全文获取类型
收费全文 | 80篇 |
免费 | 0篇 |
专业分类
化学 | 58篇 |
数学 | 3篇 |
物理学 | 19篇 |
出版年
2023年 | 3篇 |
2021年 | 4篇 |
2020年 | 5篇 |
2019年 | 5篇 |
2018年 | 2篇 |
2017年 | 1篇 |
2014年 | 4篇 |
2013年 | 1篇 |
2012年 | 2篇 |
2011年 | 3篇 |
2010年 | 3篇 |
2009年 | 1篇 |
2007年 | 3篇 |
2006年 | 1篇 |
2005年 | 4篇 |
2004年 | 3篇 |
2003年 | 3篇 |
2002年 | 10篇 |
2001年 | 3篇 |
2000年 | 4篇 |
1999年 | 7篇 |
1998年 | 1篇 |
1994年 | 2篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1982年 | 1篇 |
1977年 | 1篇 |
排序方式: 共有80条查询结果,搜索用时 15 毫秒
31.
We have studied the peak effect (PE) phenomenon in single crystals of weakly pinned superconductors CeRu2 and 2H-NbS2. 2H-NbS2 is iso-structural and iso-electronic to 2H-NbSe2, whose similarity with CeRu2 as regards the PE representing the order-to-disorder transformation of the flux line lattice was claimed some time ago. We
report on the step change in equilibrium magnetization across the peak effect in CeRu2. We also present the vortex phase diagram of 2H-NbS2 obtained from the magnetization data, and compare the PE phenomenon in 2H-NbS2 and 2H-NbSe2. 相似文献
32.
Ghesquière J Gauthier N De Winter J Gerbaux P Moucheron C Defrancq E Kirsch-De Mesmaeker A 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(1):355-364
Ru(II)-TAP complexes have been shown to be very attractive compounds in the frame of developments of new anticancer drugs targeting the genetic material. This increasing interest originates from observations of covalent bond formations, triggered by photo-induced electron transfer (PET) between Ru(II)-TAP complexes and guanine bases of DNA. This photoreaction has recently been extended to the tryptophan (Trp) amino acid for future applications involving peptides. Thus, a double photo-addition of Trp residues of peptides on Ru(II) complexes is demonstrated by mass spectrometry with some structural issues. Such bi-adduct formations offer the possibility of photocrosslinking two Trp-containing biomolecules, which is investigated in this study. Thus, photocrosslinking between two complementary oligonucleotides (ODNs) derivatized by Trp-containing tripeptides is demonstrated by polyacrylamide gel electrophoresis (PAGE) in the presence of Ru(II)-TAP complexes. Both PAGE and MS indicate that such photocrosslinkings arise from two reaction pathways: either via the double addition of Trp residues on the Ru complex or from dimerization of Trp radicals. The competition between these two pathways depends on the experimental conditions. Heterobridgings between guanine bases and tryptophan residues mediated by Ru(II)-TAP complexes is also examined, opening the way to ODN-peptide photocrosslinkings. 相似文献
33.
Vanderlinden W Blunt M David CC Moucheron C Kirsch-De Mesmaeker A De Feyter S 《Journal of the American Chemical Society》2012,134(24):10214-10221
We used scanning force microscopy (SFM) to study the binding and excited state reactions of the intercalating photoreagent Ru[(TAP)(2)PHEHAT](2+) (TAP = 1,4,5,8-tetraazaphenanthrene; PHEHAT = 1,10-phenanthrolino[5,6-b]1,4,5,8,9,12-hexaazatriphenylene) with DNA. In the ground state, this ruthenium complex combines a strong intercalative binding mode via the PHEHAT ligand, with TAP-mediated hydrogen bonding capabilities. After visible irradiation, SFM imaging of the photoproducts revealed both the structural implications of photocleavages and photoadduct formation. It is found that the rate of photocleaving is strongly increased when the complex can interact with DNA via hydrogen bonding. We demonstrated that the photoadduct increases DNA rigidity, and that the photo-biadduct can crosslink two separate DNA segments in supercoiled DNA. These mechanical and topological effects might have important implications in future therapeutic applications of this type of compounds. 相似文献
34.
Amandine Kolleth Dylan Dagoneau Pierre Quinodoz Alexandre Lumbroso Mickael Avanthay Saron Catak Sarah Sulzer‐Moss Alain De Mesmaeker 《Helvetica chimica acta》2019,102(9)
Herein, we describe a very straightforward and metal free method for the synthesis of benzazepinones through an intramolecular cyclization. This involves an ortho‐vinyl‐anilino‐amide as starting material which is converted to a keteniminium intermediate that spontaneously cyclize to form a 7‐membered ring iminium. Under slightly basic hydrolysis conditions, this latter is ultimately converted to the desired benzazepinone. Control experiments on the electron density of the nitrogen constituting the aniline were performed to support our proposed mechanism and rationalize the selectivity of the reaction. 相似文献
35.
Jean-Paul Lecomte Andrée Kirsch -De Mesmaeker John M. Kelly Alex B. Tossi Helmut Görner 《Photochemistry and photobiology》1992,55(5):681-689
The luminescence quenching of ruthenium-tris-1,4,5,8-tetraazaphenanthrene [Ru(tap)3(2+)] by nucleotides approaches the diffusion rate only with guanosine-5'-monophosphate (GMP), the most reducing nucleotide, and leads to an electron transfer with the production of the monoreduced complex and the oxidized base. The resulting deprotonated GMP(-H).radical recombines with the monoreduced complex according to a bimolecular equimolar process. The pH dependence of the decay of the transient reduced complex, in the presence of an oxidant (oxygen or benzoquinone) indicates the formation of Ru(tap)2(tapH)2+, i.e. the reduced protonated species, subsequent to the electron transfer, with a pKa of 7.6 as confirmed from pulse radiolysis experiments. As the non-protonated reduced complex, Ru(tap)2(tap-.)+, has a higher reducing power than the protonated one, oxygen is able to reoxidize only the non-protonated species, whereas benzoquinone reoxidizes both species but with different rate constants. The flash photolysis of Ru(tap)3(2+) in the presence of DNA and the effect of Mg2+ ions and GMP as supplementary additives also show the existence of a photo-induced electron transfer with the nucleic acid, which can be correlated to the photosensitized cleavage of DNA by this complex. 相似文献
36.
Latterini L Pourtois G Moucheron C Lazzaroni R Bredas JL Kirsch-De Mesmaeker A De Schryver FC 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(8):1331-1336
Scanning tunneling microscopy (STM) and molecular mechanics calculations were used to investigate the long-range packing and the structure of an heptanuclear ruthenium (II) dendritic species, as a PF6- salt. STM imaging was carried out on a mono-add layer of the ruthenium dendrimer formed by physisorption from a 1,2,4-trichlorobenzene solution at the liquid-graphite interface. The packing of the molecules on the surface was visualised by the formation of ordered patterns and a distance of 27 +/- 2 A was measured between two adjacent lamellae. The comparison of this dimension with the molecular-modelling data indicates that the lamellae were formed by rows of dendrimer molecules in which the counterions (PF6-) were strongly associated with the Ru atoms. The images acquired with higher spatial resolution revealed the presence of repeating units within the lamellae. The comparison of the STM images with the modelling results allowed the attribution of the repeating units observed in the imaged pattern to the STM signature of single dendrimer molecules. 相似文献
37.
Mathilde Lachia François Richard Raphael Bigler Amandine Kolleth-Krieger Michael Dieckmann Alexandre Lumbroso Ulfet Karadeniz Saron Catak Alain De Mesmaeker 《Tetrahedron letters》2018,59(20):1896-1901
γ-Lactams are important building blocks for the synthesis of biologically active molecules and can easily be accessed via Beckmann rearrangement of cyclobutanones. However, Beckmann fragmentation is often a competing reaction for these strained ketones. We found that performing the Beckmann rearrangement with Tamura’s reagent in the presence of aqueous HCl suppresses the undesired fragmentation reaction. This improved procedure was applied to a broad scope of substrates affording monocyclic, bicyclic, tricyclic or spirocyclic lactams.Our experimental results and DFT calculations suggest that the mechanism of the rearrangement probably involves a tetrahedral intermediate and doesn’t proceed via oxime fragmentation as in a classical Beckmann rearrangement. 相似文献
38.
Amandine Kolleth Simona Müller Alexandre Lumbroso Gamze Tanriver Saron Catak Sarah Sulzer-Mossé Alain De Mesmaeker 《Tetrahedron letters》2018,59(34):3242-3248
We described a general approach to 3-aminobenzothiophenes and 3-aminothiophenes fused to 5-membered heteroaromatic rings as thiophenes, furans and pyrroles through a 6π-elctrocyclization reaction of keteniminium salts. We investigated various substituents not only on the aromatic rings, but also at C-2 and on the nitrogen atom of the keteniminium salt. In particular, we have determined the electronic requirements of the nitrogen substitution to secure the efficient formation of the corresponding keteniminium salt. A clear relation between the pKa of the amine leading to the formation of the keteniminium salt and the yield obtained for benzothiophene is established and should find broad application to other reactions involving these intermediates. Additional insight on the ease of this 6π-electrocyclization reaction was gained through competition reactions and DFT calculations. 相似文献
39.
40.
We examine using Monte Carlo simulations, photon transport in optically ‘thin’ slabs whose thickness L is only a few times the transport mean free path l*, with particles of different scattering anisotropies. The confined geometry causes an auto-selection of only photons with
looping paths to remain within the slab. The results of the Monte Carlo simulations are borne out by our analytical treatment
that incorporates directional persistence by the use of the Ornstein-Uhlenbeck process, which interpolates between the short
time ballistic and long time diffusive regimes. 相似文献