全文获取类型
收费全文 | 370篇 |
免费 | 35篇 |
国内免费 | 4篇 |
专业分类
化学 | 282篇 |
晶体学 | 2篇 |
力学 | 14篇 |
数学 | 39篇 |
物理学 | 72篇 |
出版年
2024年 | 2篇 |
2023年 | 12篇 |
2022年 | 10篇 |
2021年 | 20篇 |
2020年 | 11篇 |
2019年 | 15篇 |
2018年 | 17篇 |
2017年 | 6篇 |
2016年 | 28篇 |
2015年 | 17篇 |
2014年 | 14篇 |
2013年 | 33篇 |
2012年 | 29篇 |
2011年 | 41篇 |
2010年 | 16篇 |
2009年 | 13篇 |
2008年 | 26篇 |
2007年 | 18篇 |
2006年 | 16篇 |
2005年 | 16篇 |
2004年 | 8篇 |
2003年 | 5篇 |
2002年 | 6篇 |
2001年 | 6篇 |
2000年 | 3篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1997年 | 3篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1993年 | 1篇 |
1991年 | 2篇 |
1988年 | 1篇 |
1987年 | 1篇 |
1985年 | 1篇 |
1975年 | 2篇 |
1974年 | 3篇 |
1972年 | 1篇 |
1926年 | 1篇 |
1896年 | 1篇 |
排序方式: 共有409条查询结果,搜索用时 311 毫秒
401.
Laurence Piche Jean‐Christophe Daigle Gregor Rehse Prof. Jerome P. Claverie 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(11):3277-3285
Palladium phosphanesulfonate [R2P(C6H4‐o‐SO3)PdMeL] catalysts permit the copolymerization of an exceptional large number of functional olefins with ethylene. However, these catalysts usually have reduced activity. We here have conducted a systematic study on the influence of the phosphane substituent, R, on activity and molecular weight. Phosphanes with strong σ‐donating character are shown to lead to the most active catalysts. Thus, the catalyst based on phosphane bis‐tert‐butyl‐phosphanyl‐benzenesulfonic acid (R=tBu) exhibits unprecedented high activity, rapidly polymerizing ethylene at room temperature to yield a linear polymer of high molecular weight (Mw=116 000 g mol?1). The influence of the R group on the catalyst ability to incorporate methyl acrylate is also investigated. 相似文献
402.
Levine DR Caruso A Siegler MA Tovar JD 《Chemical communications (Cambridge, England)》2012,48(50):6256-6258
The synthesis of new boron-containing acenes (meta-B-entacenes) is reported. These compounds exhibit slightly non-planar core geometries with blue-shifted spectral properties and more negative electrochemical reduction potentials relative to known para isomers. Polarizable π-extended architectures were realized via cross-coupling procedures with chloro-functionalized precursors. 相似文献
403.
Sanguinet L Pozzo JL Guillaume M Champagne B Castet F Ducasse L Maury E Soulié J Mançois F Adamietz F Rodriguez V 《The journal of physical chemistry. B》2006,110(22):10672-10682
This paper presents a series of acidoswitchable NLO-phores combining the 9-methylbenzimidazolo[2,3-b]oxazolidine core with various pi systems such as phenylethenyl, phenylethynyl, and naphthylethenyl. All the prepared derivatives are shown to display acidochromic behavior at ambient temperature. The remarkable contrast in the NLO response along the reversible transformations observed in HRS experiments is rationalized by high level theoretical calculations. 相似文献
404.
405.
Trinuclear copper(II) complex [CuII3(NIT2PhO)2Cl4] was synthesized with p-cresol-substituted bis(α-nitronyl nitroxide) biradical: 4-methyl-2,6-bis(1-oxyl-3-oxido-4,4,5,5-tetramethyl-2-imidazolin-2-yl)phenol (NIT2PhOH). The crystal structure of this heterospin complex was determined using single-crystal X-ray diffraction analysis and exhibits four unusual seven-membered metallocycles formed from the coordination of oxygen atoms of the N-O groups and of bridging phenoxo (µ-PhO−) moieties with copper(II) ions. The crystal structure analysis reveals an incipient agostic interaction between a square planar copper center and a hydrogen-carbon bond from one methyl group carried on the coordinated nitronyl-nitroxide radical. The intramolecular Cu∙∙∙H-C interaction involves a six-membered metallocycle and may stabilize the copper center in square planar coordination mode. From the magnetic susceptibility measurements, the complex, which totals seven S = 1/2 spin carriers, has almost a ground state spin S = 1/2 at room temperature ascribed to strong antiferromagnetic interaction between the nitronyl nitroxide moieties and the copper(II) centers and in between the copper(II) centers through the bridging phenoxo oxygen atom. 相似文献
406.
Kim Anh Nguyen Emilie Lesur Maxime Ribéraud Antoine Sallustrau Davide Audisio Frédéric Taran 《Helvetica chimica acta》2023,106(3):e202200187
The synthesis of four clickable sydnone-heptamethine cyanine derivatives is described in this article. The synthetic route is based on a palladium-cross coupling reactions of sydnone boronates affording the desired sydnone-cyanine conjugates in only five steps. These compounds were shown to react smoothly with cyclooctynes to form the corresponding pyrazoles clicked products quantitatively at room temperature and with rate constants up to 18 m −1 ⋅ s−1, affording interesting new tools for biorthogonal fluorescent labelling of (bio)molecules. Fluorescence properties of both sydnone- and pyrazole-cyanines are described, as well. 相似文献
407.
Alexandre Labiche Augustin Malandain Maxime Molins Dr. Frédéric Taran Dr. Davide Audisio 《Angewandte Chemie (International ed. in English)》2023,62(36):e202303535
In contrast to stable and natural abundant carbon-12, the synthesis of organic molecules with carbon (radio)isotopes must be conceived and optimized in order to navigate through the hurdles of radiochemical requirements, such as high costs of the starting materials, harsh conditions and radioactive waste generation. In addition, it must initiate from the small cohort of available C-labeled building blocks. For long time, multi-step approaches have represented the sole available patterns. On the other side, the development of chemical reactions based on the reversible cleavage of C−C bonds might offer new opportunities and reshape retrosynthetic analysis in radiosynthesis. This review aims to provide a short survey on the recently emerged carbon isotope exchange technologies that provide effective opportunity for late-stage labeling. At present, such strategies have relied on the use of primary and easily accessible radiolabeled C1-building blocks, such as carbon dioxide, carbon monoxide and cyanides, while the activation principles have been based on thermal, photocatalytic, metal-catalyzed and biocatalytic processes. 相似文献
408.
Maxime Robin Stephane Mialhe Valerie Pique Robert Faure Jean‐Pierre Galy 《ChemInform》2002,33(38):153-153
409.