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排序方式: 共有49条查询结果,搜索用时 15 毫秒
41.
42.
Sechi M Azzena U Delussu MP Dallocchio R Dessì A Cosseddu A Pala N Neamati N 《Molecules (Basel, Switzerland)》2008,13(10):2442-2461
HIV-1 integrase (IN) is an attractive and validated target for the development of novel therapeutics against AIDS. In the search for new IN inhibitors, we designed and synthesized three series of bis-amide and hydrazide-containing derivatives of malonic acid. We performed a docking study to investigate the potential interactions of the title compounds with essential amino acids on the IN active site. 相似文献
43.
Martins F Hackens B Pala MG Ouisse T Sellier H Wallart X Bollaert S Cappy A Chevrier J Bayot V Huant S 《Physical review letters》2007,99(13):136807
Combining scanning gate microscopy (SGM) experiments and simulations, we demonstrate low temperature imaging of the electron probability density |Psi|(2)(x,y) in embedded mesoscopic quantum rings. The tip-induced conductance modulations share the same temperature dependence as the Aharonov-Bohm effect, indicating that they originate from electron wave function interferences. Simulations of both |Psi|(2)(x,y) and SGM conductance maps reproduce the main experimental observations and link fringes in SGM images to |Psi|(2)(x,y). 相似文献
44.
Kaiser EW Donahue CJ Pala IR Wallington TJ Hurley MD 《The journal of physical chemistry. A》2007,111(7):1286-1299
The reactions of Cl atoms with cis- and trans-2-butene have been studied using FTIR and GC analyses. The rate constant of the reaction was measured using the relative rate technique. Rate constants for the cis and trans isomers are indistinguishable over the pressure range 10-900 Torr of N2 or air and agree well with previous measurements at 760 Torr. Product yields for the reaction of cis-2-butene with Cl in N2 at 700 Torr are meso-2,3-dichlorobutane (47%), DL-2,3-dichlorobutane (18%), 3-chloro-1-butene (13%), cis-1-chloro-2-butene (13%), trans-1-chloro-2-butene (2%), and trans-2-butene (8%). The yields of these products depend on the total pressure. For trans-2-butene, the product yields are as follows: meso-2,3-dichlorobutane (48%), dl-2,3-dichlorobutane (17%), 3-chloro-1-butene (12%), cis-1-chloro-2-butene (2%), trans-1-chloro-2-butene (16%), and cis-2-butene (2%). The products are formed via addition, addition-elimination from a chemically activated adduct, and abstraction reactions. These reactions form (1) the stabilized 3-chloro-2-butyl radical, (2) the chemically activated 3-chloro-2-butyl radical, and (3) the methylallyl radical. These radicals subsequently react with Cl2 to form the products via a proposed chemical mechanism, which is discussed herein. This is the first detailed study of stereochemical effects on the products of a gas-phase Cl+olefin reaction. FTIR spectra (0.25 cm(-1) resolution) of meso- and DL-2,3-dichlorobutane are presented. The relative rate technique was used (at 900 Torr and 297 K) to measure: k(Cl + 3-chloro-1-butene) = (2.1 +/- 0.4) x 10(-10), k(Cl + 1-chloro-2-butene) = (2.2 +/- 0.4) x 10(-10), and k(Cl + 2,3-dichlorobutane) = (1.1 +/- 0.2) x 10(-11) cm3 molecule(-1) s(-1). 相似文献
45.
Stable suspensions of small metal Au, Ru, PI, Pd, Rh, Co and Nl particles dispersed in n-heptane and n-dodecane have been prepared using a novel two-phase system, Involving the formation of the particles In a methanolic phase and subsequent phase transfer of the panicles to the alkane medium. The dispersions consisted of small particles having diameters In the range of 8-30 nm (the gold sols were very polydlsperse having average diameters of ca.34 nm). The phase transfer of the particles and their subsequent colloid stability were effected by the presence of dissolved dispersant in the hydrocarbon phase (either Oloa 1200 or Hypermer LP 8). In the case of Oloa 1200, a widely-used polylsobutylene succinimide automotive engine dispersant, It Is proposed that the amlne groups adsorb strongly to the acidic surface o1 the particles, and the 70-carbon polyisobutylene chains extend Into the hydrocarbon medium sufficiently to maintain the separation of adjacent particles by steric and possibly also by electrical repulsion. 相似文献
46.
N.Saidin D.I.M.Zen S.S.A.Damanhuri S.W.Harun H.Ahmad F.Ahmad K.Dimyati A.Halder M.C.Paul M.Pal S.K.Bhadra 《中国光学快报(英文版)》2013,(6):81-83
We report a ring cavity passively harmonic mode-locked fiber laser using a newly developed thuliumbismuth co-doped fiber(TBF) as a gain medium in conjunction with a carbon nanotube(CNT)-based saturable absorber.The TBF laser generates a third harmonic mode-locked soliton pulse train with a high repetition rate of 50 MHz and a pulse duration of 1.86 ps.The laser operates at 1 901.6 nm with an average power of 6.6 mW,corresponding to a pulse energy of 0.132 nJ,at a 1 552 nm pump power of 723.3 mW. 相似文献
47.
Triki S Bérézovsky F Sala Pala J Gómez-García CJ Coronado E Costuas K Halet JF 《Inorganic chemistry》2001,40(20):5127-5132
Electrochemical combination of the magnetic dinuclear anion [MM'(C2O4)(NCS)8](4-) (MM' = Cr(III)Cr(III), Cr(III)Fe(III)) with the ET organic pi-donor (ET = BEDT-TTF = bis(ethylenedithio)tetrathiafulvalene) gives rise to two new isostructural molecular hybrid salts ET5[MM'(C2O4)(NCS)8], with MM' = CrCr (1), CrFe (2). The molecular structure of compound 1 has been determined by single crystal X-ray diffraction. The particular arrangement of the organic units consists of an unprecedented two-dimensional organic sublattice nearly similar to that observed in kappa-phase structures. For both compounds, the magnetic susceptibility measurements indicate (i) the ET radicals do not contribute to the magnetic moment probably due to the presence of strong antiferromagnetic interaction between them, and (ii) in the anion, the magnetic coupling is antiferromagnetic for 1 (J = -3.65 cm(-1)) and ferromagnetic for 2 (J = 1.14 cm(-1), J being the parameter of the exchange Hamiltonian H = -2JS1S2). The field dependence of the magnetization of compound 2 at 2.0 K gives further evidence of the S = 4 ground-state arising from the interaction between S = 3/2 Cr(III) and S = 5/2 Fe(III). EPR measurements confirm the nature of the magnetic interactions and the absence of any contribution from the organic part, as observed from the static magnetic measurement. Conductivity measurements and electronic band structure calculations show that both salts are semiconductors with low activation energies. 相似文献
48.
Aragoni MC Arca M Devillanova FA Isaia F Lippolis V Mancini A Pala L Slawin AM Woollins JD 《Chemical communications (Cambridge, England)》2003,(17):2226-2227
The reaction of the neutral dithiolene [Pd(Et2timdt)2] (Et2timdt = formally monoreduced diethylimidazolidine-2,4,5-trithione) with an excess of Br2 yielded few crystals of [1(Et) x 2Br](2+)(Br-)2(Br2)3 as a by-product (1(Et) = 4,5,9,10-tetrathiocino-[1,2-b:5,6-b']-1,3,6,8-tetraethyl-diimidazolyl-2,7-dithione); X-ray diffraction analysis showed that this compound represents the first example of a polybromide 2D-network templated by [1(Et) x 2Br](+2) dications, and featuring all the Br-Br distances shorter than those found in solid state bromine. 相似文献
49.
We introduce the concept of "critical epinucleation to distinguish nucleation on surfaces with and without reconstruction. On a reconstructed surface, the critical classical nucleus is stable against dissociation, but may not yet break the underlying surface reconstruction. Consequently, there must exist a "critical epinucleus" that is not only stable but also has established the epiconfiguration by unreconstructing the underlying substrate. We illustrate this concept by first-principle calculation of homonucleation on reconstructed Si(001) surface where the critical epinucleus consists of six adatoms. 相似文献