全文获取类型
收费全文 | 2294篇 |
免费 | 141篇 |
国内免费 | 8篇 |
专业分类
化学 | 1878篇 |
晶体学 | 14篇 |
力学 | 28篇 |
数学 | 233篇 |
物理学 | 187篇 |
无线电 | 103篇 |
出版年
2023年 | 41篇 |
2022年 | 74篇 |
2021年 | 88篇 |
2020年 | 101篇 |
2019年 | 70篇 |
2018年 | 40篇 |
2017年 | 44篇 |
2016年 | 93篇 |
2015年 | 96篇 |
2014年 | 90篇 |
2013年 | 134篇 |
2012年 | 169篇 |
2011年 | 210篇 |
2010年 | 116篇 |
2009年 | 95篇 |
2008年 | 147篇 |
2007年 | 121篇 |
2006年 | 112篇 |
2005年 | 90篇 |
2004年 | 83篇 |
2003年 | 61篇 |
2002年 | 44篇 |
2001年 | 19篇 |
2000年 | 11篇 |
1999年 | 12篇 |
1998年 | 11篇 |
1997年 | 8篇 |
1996年 | 19篇 |
1995年 | 8篇 |
1994年 | 13篇 |
1993年 | 14篇 |
1992年 | 8篇 |
1991年 | 10篇 |
1990年 | 7篇 |
1988年 | 10篇 |
1987年 | 8篇 |
1985年 | 14篇 |
1984年 | 12篇 |
1983年 | 5篇 |
1982年 | 18篇 |
1981年 | 8篇 |
1980年 | 7篇 |
1979年 | 12篇 |
1978年 | 7篇 |
1977年 | 6篇 |
1976年 | 15篇 |
1975年 | 5篇 |
1974年 | 5篇 |
1973年 | 9篇 |
1972年 | 5篇 |
排序方式: 共有2443条查询结果,搜索用时 15 毫秒
171.
Using the chiral phosphoramidite ligand (S,R,R)-L1 in the conjugate addition of dimethylzinc to acyclic unsaturated malonates, enantioselectivities of up to 98% have been obtained for the first time. An iterative and stereodivergent route to 3,5-dimethyl esters that takes advantage of this asymmetric catalysis has been developed. 相似文献
172.
Cowley AR Dilworth JR Donnelly PS Gee AD Heslop JM 《Dalton transactions (Cambridge, England : 2003)》2004,(16):2404-2412
A series of copper(II) and nickel(II) 1,3-bis(thiosemicarbazonato) complexes have been synthesised by the reaction of the metal acetates with pyrazoline proligands. In each case the complexes have an overall neutral charge with a dianionic ligand. The copper 1,3-bis(4-methyl-3-thiosemicarbazonato complex has been characterised by X-ray crystallography, which shows the copper is in an essentially square-planar symmetric N(2)S(2) environment. The nickel 1,3-bis(4-methyl-3-thiosemicarbazonato) and nickel 1,3-bis(4-phenyl-3-thiosemicarbazonato) complexes have been characterised by X-ray crystallography and show that in these cases the nickel is in a distorted square-planar environment, but the bonding mode of the ligands is unusual; the nickel binds to one of the aza-methinic nitrogen atoms and one hydrazinic nitrogen, creating one five-membered N-N-C-S-Ni chelate ring and one four-membered N-C-S-Ni chelate ring. Interestingly, the X-ray structure of the ethyl analogue [1,3-bis(4-ethyl-3-thiosemicarbazonato)nickel(II)] shows that in this case the nickel is symmetrically coordinated in the usual manner. The nickel complexes are diamagnetic and the different coordination modes are confirmed in solution by NMR spectroscopy. The complexes are susceptible to oxidation in air and a nickel complex, in which the central methylene carbon has been oxidised, has been characterised by X-ray crystallography and NMR spectroscopy. Electrochemical measurements show that the copper complexes undergo a reversible one-electron reduction at biologically accessible potentials. 相似文献
173.
To enrich the limited set of isonitriles typically employed, 4-isocyano-2,2,6,6-teramethylpiperidin-1-oxyl (1) is proposed as an isonitrile bearing a nitroxyl moiety. Isocyanide 1 was used in some reactions characteristic of isonitriles. Isoselenocyanate, amides (products of Passerini and Ugi reactions), and tetrazole derivative were obtained. The EPR spectra of the urea derivative 5b and a product of an Ugi reaction 7 (both dinitroxides) were analyzed. [structure: see text] 相似文献
174.
Simulations show that, when a phase-separated binary AB fluid is driven to flow past chemically patterned substrates in a microchannel, the fluid exhibits unique morphological instabilities. For the pattern studied, these instabilities give rise to the simultaneous, periodic formation of monodisperse droplets of A in B and B in A. The system bifurcates between time-independent behavior and different types of regular, nondecaying oscillations in the structural characteristics. The surprisingly complex behavior is observed even in the absence of hydrodynamic interactions and arises from the interplay between the fluid flow and patterned substrate, which introduces nonlinearity into the dynamical system. 相似文献
175.
Clark RD Kar J Akella L Soltanshahi F 《Journal of chemical information and computer sciences》2003,43(3):829-836
Optimizable k-dissimilarity (OptiSim) selection entails drawing a series of subsamples of size k from a population and choosing the "best" candidate from each such subsample for inclusion in the selection set. By varying the size of the subsample, one can control the balance between representativeness and diversity in the selection set obtained. In the original formulation, a uniform random sampling from among valid candidates was used to draw the subsamples from a single target population. Here we describe in detail two key modifications that serve to extend the OptiSim methodology to vector selection for interdependent variables, specifically as applied to the design of combinatorial sublibraries. The first modification involves pivoting between variables: subsamples are drawn from each reagent pool in turn, with the viability of each candidate being evaluated in isolation as well as in terms of the products it will produce from complementary reagents already selected. The filters applied may be static or dynamic in nature, with molecular weight and hydrophobicity being examples of the former and structural diversity with respect to reagents already selected being an example of the latter. The second key modification is adding the ability to bias the selection of candidate reagents for inclusion in the subsamples. Taken together, these modifications support the efficient generation of multiblock and other sparse matrix designs that are both representative and diverse, and for which "backfilling" of designs edited to remove undesirable reagents or products is straightforward. The method is intrinsically fast and efficient, since enumeration of the full combinatorial is not required- only those candidates actually considered for inclusion need be evaluated. Moreover, because the subsample selection step is separate from the diversity-based selection of the "best" candidate, incorporating such bias in favor of a competing criterion such as low price provides a "natural," nonparametric mechanism for generating designs that are likely to be "good" in a double-objective, Pareto sense. 相似文献
176.
In the absence of added base, a deep navy-blue dimeric copper complex [CuII(H2L)(MeCN)]2(BF4)4 (1) of the non-deprotonated bis-terdentate diamide ligand H2L self-assembles whereas in the presence of base a grass-green [2 x 2] grid complex [CuII(HL)]4(BF4)4 (2) of the monodeprotonated ligand HL-, a rare example of a discrete grid of pyrazine-bridged metal ions, is formed. 相似文献
177.
Spatial patterning of thin polyacrylamide films bonded to self-assembled monolayers on silica microchannels is described as a means for manipulating cell-adhesion and electroosmotic properties in microchips. Streaming potential measurements indicate that the zeta potential is reduced by at least two orders of magnitude at biological pH, and the adhesion of several kinds of cells is reduced by 80-100%. Results are shown for cover slides and in wet-etched silica microchannels. Because the polyacrylamide film is thin and transparent, this film is consistent with optical manipulation of cells and detection of cell contents. The spatial patterning technique is straightforward and has the potential to aid on-chip analysis of single adherent cells. 相似文献
178.
Complexes of Ga3+, a d10 metal ion which lacks ligand-field-stabilization energy, are considered labile. In fact, hexaaquagallium(III) has a ligand exchange rate of 403 s-1, 2.5 times that of the analagous Fe3+ complex (Hugi-Cleary, D.; Helm, L.; Merbach, A. E. J. Am. Chem. Soc. 1987, 109, 4444-4450). Given this lability, resolution of Ga3+ complexes should be impossible. Despite this, we report the resolution of the Lambda and Delta isomers of tris(benzohydroxamate)gallium (III) (1), the first resolution of a mononuclear gallium complex. Not only is resolution possible, but these resolved complexes show remarkable resistance to racemization in aprotic solvents. The unprecedented stability of Lambda- and Delta-1 is a surprise, and as such, alters our understanding of classical coordination chemistry. 相似文献
179.
Lainton JA Allen MC Burton M Cameron S Edwards TR Harden G Hogg R Leung W Miller S Morrish JJ Rooke SM Wendt B 《Journal of combinatorial chemistry》2003,5(4):400-407
Efficient and general procedures have been developed for the solution-phase preparation of substituted morpholine derivatives, and a library has been produced around generic structure 1. This library was designed with proprietary modeling software for use as a general screening library. The 30 R1 reagents were phenols, and the 275 R2 reagents were taken from five different reagent classes, giving a variety of product classes in the final library of 8250 potential products. All of the library members were generated from a common intermediate, mesylate (5), which was synthesized efficiently, in bulk, in three steps from N-benzylethanolamine (2). High-throughput chemistry using robotics was carried out to produce the 7907 library members, which were individually characterized by reversed-phase LC/MS analysis. 相似文献
180.
Dolan J 《Analytical and bioanalytical chemistry》2003,376(8):1168-1171
The forensic discipline of ignitable liquid and fire debris analysis is rapidly changing. Refinements in existing methods as well as development of new techniques are changing the routine methods of analysis. Optimization of existing extraction techniques and research into novel methods of extracting debris have improved the recovery of ignitable liquids from debris samples. The application of highly specialized instrumentation to problems of sensitivity and matrix interference has resulted in new ways of performing chemical analyses, allowing for improved limits of detection. Preliminary research in novel approaches to ignitable liquid comparisons is being evaluated, with the hopes of providing more detailed information to the field investigators. Research into a variety of areas related to fire debris analysis is ongoing, and will continue to improve the quality of ignitable liquid residue analysis. 相似文献