K Nakanishi K Okumura S Yosoi M Itoh M Ichikawa M Matsuo R Terazono T Uchida M Kawabata T Akimune H Iwao Y Murakami T Sakaguchi H Terashima S Yasuda Y Zenihiro J Harakeh MN 《Physical review letters》2007,99(16):162503
The strength distributions of the giant monopole resonance (GMR) have been measured in the even-A Sn isotopes (A=112-124) with inelastic scattering of 400-MeV alpha particles in the angular range 0 degrees -8.5 degrees . We find that the experimentally observed GMR energies of the Sn isotopes are lower than the values predicted by theoretical calculations that reproduce the GMR energies in 208Pb and 90Zr very well. From the GMR data, a value of Ktau = -550 +/- 100 MeV is obtained for the asymmetry term in the nuclear incompressibility. 相似文献
44.
Kaitlyn A. Perez Cameron R. Rogers Emily A. Weiss 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(33):14195-14199
This Communication describes the use of CuInS2/ZnS quantum dots (QDs) as photocatalysts for the reductive deprotection of aryl sulfonyl-protected phenols. For a series of aryl sulfonates with electron-withdrawing substituents, the rate of deprotection for the corresponding phenyl aryl sulfonates increases with decreasing electrochemical potential for the two electron transfers within the catalytic cycle. The rate of deprotection for a substrate that contains a carboxylic acid, a known QD-binding group, is accelerated by more than a factor of ten from that expected from the electrochemical potential for the transformation, a result that suggests that formation of metastable electron donor–acceptor complexes provides a significant kinetic advantage. This deprotection method does not perturb the common NHBoc or toluenesulfonyl protecting groups and, as demonstrated with an estrone substrate, does not perturb proximate ketones, which are generally vulnerable to many chemical reduction methods used for this class of reactions. 相似文献
45.
Manolo C. Per Emily K. Fletcher Ellen T. Swann Deidre M. Cleland 《Journal of computational chemistry》2020,41(27):2378-2382
We assess the performance of variational (VMC) and diffusion (DMC) quantum Monte Carlo methods for calculating the radical stabilization energies of a set of 43 carbon-centered radical species. Even using simple single-determinant trial wavefunctions, both methods perform exceptionally well, with mean absolute deviations from reference values well under the chemical accuracy standard of 1 kcal/mol. In addition, the use of DMC results in a highly concentrated spread of errors, with all 43 results within chemical accuracy at the 95% confidence level. These results indicate that DMC is an extremely reliable method for calculating radical stabilization energies and could be used as a benchmark method for larger systems in future. 相似文献
46.
Yongfeng Li Chaoji Chen Jianwei Song Chunpeng Yang Yudi Kuang Azhar Vellore Emily Hitz Mingwei Zhu Feng Jiang Yonggang Yao Amy Gong Ashlie Martini Liangbing Hu 《中国化学》2020,38(8):823-829
Lightweight structural materials are important for the energy efficiency of applications, particularly those in the building sector. Here, inspired by nature, we developed a strong, superhydrophobic, yet lightweight material by simple in situ growth of nano‐SiO2 and subsequent densification of the wood substrate. In situ generation of SiO2 nanoparticles both inside the wood channels and on the wood surfaces gives the material superhydrophobicity, with static and dynamic contact angles of 159.4o and 3o, respectively. Densification of the wood to remove most of the spaces among the lumen and cell walls results in a laminated, dense structure, with aligned cellulose nanofibers, which in turn contributes to a high mechanical strength up to 384.2 MPa (7‐times higher than natural wood). Such treatment enables the strong and superhydrophobic wood (SH‐Wood) to be stable and have excellent water, acid, and alkaline resistance. The high mechanical strength of SH‐Wood combined with its excellent structural stability in harsh environments, as well its low density, positions the strong and superhydrophobic wood as a promising candidate for strong, lightweight, and durable structural materials that could potentially replace steel. 相似文献
47.
Luminescent quantum dots (QDs) are colloidal semiconductor nanocrystals consisting of an inorganic core covered by a molecular layer of organic surfactants. Although QDs have been known for more than thirty years, they are still attracting the interest of researchers because of their unique size-tunable optical and electrical properties arising from quantum confinement. Moreover, the controlled decoration of the QD surface with suitable molecular species enables the rational design of inorganic-organic multicomponent architectures that can show a vast array of functionalities. This minireview highlights the recent progress in the use of surface-modified QDs – in particular, those based on cadmium chalcogenides – as supramolecular platforms for light-related applications such as optical sensing, triplet photosensitization, photocatalysis and phototherapy. 相似文献
48.
Emily B. Corcoran Jonathan P. McMullen Franois Lvesque Michael K. Wismer John R. Naber 《Angewandte Chemie (International ed. in English)》2020,59(29):11964-11968
With the development of new photocatalytic methods over recent decades, the translation of these chemical reactions to industrial‐production scales using continuous‐flow reactors has become a topic of increasing interest. In this context, we describe our studies toward elucidating an empirically derived parameter for scaling photocatalytic reactions in flow. By evaluating the performance of a photocatalytic C?N cross‐coupling reaction across multiple reactor sizes and geometries, it was demonstrated that expressing product yield as a function of the absorbed photon equivalents provides a predictive, empirical scaling parameter. Through the use of this scaling factor and characterization of the photonic flux within each reactor, the cross‐coupling was scaled successfully from the milligram scale in batch to a multi‐kilogram reaction in flow. 相似文献
49.
Kaitlyn A. Perez Cameron R. Rogers Emily A. Weiss 《Angewandte Chemie (International ed. in English)》2020,59(33):14091-14095
This Communication describes the use of CuInS2/ZnS quantum dots (QDs) as photocatalysts for the reductive deprotection of aryl sulfonyl‐protected phenols. For a series of aryl sulfonates with electron‐withdrawing substituents, the rate of deprotection for the corresponding phenyl aryl sulfonates increases with decreasing electrochemical potential for the two electron transfers within the catalytic cycle. The rate of deprotection for a substrate that contains a carboxylic acid, a known QD‐binding group, is accelerated by more than a factor of ten from that expected from the electrochemical potential for the transformation, a result that suggests that formation of metastable electron donor–acceptor complexes provides a significant kinetic advantage. This deprotection method does not perturb the common NHBoc or toluenesulfonyl protecting groups and, as demonstrated with an estrone substrate, does not perturb proximate ketones, which are generally vulnerable to many chemical reduction methods used for this class of reactions. 相似文献
50.
Emily Kerr David J. Hayne Lachlan C. Soulsby Joseph C. Bawden Steven J. Blom Egan H. Doeven Luke C. Henderson Conor F. Hogan Paul S. Francis 《Chemical science》2022,13(2):469
The classic and most widely used co-reactant electrochemiluminescence (ECL) reaction of tris(2,2′-bipyridine)ruthenium(ii) ([Ru(bpy)3]2+) and tri-n-propylamine is enhanced by an order of magnitude by fac-[Ir(sppy)3]3− (where sppy = 5′-sulfo-2-phenylpyridinato-C2,N), through a novel ‘redox mediator’ pathway. Moreover, the concomitant green emission of [Ir(sppy)3]3−* enables internal standardisation of the co-reactant ECL of [Ru(bpy)3]2+. This can be applied using a digital camera as the photodetector by exploiting the ratio of R and B values of the RGB colour data, providing superior sensitivity and precision for the development of low-cost, portable ECL-based analytical devices.A water-soluble Ir(iii) complex is shown to enhance the ‘remote’ mechanism of the most widely used co-reactant ECL reaction of tris(2,2′-bipyridine)ruthenium(ii) with tripropylamine. 相似文献