全文获取类型
收费全文 | 781篇 |
免费 | 18篇 |
国内免费 | 6篇 |
专业分类
化学 | 552篇 |
晶体学 | 2篇 |
力学 | 17篇 |
数学 | 145篇 |
物理学 | 89篇 |
出版年
2020年 | 8篇 |
2019年 | 13篇 |
2018年 | 4篇 |
2016年 | 12篇 |
2015年 | 18篇 |
2014年 | 16篇 |
2013年 | 28篇 |
2012年 | 30篇 |
2011年 | 43篇 |
2010年 | 32篇 |
2009年 | 22篇 |
2008年 | 39篇 |
2007年 | 31篇 |
2006年 | 39篇 |
2005年 | 25篇 |
2004年 | 26篇 |
2003年 | 27篇 |
2002年 | 21篇 |
2001年 | 20篇 |
2000年 | 19篇 |
1999年 | 10篇 |
1998年 | 16篇 |
1997年 | 15篇 |
1996年 | 7篇 |
1995年 | 11篇 |
1994年 | 15篇 |
1993年 | 11篇 |
1992年 | 10篇 |
1991年 | 9篇 |
1990年 | 9篇 |
1989年 | 8篇 |
1988年 | 8篇 |
1987年 | 12篇 |
1985年 | 13篇 |
1984年 | 14篇 |
1983年 | 11篇 |
1982年 | 8篇 |
1981年 | 12篇 |
1980年 | 13篇 |
1979年 | 6篇 |
1978年 | 9篇 |
1977年 | 13篇 |
1976年 | 5篇 |
1975年 | 6篇 |
1973年 | 4篇 |
1972年 | 8篇 |
1970年 | 5篇 |
1968年 | 5篇 |
1967年 | 5篇 |
1926年 | 7篇 |
排序方式: 共有805条查询结果,搜索用时 0 毫秒
11.
Sm(II)-modified periodic mesoporous silica (PMS), Sm[N(SiHMe2)2]2(THF)x@MCM-41, was used for the synthesis of Sm(II) alkyl, alkoxide, and indenyl surface species via secondary ligand exchange. The performance of the novel Sm(II)-based organometallic–inorganic hybrid materials as initiators for the graft polymerization of methyl methacrylate (MMA) is reported. All of the Sm(II) hybrid materials including the new PMMA–PMS composites were characterized via N2 physisorption, elemental analysis, FTIR spectroscopy, and scanning electron microscopy (SEM). The organic–inorganic composites revealed complete pore blockage as well as enrichment and strong adhesion of the polymer at the exterior of the porous silica material. 相似文献
12.
The "epimerisation" of UDP-GlcNAc to ManNAc, the first step in the biosynthesis of sialic acids, is catalyzed by UDP-GlcNAc 2-epimerase. In this paper we report the synthesis of transition state based inhibitors of this enzyme. To mimic the assumed first transition state of this reaction (TS 1), we designed and synthesized the novel UDP-exo-glycal derivatives 1-4. We also report herein the synthesis of 5 and 6, the first C-glycosidic derivatives of 2-acetamidoglucal, and the synthesis of the ketosides 7 and 8, which were designed as bis-substrate analogue and bis- product analogue, respectively, to mimic the second step of the reaction via the assumed second transition state TS 2. 相似文献
13.
Alicia Reyes-Arellano Roland Boese Ingo Steller Reiner Sustmann 《Structural chemistry》1995,6(6):391-396
The crystal structures of molecular complexes betweenmeso- 1,2-diphenyl-1,2-ethanediol and two bisimines (N,N-(dibenzylidene)-ethylenediamine and glyoxylidene-bis(2,4-dimethyl-3-pentyl-amine) are reported at different temperatures. The structure-determining motif of the cocrystalline arrangement is one single O-H . N hydrogen bond resulting in infinite ladderlike polymers. The supramolecular structure is formed by recognition of fitting species: Thed- orl-isomers do not arrange in such structures.1H NMR experiments show that no prearrangements take place by forming complexes in solution. 相似文献
14.
Xu Y Eilers G Borgström M Pan J Abrahamsson M Magnuson A Lomoth R Bergquist J Polívka T Sun L Sundström V Styring S Hammarström L Akermark B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(24):7305-7314
To mimic the electron-donor side of photosystem II (PSII), three trinuclear ruthenium complexes (2, 2a, 2b) were synthesized. In these complexes, a mixed-valent dinuclear Ru2(II,III) moiety with one phenoxy and two acetato bridges is covalently linked to a Ru(II) tris-bipyridine photosensitizer. The properties and photoinduced electron/energy transfer of these complexes were studied. The results show that the Ru2(II,III) moieties in the complexes readily undergo reversible one-electron reduction and one-electron oxidation to give the Ru2(II,III) and Ru2(III,III) states, respectively. This could allow for photooxidation of the sensitizer part with an external acceptor and subsequent electron transfer from the dinuclear ruthenium moiety to regenerate the sensitizer. However, all trinuclear ruthenium complexes have a very short excited-state lifetime, in the range of a few nanoseconds to less than 100 ps. Studies by femtosecond time-resolved techniques suggest that a mixture of intramolecular energy and electron transfer between the dinuclear ruthenium moiety and the excited [Ru(bpy)3]2+ photosensitizer is responsible for the short lifetimes. This problem is overcome by anchoring the complexes with ester- or carboxyl-substituted bipyridine ligands (2a, 2b) to nanocrystalline TiO2, and the desired electron transfer from the excited state of the [Ru(bpy)3]2+ moiety to the conduction band of TiO2 followed by intramolecular electron transfer from the dinuclear Ru2(II,III) moiety to photogenerated Ru(III) was observed. The resulting long-lived Ru2(III,III) state decays on the millisecond timescale. 相似文献
15.
In the temperature range from 950 to 1200 K Kp-values result from 5 · 10−5 to 6,9 · 10−3 for the heterogeneous reversible reaction Ge(s) + H2O(g) ⇋ GeO(g) + H2O(g), the average reaction enthalpy being 46,5 ± 05 kcal/mol. Etching rates calculated with these equilibrium constants for closed systems are 20-25% larger than the experimental etching rates for (110)-Ge in the sandwich device. The ratio of the etching rates is for (111)-, (100)- and (110)-Ge 1:1,4:1,8; the average reaction enthalpy calculated experimentally is 46 ± 1 kcal/mol for the temperature range 1000-1200 K. The dependence of transport rate on distance between source and substrate characterizes the sandwich device as a quasi-closed system with the diffusion as the rate controlling step of the material transport. 相似文献
16.
17.
N‐aroyl‐N′‐arylsulfonylhydrazines can be obtained by oxidation of aromatic aldehyde N‐arylsulfonylhydrazones with bis(trifluoroacetoxy)iodobenzene in acetone at room temperature in mild to good yields. 相似文献
18.
Prof. Dr. Lutz F. Tietze Dr. Ling Ma Johannes R. Reiner Stefan Jackenkroll Sven Heidemann 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(26):8610-8614
Blennolide A can be synthesized through an enantioselective domino‐Wacker/carbonylation/methoxylation reaction of 7 a with 96 % ee and an enantioselective Wacker oxidation of 7 b with 89 % ee. Further transformations led to the α,β‐unsaturated ester (E)‐ 17 , which was subjected to a highly selective Michael addition, introducing a methyl group to give 18 a . After a threefold oxidation and an intramolecular acylation, the tetrahydroxanthenone 4 was obtained, which could be transformed into (?)‐blennolide A (ent‐ 1 ) in a few steps. 相似文献
19.
Dennis A. Buschmann Dr. H. Martin Dietrich Dr. David Schneider Dr. Verena M. Birkelbach Dr. Christoph Stuhl Prof. Dr. Karl W. Törnroos Dr. Cäcilia Maichle-Mössmer Prof. Dr. Reiner Anwander 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(47):10834-10840
Tetramethylaluminato/halogenido(X) ligand exchange reactions in half-sandwich complexes [CpRLa(AlMe4)2] are feasible in non-coordinating solvents and provide access to large coordination clusters of the type [CpRLaX2]x. Incomplete exchange reactions generate the hexalanthanum clusters [CpR6La6X8(AlMe4)4] (CpR=Cp*=C5Me5, X=I; CpR=Cp′=C5H4SiMe3, X=Br, I). Treatment of [Cp*La(AlMe4)2] with two equivalents Me3SiI gave the nonalanthanum cluster [Cp*LaI2]9, while the exhaustive reaction of [Cp′La(AlMe4)2] with the halogenido transfer reagents Me3GeX and Me3SiX (X=I, Br, Cl) produced a series of monocyclopentadienyl rare-earth-metal clusters with distinct nuclearity. Depending on the halogenido ion size the homometallic clusters [Cp′LaCl2]10 and [Cp′LaX2]12 (X=Br, I) could be isolated, whereas different crystallization techniques led to the aggregation of clusters of distinct structural motifs, including the desilylated cyclopentadienyl-bridged cluster [(μ-Cp)2Cp′8La8I14] and the heteroaluminato derivative [Cp′10La10Br18(AlBr2Me2)2]. The use of the Cp′ ancillary ligand facilitates cluster characterization by means of NMR spectroscopy. 相似文献
20.
Adsorption, desorption, and surface-promoted hydrolysis of glucose-1-phosphate in aqueous goethite (α-FeOOH) suspensions 总被引:2,自引:0,他引:2
Olsson R Giesler R Loring JS Persson P 《Langmuir : the ACS journal of surfaces and colloids》2010,26(24):18760-18770
Adsorption, desorption, and precipitation reactions at environmental interfaces govern the fate of phosphorus in terrestrial and aquatic environments. Typically, a substantial part of the total pool of phosphorus consists of organophosphate, and in this study we have focused on the interactions between glucose-1-phosphate (G1P) and goethite (α-FeOOH) particles. The adsorption and surface-promoted hydrolysis reactions have been studied at room temperature as a function of pH, time, and total concentration of G1P by means of quantitative batch experiments in combination with infrared spectroscopy. A novel simultaneous infrared and potentiometric titration (SIPT) technique has also been used to study the rates and mechanisms of desorption of the surface complexes. The results have shown that G1P adsorption occurs over a wide pH interval and at pH values above the isoelectric point of goethite (IEP(goethite) = 9.4), indicating a comparatively strong interaction with the particle surfaces. As evidenced by IR spectroscopy, G1P formed pH-dependent surface complexes on goethite, and investigations of both adsorption and desorption processes were consistent with a model including three types of surface complexes. These complexes interact monodentately with surface Fe but differ in hydrogen bonding interactions via the auxiliary oxygens of the phosphate group. The apparent desorption rates were shown to be influenced by reaction pathways that include interconversion of surface species, which highlights the difficulty in determining the intrinsic desorption rates of individual surface complexes. Desorption results have also indicated that the molecular structures of surface complexes and the surface charge are two important determinants of G1P desorption rates. Finally, this study has shown that surface-promoted hydrolysis of G1P by goethite is base-catalyzed but that the extent of hydrolysis was small. 相似文献