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131.
Synthesis of medium-sized carbocyclic ketones via the intramolecular B-alkyl Liebeskind-Srogl coupling reaction is described. The sequence of hydroboration of ω-alkenyl thiol ester with 9-BBN and the Liebeskind-Srogl reaction results in the formation of medium-sized carbocyclic ketones with good yield. 相似文献
132.
G. Z. Stasevich V. L. Stepanenko M. V. Kudrevatykh O. Yu. Avrutina O. N. Bubel 《Chemistry of Heterocyclic Compounds》2003,39(6):707-712
5-Hydroxy-3-(1-oxo-2,3-epoxyalkyl)benzofurans were obtained with yields of up to 81% by the reaction of p-benzoquinone with oxiranyl -dimethylaminovinyl ketones in acetic acid. 相似文献
133.
134.
Y. Paul Handa Zhiyi Zhang Jacques Roovers 《Journal of Polymer Science.Polymer Physics》2001,39(13):1505-1512
tert‐Butyl‐substituted poly(ether ether ketone) (tBuPEEK), which does not undergo crystallization with thermal annealing, crystallizes readily when treated with compressed CO2. The dissolved CO2 causes a reduction in the glass‐transition temperature of the polymer–gas system and enhances the chain mobility of the macromolecules, thereby bringing about crystallization. In the presence of CO2, crystallization is increasingly favored with increasing CO2 pressure and treatment temperature. The melting point of tBuPEEK crystals increases linearly with the CO2 pressure applied in the treatment, indicating an increase in the order and/or size of the crystals. The extent of crystallinity increases when small amounts of methanol or dichloromethane are used as a cosolute with CO2. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1505–1512, 2001 相似文献
135.
Li Hong Xiao Cheng Liu Xi Gao Jian 《中国化学快报》2008,19(2):227-229
A novel series of poly(aryl ether sulfone ketone)s (PPESKs) containing phthalazinone and biphenyl moieties were prepared by two-step nucleophilic polycondensation reaction. The ^-Mw values of these copolymers were between 38,330 and 67,900. The glass transition temperatures (Tg) and 5% decomposition temperatures were ranged in 253-269 ℃ and 488-500 ℃, respectively, The structures of these copolymers were confirmed by FT-IR and ^1H NMR. Moreover, all the resultant copolymers were amorphous determined by wide angle X-ray diffraction (WAXD). 相似文献
136.
A novel and efficient method of synthesis of 3-substituted derivatives of pentane-2,4-dione is proposed, wherein cheaper and
easily accessible chloro derivatives are conversed into more reactive iodo derivatives. The method is based on the Finkelstein
reaction for which the literature suggests highly polar organic solvents as ideal reaction media. In the presented work, the
use of industrially used ketones, especially methyl isobutyl ketone, is proposed. The use of MIBK as a solvent additionally
allows an azeotropic removal of water from the reaction mixture, enabling the application of moisture sensitive alkylating
agents i.e. (3-chloropropyl)trimethoxysilane. The obtained products are isolated through distillation, which does however
not allow the separation of C-alkylation products from O-alkylation ones. The products not containing water-sensitive substituents were isolated as copper complexes. The pure product
of C-alkylation was obtained by decomposition of the copper complex with a hydrochloric acid solution and extraction of the formed
ligand to an organic phase i.e. hexane. The obtained ligand can be further purified by distillation.
Presented at the 35th International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 26–30 May
2008. 相似文献
137.
Double Michael addition of nitromethane to divinyl ketones: A remarkably positive effect of additive
Yongqi Yao Yingying Liu Ling Ye Feng Chen Xinying Li Zhigang Zhao Xuefeng Li 《Tetrahedron》2017,73(16):2311-2315
An efficient double Michael addition of nitromethane to divinyl ketones was established in good to high yields (75–99%). A wide range of cyclohexanones were obtained with excellent diastereocontrol (up to >20:1 dr) and enantioinduction (91–99% ee) in a one-pot fashion. The involvement of basic additive significantly enhanced the reactivity of this cascade sequence. 相似文献
138.
Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones
<正>In this paper,a series of optically active MeO-BIPHEP-type ligands,(S)-6,6′-dimethoxy-2,2'-bis(di-p-alkoxyphenylphosphine)- 1,1′-biphenyl were synthesized and used to prepare the ruthenium complex.The effects of para-substituted were observed,the results showed that the ruthenium catalysts[diphosphine RuCl_2 diamine]containing both t-Bu and i-Pr substitutions have better activities and enantioselectivities than the non-substituted ruthenium catalysts in the asymmetric hydrogenation of acetophenone. 相似文献
139.
This paper reports on the preparation and characterization of sulfonated poly(ether ether ketone) (sPEEK)-based mixed matrix membranes. The inorganic matrix consisted of silica: Aerosil®380, tetraethoxysilane (TEOS) or a combination of both to obtain an interconnected silica network. The behavior of these membranes in ethanol–water systems was studied for application in a direct ethanol fuel cell (DEFC). Uptake measurements showed that the converted TEOS content had a strong influence on the hydrophilicity of the membranes. Proton conductivity was strongly related to the water content in the membrane, but the proton diffusion coefficients of membranes with various Aerosil®380–TEOS combinations were similar. Dynamic measurements in liquid–liquid (L–L) and liquid–gas (L–G) systems were performed to study the ethanol transport through the membrane. No reduction in ethanol permeability was obtained in the L–L system, but a remarkable reduction was obtained in the L–G system when 2 M ethanol was applied. The reinforcing characteristic of the combined Aerosil®380–TEOS-system were best observed at 40 °C with 4 M ethanol. The fuel cell performance prediction based on the selectivity of proton diffusion coefficient to ethanol permeability coefficient showed for nearly all composite membranes an improvement with respect to the polymeric reference. The presence of an inorganic phase led to relatively constant proton diffusion coefficients and lower ethanol permeability coefficients in comparison with the polymeric reference. 相似文献
140.
Laksmikanta Adak 《Tetrahedron letters》2010,51(29):3811-3814
Palladium(0) nanoparticles efficiently catalyze aliphatic aldehyde C-H functionalization by aryl halides to produce alkyl-aryl ketones in good yields. A wide range of substituted aryl and hetero-aryl bromides/iodides and open-chain aldehydes of varied chain length participated in this reaction. 相似文献