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851.
Hydrated nitrosonium ion clusters NO(+)(H(2)O)(n) (n = 4 and 5) were investigated by using MP2/aug-cc-pVTZ level of theory to clarify isomeric reaction pathways for formation of HONO and fully hydrated hydride ions. We found some new isomers and transition state structures in each hydration number, whose lowest activation energies of the intracluster reactions were found to be 4.1 and 3.4 kcal mol(-1) for n = 4 and n = 5, respectively. These thermodynamic properties and full quantum mechanical molecular dynamics simulation suggest that product isomers with HONO and fully hydrated hydride ions can be obtained at n = 4 and n = 5 in terms of excess hydration binding energies which can overcome these activation barriers. 相似文献
852.
Abstract Seed dispersion polymerization of methyl methacrylate (MMA) in the presence of monodisperse PMMA particles was carried out in an aqueous methanol using poly(methacrylic acid) stabilizer. The polymerization using 2. 5 μ. m-sized seed particles gave monodisperse PMMA particles in the diameter up to 4. 9 μm. The solvent composition and monomer concentration greatly affected the polymerization behavior. Under appropriate conditions, monodisperse PMMA particles in the diameter up to 8. 9 μ, m was prepared from 4. 6 μm-sized seed particles. The seed dispersion polymerization of styrene in the presence of the seed particles produced monodisperse PMMA-polystyrene particles in the micron range. The particles were supposed to have a structure consisting of PMMA-core and polystyrene-shell from ESCA analysis. 相似文献
853.
Shun-ichi Hashimoto Hiroki Sakamoto Takeshi Honda Hiroshi Abe Sei-ichi Nakamura Shiro Ikegami 《Tetrahedron letters》1997,38(52):8969-8972
A stereocontrolled synthesis of globotriaosylceramide with three different glycosidic linkages has been accomplished by linear and convergent routes exploiting “armed-disarmed” glycosidation methodology based on glycosyl donors and acceptors carrying tetramethylphosphoroamidate as a leaving group. In particular, the convergent strategy featuring a coupling of a galactosyl-(1→4)-galactosyl donor with a glucosylceramide derivative has proven to be extremely efficient. 相似文献
854.
The recent progress on the light-emitting devices on Si substrate is reviewed. It is shown, in GaAs on Si, that the reduction of the thermal stress is essential to improve laser lifetime and also to decrease dislocation density. Several methods of reducing the thermal stress, such as the low temperature growth, three layer structure, and the post-growth patterning, are explained. In contrast to the GaAs system, the devices made of indium-related compounds such as InGaAs and InGaAsP are less sensitive to the dislocation and, hence, have superior laser lifetime compared to GaAs devices. The material aspects regarding the light emitters on Si are discussed. 相似文献
855.
Shiro Kubuki Hitomi Masuda Kazuhiko Akiyama Zoltán Homonnay Ernő Kuzmann Tetsuaki Nishida 《Hyperfine Interactions》2013,219(1-3):141-145
A relationship between electrical conductivity (σ) and local structure of 15Li2O·10Fe2O3·xSnO2·(70–x)V2O5·5P2O5 glass (x = 0–20 mol%), abbreviated as xLFSVP glass, was investigated by 57Fe- and 119Sn-Mössbauer spectroscopies, differential thermal analysis (DTA) and dc-four probe method. A small increase in quadrupole splitting (Δ) for FeIII was observed from 0.70 to 0.74± 0.02 mm s???1 with an increase of “x”, whereas isomer shift (Δ) values of 0.40±0.01 mm s???1 were independent of “x”. This result suggests that local distortion of FeIIIO4 tetrahedra was slightly increased in SnO2-containing vanadate glasses, which was reflected as an increase in glass transition temperature (Tg) from 266 to 285±5 °C. A slope of 675 K / (mm s???1) obtained in ‘Tg vs. Δ plot’ proved that FeIII occupied the site of network former (NWF). An isothermal annealing of 10LFSVP glass at 500 °C for 100 min resulted in a marked decrease of Δ from 0.72 to 0.56±0.02 mm s???1, indicating that local distortion of FeO4 tetrahedra was reduced by the structural relaxation of 3D-network. In contrast, identical δ and Δ values of 0.07±0.01 and 0.53±0.02 mms???1, respectively, were observed in 119Sn-Mössbauer spectra of 10LFSVP glass before and after the annealing. These results indicate that SnIVO6 octahedra are loosely bound in the glass matrix as a network modifier (NWM). A marked increase in σ from 7.4 × 10???7 to 9.1 × 10???3 S cm???1 was observed in 20LFSVP glass after the isothermal annealing, indicating that structural relaxation of 3D-network evidently causes a marked increase in σ. 相似文献
856.
Ryota Matsukawa Mina Yamane Prof. Motomu Kanai 《Chemical record (New York, N.Y.)》2023,23(11):e202300198
Histidine photooxygenation has been the subject of extensive investigation for many years. The intricate nature of histidine distinguishes it from other amino acids, as its side chain readily undergoes changes in charge state and tautomerization in response to pH, and the polarity of the imidazole ring inverts upon oxidation. This complexity gives rise to a diverse range of oxidation products and mechanisms, posing challenges in their interpretation. This review aims to provide a thorough overview of the chemistry involved in histidine photooxygenation, encompassing a comprehensive analysis of resulting products, mechanisms engaged in their formation, and analytical techniques that have contributed to their identification. Additionally, it explores a wide range of applications stemming from this transformation, offering valuable insights into its practical implications in fields such as materials science, biomedical research, and drug development. By bridging the existing gap in literature, this review serves as a resource for understanding the intricacies of histidine photooxygenation and its diverse ramifications. 相似文献
857.
Park YD Kim HK Kim JJ Cho SD Kim SK Shiro M Yoon YJ 《The Journal of organic chemistry》2003,68(23):9113-9115
N-Nitration of 4-chloro-5-substituted-pyridazin-3-one with copper nitrate trihydrate in acetic anhydride gave the corresponding 4-chloro-2-nitro-5-substituted-pyridazin-3-one. 4-Chloro-5-alkoxy-2-nitropyridazin-3-ones such as 5-methoxy (2b) and 5-ethoxy (2d) derivatives showed excellent nitro group transfer potentiality. N-Nitration of some secondary amines with 2b gave the corresponding N-nitramines under mild neutral condition in good yields. 相似文献
858.
Hiroshi Uyama Yoichiro Honda Shiro Kobayashi 《Journal of polymer science. Part A, Polymer chemistry》1993,31(1):123-128
The present article describes the synthesis and emulsion copolymerization of a block-type amphiphilic poly(2-oxazoline) macromonomer possessing a polymerizable vinyl ester group. The macromonomer was synthesized by one-pot two-stage block copolymerization of 2-oxazolines using vinyl iodoacetate as initiator. 2-Methyl- and 2-n-butyl-2-oxazolines were employed for the construction of hydrophilic and hydrophobic segments, respectively. The surface activities evaluated by the surface tension of the macromonomer in water were fairly good. Emulsion copolymerization of vinyl acetate with the macromonomer was carried out. The macromonomer acted as a polymeric surfactant, as well as a comonomer. The resulting copolymer latex particles were spherical and their diameter was in the sub-micron range. The effects of the composition of the macromonomer on the emulsion copolymerization and the resulting latex particles were examined. © 1993 John Wiley & Sons, Inc. 相似文献
859.
(±)-7-Deoxy-4-demethoxydaunomycinone((±)-3) was found to be cleanly resolved by forming a mixture of the diastereomereic acetals((-)-9and(+)-10 or(+)-9 and(-)-10)with the title vicinal-diol(+)-or ( )-5), affording optically pure (R)-( )-3. The resolving agents (( + )- and ( )-5) were readily synthesized from unnatural(2S,3S)-(-)-tartaric acid((-)-6)or D-(-)-mannitol and natural (2R,3R)-(+)-tartaric acid((+)6), respectively. The undesired enantiomer ((S)-(+ )-3) obtained by the optical resolution could be racemized by heating with trifluoromethanesulfonic acid in aq acetic acid. Optically pure (R)-3 was elaborated to optically pure (+)-4-demethoxydaunomycinone ((+)-2b) and (+)-demethoxyadriamycinone ((+)-2a) by featuring highly stereoselective ( ? 20:1) introduction of the OH group into the C7-position as a key step. 相似文献
860.
Kojima S Sugino M Matsukawa S Nakamoto M Akiba KY 《Journal of the American Chemical Society》2002,124(26):7674-7675
An anti-apicophilic phosphorane bearing an oxaphosphetane ring, in which the ring carbon is apical and the ring oxygen is equatorial (C-apical), has been prepared as a thermally less stable stereoisomer of a phosphorane with an ordinary equatorial carbon-apical oxygen array in the oxaphosphetane ring (O-apical). This novel C-apical phosphorane, which could be considered to be a model compound of the reactive intermediate in the Wittig reaction, was fully characterized by NMR and X-ray structural analysis. The compound was found to easily isomerize to its more stable O-apical isomer, especially in the presence of proton sources, and the latter O-apical compound was found to furnish olefin at elevated temperatures. 相似文献