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81.
Joo-Hyong Noh Shigehiko Hasegawa Tatsuya Suzuki Taro Arakawa Kunio Tada Hajime Asahi 《Physica E: Low-dimensional Systems and Nanostructures》2004,23(3-4):482
The five-layer asymmetric coupled quantum well (FACQW) is a new potential-tailored quantum well that is promising for ultra-fast and ultra-low-voltage optical modulators and switches. FACQW samples were grown by the migration-enhanced epitaxy (MEE) and the conventional molecular beam epitaxy methods with steep and flat heterointerfaces in the monolayer accuracy. They were characterized with the cross-sectional scanning tunneling microscopy (STM). In the cross-sectional STM image, double-stripe structures with different contrast were observed. The stripe area corresponds to the FACQW (about 10 nm wide), sandwiched with the AlGaAs barrier layers (15 nm wide). A dark line observed at the middle of the FACQW stripe area corresponds to the 3-monolayer-thick AlAs layer. The cross-sectional STM images of the high-quality heterointerface FACQW structures were successfully observed for the samples grown by the MEE method. More detailed studies of this kind of cross-sectional STM observations will be very effective to obtain the optimized growth conditions for fine and complicated ultra-thin structures. 相似文献
82.
Lei Gao Koji Narita Taro Ozaki Naoyoshi Kumakura Pamela Gan Atsushi Minami Chengwei Liu Xiaoguang Lei Ken Shirasu Hideaki Oikawa 《Tetrahedron letters》2018,59(12):1136-1139
Two homologous gene clusters for the biosynthesis of sesterterpenes betaestacins were identified from two phytopathogens, Phoma betae and Colletotrichum orbiculare. Heterologous expression of identified oxidation enzymes with previously-characterized PbTS1 (BtcAPb) resulted in the production of seven novel sesterterpenes. Although both strains possessed homologous enzymes, oxidation state of corresponding products were different from each other, suggesting that structural diversification of sesterterpene skeletons might be achieved by these homologous enzymes with different functions. 相似文献
83.
Taro Asuke 《Transactions of the American Mathematical Society》1996,348(5):1939-1958
Transversely flat conformal foliations with good transverse invariant measures are Riemannian in the sense. In particular, transversely similar foliations with good measures are transversely Riemannian as transversely -foliations.
84.
[Pt(0)(binap)(2)] (binap = 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl) is found to exhibit a luminescence from metal-to-ligand charge transfer state (MLCT) with a quantum yield of 0.12 and a lifetime of 1.2 micros in toluene at an ambient temperature. Prompt fluorescence with a quantum yield of 1.6 x 10(-)(4) is observed by means of a picosecond time-correlated single photon counting technique. The spectrum of the steady-state luminescence is almost identical to that of the prompt fluorescence, indicating that the intense luminescence is mainly delayed fluorescence from thermally activated (1)MLCT. The analysis of the temperature-dependent emission indicates that the energy difference between the (1)MLCT and (3)MLCT is 1.15 x 10(3) cm(-)(1). The lifetime of the prompt fluorescence is determined to be 3.2 ps from the decay of stimulated emission overlapped on subpicosecond transient absorption spectra. The lifetime of the (1)MLCT is much longer than expected from the large spin-orbit coupling constant of 5d (Pt) electrons (4000 cm(-)(1)). Theoretical analysis based on density functional theory reveals that structural distortion in the MLCT states causes large energy splitting between HOMO and HOMO - 1, which prevents a very fast ISC induced by strong spin-orbit interactions between these orbitals. The relatively slow ISC is therefore induced by weak spin-orbit interactions (ca. 50 cm(-)(1)) between ligand-centered molecular orbitals. Theoretical calculations indicate that the phosphorescence observed at lower temperatures is due to intensity borrowing from 4(1)B(2) --> GS transition. However, the large energy difference between HOMO and HOMO - 2 reduces the extent of mixing between the lowest (3)MLCT and 4(1)B(2) due to spin-orbit interaction, thereby decreasing the radiative rate of the phosphorescence. 相似文献
85.
The triangular six-electron cluster complex [Mo3S4Cl4(PEt3)
x
(thf)5] produced by the excision reaction of Mo3S7Cl4 with triethypholsphine is reduced by magnesium at – 20°C. Subsequent addition of dppe (=1,2-his(diphenylphosphino)ethane) to the reduced species affords a seven-electron triangular cluster complex [Mo3S4Cl3(dppe)2(PEt3)]. The complex crystallizes in the space groupCm witha=17.170(6),b-19.878(6),c = 13.289(5) = 121.73(2)°,V = 3858(2) A3, andZ = 2. The structure shows an almost equilateral triangle of three molybdenum atoms capped by a Sulfur atom and bridged by three sulfur atoms. The Mo Mo distances, ranging from 2.804(1) to 2.809(1) A are elongated ca. 0.04 A as compared with lose of a six-electron cluster complex with drape ligands. Two molybdenum atoms have a chlorine and a dppe ligands, and the other molybdenum atom bas a chlorine and a triethylphosphine ligands. The UV-Vis spectrum has a characteristic broad hand centered at 1410 n m, which is not observed for six-electron clusters. The ESR spectrum indicates the presence of an unpaired electron consistent with the formulation of the compound as a seven-electron cluster.Dedicated to Professor fiaxi Lu on the occasion of his 80th birthday. 相似文献
86.
The angular intensity distributions of CO and N(2) molecules scattered from a LiF(001) surface have been measured as functions of surface temperature, incident translational energy, and incident azimuthal direction affecting surface corrugation at a high resolution. Although both molecules have the same molecular mass and linear structure, only the CO molecule shows a rainbow feature in its scattering pattern, while the N(2) molecule shows a single peak distribution. From the comparisons of the obtained results with the calculated predictions based on the newly developed classical theory of the ellipsoid-washboard model, the differences in scattering distribution are attributed to the effects of molecular anisotropy and center-of-mass position. With an increase in the extent of the molecular anisotropy such as that of N(2) and CO as compared with rare-gas atoms, the summation of several scattering distributions depending on molecular orientation results in smearing the rainbow scattering on the corrugated surface. This smearing effect, however, attenuates when center-of-mass position deviates from the molecular center, as that for CO. 相似文献
87.
Saito T Sunaga T Sakai N Nakamura Y Yamamoto S Iriuchijima D Yoza K 《Inorganic chemistry》2005,44(12):4427-4432
A trinuclear rhenium sulfide cluster complex, [(Ph(3)P)(2)N][Re(3)(mu(3)-S)(mu-S)(3)Cl(6)(PMe(2)Ph)(3)], synthesized from Re(3)S(7)Cl(7), dimethylphenylphosphine, and [(Ph(3)P)(2)N]Cl is readily converted to a bridging SO(2) complex, [(Ph(3)P)(2)N][Re(3)(mu(3)-S)(mu-S)(2)(mu-SO(2))Cl(6)(PMe(2)Ph)(3)], by reaction with O(2). The oxygen atoms on the SO(2) ligand react with phosphines or phosphites to form phosphine oxides or phosphates, and the original cluster complex is recovered. The reaction course has been monitored by (31)P NMR as well as by UV-vis spectroscopy. The catalytic oxygenation of PMePh(2) in the presence of the SO(2) complex shows that turnovers are 8 per hour at 23 degrees C in CDCl(3). The X-ray structures of the cluster complexes are described. 相似文献
88.
Abstract— We have found that clay acts as a novel model matrix for the amphiphilic protein-opsin to mimic the visible absorption spectrum of a protonated retinal Schiff base (RSB) in vivo. Without strong acids at ambient temperature, a visible broad absorption spectrum with a LDmax at 530 nm covering the range from 400 to 680 nm was achieved for the protonated RSB with cationic surfactant-modified montmorillonite clay. The interlayers of the dimethyloctadecylamine (DOA) modified clay were found to provide amphiphilic space allowing the amphiphilic RSB to be intercalated easily and sequentially and protonated by the DOA. It is proposed that the visible absorption spectrum at LD, 530 nm was attributable to electrostatic effects, permitting the appropriate distance between the nitrogen of the protonated RSB and the negatively charged clay interlayers and also to the anisotropic orientation of the RSB molecules in the interlayers. 相似文献
89.
Summary A new method was developed for preparing an aqueous colloidal dispersion ofΒ-carotene. This method consists of preparing a solid mixture ofΒ-carotene and polyvinylpyrrolidone (PVP) from their chloroform solution by evaporating the solvent and dissolving the mixture
into water.
From filtration experiment and electron microscopic observation it was found thatΒ-carotene in its aqueous dispersion exists as colloidal particles with a diameter of about 100 ?. Spectroscopic data evidenced
thatΒ-carotene is molecularly dispersed in solid of PVP. It was considered that PVP acts as a solid solvent forΒ-carotene and, at the same time, a stabilizing agent for its aqueous dispersion. Instead of PVP, such a hydrophilic-oleophilic
substance as methylcellulose, polyvinylmethylether or Aerosol OT could be also used as the dispersing agent. Other materials
thanΒ-carotene could be dispersed by similar technique.
Zusammenfassung Es wird eine neue Methode zur Pr?paration einer w?\rigen Kolloid-Dispersion vonΒ-Carotin beschrieben. Diese Methode besteht aus Herstellen einer festen Mischung ausΒ-Carotin und Polyvinylpyrrolidon (PVP) aus der Chloroforml?sung durch Verdampfen des L?sungsmittels und anschlie\ende L?sung der Mischung in Wasser. Aus Filtration und elektronenmikroskopischen Aufnahmen l?\t sich zeigen, da\ dasΒ-Carotin molekulardispers im festen PVP verteilt ist. Das PVP wirkt offensichtlich als festes L?sungsmittel fürΒ-Carotin und gleichzeitig als stabilisiertes Agens für die w?\rige Dispersion. Anstelle von PVP k?nnen auch derartige hydrophile-oleophile Substanzen wie Methylcellulose, Polyvinylmethyl?ther oder Aerosol OT verwendet werden. Es k?nnen auch andere Materialien alsΒ-Carotin auf gleiche Weise dispergiert werden.相似文献
90.
Amagata T Amagata A Tenney K Valeriote FA Lobkovsky E Clardy J Crews P 《Organic letters》2003,5(23):4393-4396
[structure: see text] Structurally unique steroids, isocyclocitrinol A (1) and 22-acetylisocyclocitrinol A (2), were isolated from the extract of a saltwater culture of sponge-derived Penicilliun citrinum. The structures were established by analysis of 1D and 2D NMR data. The absolute structures were determined on the basis of X-ray structure analysis and application of modified Mosher's method. Furthermore, the structure of cyclocitrinol (3a) previously isolated from a terrestrial P. citrinum was revised as 3b. Compounds 1 and 2 showed weak antibacterial activity against Staphylococcus epidermidis and Enterococcus durans. 相似文献