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31.
Yoshiro Masuyama Kazuki YoshikawaNoriyuki Suzuki Kenji HaraAtsushi Fukuoka 《Tetrahedron letters》2011,52(51):6916-6918
Copper(II)-exchanged hydroxyapatite, prepared by ion-exchanging of Ca(II) in calcium hydroxyapatite [Ca10(PO4)6(OH)2] with Cu(NO3)2 at 70 °C in water, functions as a reusable heterogeneous catalyst with neither reducing agents nor bases for azide-alkyne [3+2] cycloaddition at 50 °C in water under air. 相似文献
32.
A remarkable effect of ionic liquids in transition-metal-free aerobic oxidation of benzylic alcohols
Yoshiro OdaKoji Hirano Tetsuya SatohSusumu Kuwabata Masahiro Miura 《Tetrahedron letters》2011,52(41):5392-5394
The transition-metal-free aerobic oxidation of benzylic alcohols is uniquely accelerated by a 1-butyl-3-methylimidazolium hexafluorophosphate (BMI-PF6)/PhCF3 biphasic system and Cs2CO3 to afford the corresponding ketones in good yields. The reaction system is also applicable to an oxidative cross-esterification of primary benzyl alcohols with a higher aliphatic alcohol. 相似文献
33.
The rotational time correlation function (RTCF) of solute benzene molecules in the ionic liquid (1-butyl-3-methylimidazolium chloride) has been studied using classical molecular dynamics simulation. The effect of solvent charge on the functional form of RTCF was investigated by comparing four force fields for the solvent where the total charge on the anion and the cation was set to ±1e, ±0.7e, ±0.5e, and 0, respectively. For all three charged solvent models, the RTCF exhibits a long-time tail where the relaxation rate exhibits a significant slowdown. This feature is strengthened by higher solvent charges as well as lower temperatures, indicating the influence of the strong Coulombic fields arising from the solvent charges. The long-time tail is caused by the extraordinarily slow solvent structural relaxation of ionic liquids compared to the time scale of their local vibrational and librational dynamics. 相似文献
34.
Room temperature ionic liquids (IL) have been used in numerous applications in chemistry. Addition of water alters many of their properties making it possible to custom design solvents for specific applications. Along with experiments, computational studies using various approaches have provided key insights into the structure and dynamics of IL systems, as well as aggregate formation and phase behavior of the IL/water mixtures. These systems provide computational challenges since ILs and IL/water mixtures are viscous liquids with intrinsically slow processes and structural organization over surprisingly large length scales, which push the limits of applicability of the available techniques. Recent developments in the studies of IL/water mixtures using computational methodologies are reviewed and the future prospects for the field are briefly discussed. 相似文献
35.
Imura Y Tanuma H Sugimoto H Ito R Hojo S Endo H Morita C Kawai T 《Chemical communications (Cambridge, England)》2011,47(22):6380-6382
Straight ultrathin Au nanowires (NWs) with diameters less than 2 nm were synthesized using the lamellar structure of C18AA in an organogel and its selective adsorption for specific gold surfaces. In addition, the potential to form a bilayer structure with interdigitated hydrocarbon chains enabled the production of water-dispersible Au NWs without morphological change. 相似文献
36.
Kosumi D Kusumoto T Fujii R Sugisaki M Iinuma Y Oka N Takaesu Y Taira T Iha M Frank HA Hashimoto H 《Physical chemistry chemical physics : PCCP》2011,13(22):10762-10770
Carotenoids containing a carbonyl group in conjugation with their polyene backbone are naturally-occurring pigments in marine organisms and are essential to the photosynthetic light-harvesting function in aquatic algae. These carotenoids exhibit spectral characteristics attributed to an intramolecular charge transfer (ICT) state that arise in polar solvents due to the presence of the carbonyl group. Here, we report the spectroscopic properties of the carbonyl carotenoid fucoxanthin in polar (methanol) and nonpolar (cyclohexane) solvents studied by steady-state absorption and femtosecond pump-probe measurements. Transient absorption associated with the optically forbidden S(1) (2(1)A) state and/or the ICT state were observed following one-photon excitation to the optically allowed S(2) (1(1)B) state in methanol. The transient absorption measurements carried out in methanol showed that the ratio of the ICT-to-S(1) state formation increased with decreasing excitation energy. We also showed that the ICT character was clearly visible in the steady-state absorption in methanol based on a Franck-Condon analysis. The results suggest that two spectroscopic forms of fucoxanthin, blue and red, exist in the polar environment. 相似文献
37.
Khai Xuan Pham Rie Tanabe Yoshiro Ito 《Applied Physics A: Materials Science & Processing》2013,112(2):485-493
Laser-induced periodic surface structures (LIPSSs) were observed on the sidewalls of 300-μm-diameter holes trepanned on cemented tungsten carbide using femtosecond laser pulses at a wavelength of 800 nm. For a circularly polarized beam, LIPSSs were formed at a period of 300 nm and oriented perpendicularly to the plane of incidence on the sidewalls. For a linearly polarized beam, LIPSS formation was dependent on the relative angle α between the polarization direction and the plane of incidence. For relative angles α from 0° to 70° and from 110° to 180°, LIPSS spacing was 300 nm. However, there were two types of LIPSSs coexisting from 70° to 110°. One had a spacing of 120 nm and the other had a spacing that varied from 500 to 760 nm. It was found that the orientation angle of LIPSSs measured between the LIPSS orientation and the plane of incidence had a nonlinear dependence on α. To understand this dependence, a model was proposed in which LIPSSs are assumed to align perpendicularly to the direction of the absorbed electric field lying in the tangent plane of the sidewall of a drilled hole. The calculated results from this model showed good agreement with the experimental results. 相似文献
38.
Bungo Ochiai Jun‐ichi Nakayama Masayuki Mashiko Yoshiro Kaneko Tomomi Nagasawa Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2005,43(23):5899-5905
This article describes the polyaddition of bifunctional five‐membered cyclic carbonates and diethylenetriamine. The polyaddition proceeded via the selective addition of the primary amino group to the cyclic carbonates to give poly(hydroxyurethane)s bearing a secondary amine structure in the main chain. The resulting poly (hydroxyurethane) having a secondary amine structure was crosslinked by a reaction with a bifunctional dithiocarbonate to give a networked poly(hydroxyurethane–mercaptothiourethane). © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5899–5905, 2005 相似文献
39.
40.
Yoshiro Tatsu Soichiro Yamamura Hitoshi Yamamoto Susumu Yoshikawa 《Fresenius' Journal of Analytical Chemistry》1995,351(8):782-785
The fluorescence intensity of 5(6)-carboxyfluorescein (CF) was decreased by addition of horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The reaction inside a liposome containing CF and HRP on addition of H2O2 was measured fluorometrically after destruction of the liposome with Triton X-100. The reaction efficiency was higher than that without liposome because CF and HRP were concentrated inside the latter. The determination of H2O2 can be performed with a smaller amount of HRP by liposome encapsulation. 相似文献