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1.
We demonstrate the potential of femtosecond two-color pulse interferometry for in vitro optical glucose monitoring, by dispersion of the group refractive index in a glucose solution sample with respect to a red-color
light and a blue-color light. By comparison with femtosecond one-color pulse interferometry, the basic performance of the
present system with regard to sensitivity, quantitativeness, and tolerance to surrounding disturbances, is evaluated. The
resulting accuracy and precision of glucose determination are 77 and 118mg/dl for 10-mm-sample-thickness, respectively. This
near-common-path configuration of the two-color pulse light provides good stability to fluctuations of sample temperature,
which is important in clinical applications. Considering the performance of femtosecond two-color pulse interferometry as
an optical glucose sensor, a suitable measurement site for in vivo optical glucose monitoring is discussed. 相似文献
2.
3.
A wetting/dewetting process was utilized to prepare self-organized organic dye particles of micrometer and submicrometer size.
Near-field scanning optical microscopy successfully identified near-field excited near-field fluorescence from single particles.
The majority of the small particles with diameters around 2 mm or less, however, did not show fluorescence under near-field
observation. In contrast, far-field fluorescence, when excited by a polarized evanescent field, was observed, with the intensity
depending on the excitation polarization, indicating that molecules' transition moment within dye particles was oriented parallel
to the substrate surface. Single particle fluorescence spectrum consistently showed an identical sharp peak with a large redshift,
indicating that the particles were composed of identical dye aggregates similar to J-aggregates. These observations suggest
that the near-field at the probe tip was polarized parallel to the probe axis. Another observation, that molecules were oriented
in a similar direction among adjacent particles, suggests that the dewetting process contributed to the alignment of the molecular
direction among adjacent particles, which further proves that the present specimen was formed by a self-organizing mechanism. 相似文献
4.
Shindo M Yoshikawa T Itou Y Mori S Nishii T Shishido K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,12(2):524-536
Ynolates were found to react with alpha-alkoxy-, alpha-siloxy-, and alpha-aryloxyketones at room temperature to afford tetrasubstituted olefins with high Z selectivity. Since the geometrical selectivity was determined in the ring opening of the beta-lactone enolate intermediates, the torquoselectivity was controlled by the ethereal oxygen atoms. From experimental and theoretical studies, the high Z selectivity is induced by orbital and steric interactions rather than by chelation. In a similar manner, alpha-dialkylamino ketones provided olefins with excellent Z selectivity. These products can be easily converted into multisubstituted butenolides and gamma-butyrolactams in good yield. 相似文献
5.
Masahiko Ishikawa Ken-ichi Okamoto Jinsai Hidaka Hisahiko Einaga 《Helvetica chimica acta》1985,68(7):2015-2021
Substitution reaction with ethylenediamine of coordinated glycinate ligand in bis(ethylenediamine)-glycinatocobalt(III) complex has been studied in the presence of photo-excited tris(2,2′-bipyridine)ruthenium(II) complex in alkaline aqueous solution (buffered around pH 12) containing 1.0M chloride ion at 25°C. VIS absorption and CD spectra were used for the racemate and the optically active isomers of the Co(III) complexes, respectively. The reaction was catalyzed by the excited Ru(II) complex to give tris(ethylenediamine)cobalt(III) complex. Mechanism of the ligand-substitution reaction and role of the excited Ru(II) complex were discussed. 相似文献
6.
Preparation processes for Pt-deposited TiO(2) (Pt/TiO(2)) by the synthesis of Pt nanoparticles and their deposition were pursued by transmission electron microscopy, extended X-ray absorption fine structure, UV-vis spectroscopy, and Fourier transform infrared spectroscopic studies. Colloidal dispersions of Pt particles stabilized by poly(N-vinyl-2-pyrrolidone) (PVP) were photochemically synthesized in aqueous ethanol solution. The average diameter of Pt particles was estimated to be 2.0 +/- 0.5 nm, which was almost unchanged by changing the reducing agent from ethanol to methanol and 2-propanol. The PVP-stabilized Pt particles were distributed over a TiO(2) surface only by mixing the Pt colloidal dispersions and TiO(2). CO was chemically coordinated on the Pt particles on a TiO(2) surface after heat treatment was carried out in an O(2) flow at 673 K to completely remove the residual PVP on Pt/TiO(2). Hydrogen reduction at 473 K did not increase the amount of CO adsorbed on Pt sites. The Pt/TiO(2) catalyst after the oxidation treatment showed higher activity for CO photooxidation than that obtained for pure TiO(2) catalyst. The CO photooxidation rate was not unchanged by the H(2) reduction. 相似文献
7.
Summary Studies have been made on the distribution of iron(III)-ethyl acetoacetate complex between aqueous solution and benzene. Effect of pH, concentration of ethyl acetoacetate and shaking conditions were chosen as experimental parameters. Iron(III) can be well extracted from aqueous solution of pH 4.4–9.8 into benzene with constant extractability (97%), if the concentration of ethyl acetoacetate is kept in excess over that of iron(III). The applicability of the complex (
max: 452 nm) to the spectrophotometric determination of iron is also discussed.
Verteilung des Eisen(III)-Acetessigester-Komplexes zwischen wä\riger Lösung und Benzol
Zusammenfassung Zur Untersuchung der Verteilung wurden der pH-Wert, die Konzentration an Acetessigester und die Ausschüttelungsbedingungen variiert. Eisen(III) kann bei pH 4.4–9.8 mit Benzol mit einer konstanten Extrahierbarkeit von 97% ausgeschüttelt werden, wenn die Konzentration an Acetessigester größer ist als die an Eisen(III). Die Anwendbarkeit des Komplexes ( max: 452 nm) zur spektralphotometrischen Eisenbestimmung wird diskutiert.相似文献
8.
Size, shape, and flexibility of micelles of octaoxyethylene tetradecyl C(14)E(8), hexadecyl C(16)E(8), and octadecyl C(18)E(8) ethers in dilute aqueous solutions were determined at finite surfactant concentrations c by static light scattering (SLS) and dynamic light scattering experiments at several temperatures T below the critical points. The SLS results were successfully analyzed with the aid of the thermodynamic theory formulated with wormlike spherocylinder model for SLS of micelle solutions. The analysis yielded the molar mass M(w) of the micelles as a function of c and the cross-sectional diameter d. The hydrodynamic radius R(H) and the radius of gyration S(2)(1/2) of the micelles as functions of M(w) were found to be also well-described by the corresponding theories for the wormlike spherocylinder or wormlike chain models. The results of the stiffness parameter lambda(-1) have revealed that the micelles are far from rigid rods but rather stiff compared with typical flexible polymers and they grow in size with increasing T to greater length for longer hydrophobic chains, i.e., alkyl groups of the surfactants. As the alkyl group becomes longer, the d value increased, while the spacings s between adjacent hexaoxyethylene chains on the micellar surface were found to remain substantially constant. 相似文献
9.
Photoinduced magnetization of the cyano-bridged 3d-4f heterobimetallic assembly Nd(DMF)4(H2O)3(mu-CN)Fe(CN)5.H2O (1) (DMF = N,N-dimethylformamide) is described in this paper. The chiMT values are enhanced by about 45% after UV light illumination in the temperature range of 5-50 K. We propose that UV light illumination induces a structural distortion in 1. This small structural change is propagated by molecular interactions in the inorganic network. Furthermore, the cooperativity resulting from the molecular interaction functions to increase the activation energy of the relaxation processes, which makes observation of the photoexcited state possible. The flexible network structure through the hydrogen bonds in 1 plays an essential role for the photoinduced phenomenon. This finding may open up a new domain for developing the molecule-based magnetic materials. 相似文献
10.
Some N-alkyl-naphthylazo pyridinium salts as new reagents for the spectrophotometric determination of anionic surfactants 总被引:1,自引:0,他引:1
Summary Eleven pyridinium azo dyes with straight-chain alkyl groups CnH2n+1–(n=6–18) and bromoalkyl groups BrCmH2m–(m=6–12) were synthesized with the intention of developing reagents for the determination of low levels of anionic surfactants in an aqueous medium. The effect of the alkyl chain length of these reagents on the reactivity with anionic surfactants such as sodium dodecylsulphate (SDS), sodium linear-dodecylbenzenesulphonate (DBS), sodium dodecylsulphonate (DS) and sodium laurate (SL) was studied. It was found that the alkyl chain length played an important role in the formation of ion associates and the composition of the ion associates formed. These reagents were classified into four groups with respect to the reactivity with anionic surfactants. The first group (n,m=6) reacts only with DBS. The second group (n,m=8) reacts with SDS, DBS and DS. The third group (n,m=10, 12) reacts with SDS, DBS and DS; however, the colour intensity of the DBS-ion associate was unstable. The fourth group (n=14, 16, 18) reacts with all anionic surfactants examined, and the composition of the ion associates with SDS and DS was 2:1 ([reagent]/[surfactant]) though that of the ion associates of the three reagent groups mentioned above was 1:1. The optimal conditions for the determination of anionic surfactants in river water with 1-octyl-4-(4-aminonaphthylazo)-pyridinium bromide was examined. The calibration graph was linear up to 3×10–6 mol/l, and the apparent molar absorptivity of the ion associate was 3.8×104 l mol–1 cm–1 (at 427 nm). The relative standard deviation for 2.4×10–6 mol/l SDS was 4.9%. Recoveries of 88–107% were found for 8.0×10–7 mol/l SDS in river water samples. 相似文献