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951.
952.
Taotao Hao Yongsheng Yang Wenting Liang Chunying Fan Xin Wang Wanhua Wu Xiaochuan Chen Haiyan Fu Hua Chen Cheng Yang 《Chemical science》2021,12(7):2614
Stilbene derivatives have long been known to undergo “acid-catalyzed” Z → E isomerization, where a strong mineral acid at high concentration is practically necessary. Such severe reaction conditions often cause undesired by-reactions and limit their potential application. Herein, we present a trace mild acid-catalyzed Z → E isomerization found with stilbene derivatives fused with a norbornene moiety. By-reactions, such as the migration of the C C double bond and electrophilic addition reactions, were completely inhibited because of the ring strain caused by the fused norbornene component. Direct photolysis of the E isomers at selected wavelengths led to the E → Z photoisomerization of these stilbene derivatives and thus constituted a unique class of molecular switches orthogonally controllable by light and acid. The catalytic amount of acid could be readily removed, and the Z → E isomerization could be controlled by turning on/off the irradiation of a photoacid, which allowed repeated isomerization in a non-invasive manner. Moreover, the Z isomer produced by photoisomerization could spontaneously self-recover to the E isomer in the presence of a catalytic amount of acid. The kinetics of Z → E isomerization were adjustable by manipulating catalytic factors and, therefore, unprecedented molecular photoswitches with adjustable self-recovery were realized.Quantitative Z → E isomerization was catalyzed by trace mild acids to offer molecular switches orthogonally controllable by acid and light. 相似文献
953.
954.
In the presence of a silylating reagent and catalytic amount of Ni(acac)2, organozinc halides reacted with aromatic aldehydes to give the corresponding dialkylation products in good to excellent yields under mild conditions. 相似文献
955.
956.
957.
958.
Yali Fu Jingchang Zhang Zhong Huang Xiuyu Wang Yuguang Lv Weiliang Cao 《Journal of photochemistry and photobiology. A, Chemistry》2008,197(2-3):329-334
Four ternary complexes of Tb(III) were synthesized by introducing the first ligand (L1) (N-phenylanthranilic acid (N-HPA), α-furoic acid (FURA)) and the second ligand (L2) (1,10-phenanthroline (Phen), 2,2′-dipyridyl (Bipy)), respectively. These complexes were characterized by elemental analysis, infrared spectra, XRD, UV spectra and fluorescence spectra. The effect of L1 and L2 on the fluorescence properties of terbium complexes was discussed. It showed that all the complexes exhibited ligand-sensitized green emission. The fluorescent intensity increased in the sequence of Tb(FURA)3Bipy < Tb(N-PA)3Phen < Tb(FURA)3Phen < Tb(N-PA)3Bipy. It indicated that L1 affected fluorescence properties of the complexes differently when the corresponding L2 altered. Meanwhile, the influence of L2 on the luminescence properties of the complexes also depends on L1. The results showed that L1 and L2 affected each other and worked together as a whole. The matching of L1, L2 and Tb3+ ion is very important to the luminescence properties of Tb(III) ternary complexes. 相似文献
959.
Electron–hole recombination and photocorrosion are two challenges that seriously limit the application of two-dimensional (2D) transition metal dichalcogenides (TMDs) for photocatalytic water splitting. In this work, we propose a 2D van der Waals MoSe2/Ti2CO2 heterojunction that features promising resistance to both electron–hole recombination and photocorrosion existing in TMDs. By means of first-principles calculations, the MoSe2/Ti2CO2 heterojunction is demonstrated to be a direct Z-scheme photocatalyst for overall water splitting with MoSe2 and Ti2CO2 serving as photocatalysts for hydrogen and oxygen evolution reactions, respectively, which is beneficial to electron–hole separation. The ultrafast migration of photo-generated holes from MoSe2 to Ti2CO2 as well as the anti-photocorrosion ability of Ti2CO2 are responsible for photocatalytic stability. This heterojunction is experimentally reachable and exhibits a high solar-to-hydrogen efficiency of 12%. The strategy proposed here paves the way for developing 2D photocatalysts for water splitting with high performance and stability in experiments.The two challenges of electron–hole recombination and photocorrosion for two-dimensional transition metal dichalcogenides in the application of photocatalytic water splitting are simultaneously suppressed by rational design of heterojunctions. 相似文献
960.
The cyclic voltammetry, convolution voltammetry and chronopotentiometry were used to study the electrode process of Nd (III) reduced on iron electrode in molten NaCl-KCl-NdCl3 from 700 to 850°C. The electrodeposited products were analysed by X-ray diffraction. The results indicate that the intermetallic compound Fe2Nd forms first, and then the metallic neodymium deposits when Nd (III) is reduced on iron electrode. The Nd-Fe alloys rich in neodymium can be obtained by electrolysis with iron cathode in molten chlorides. The Nd-Fe alloys are composed of Fe2Nd and Nd. 相似文献