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931.
Xiao-Hui Li Li-He Lu Xu-Hong Li Yun-Biao Li Yuan-Chang Duan De-Huan Fu Shuang-Xi Mei Tao Cui Jing-Kun Wang Zhao-Yun Zhu 《Tetrahedron letters》2018,59(11):995-998
The extract of the aerial and underground parts of Phlomis likiangensis afforded two new iridoid derivatives, namely as phloloside H (1) and phloline (2), along with four known compounds (3–6), and compound 2 was a novel normonoterpene. Their structures were elucidated on the basis of spectroscopic studies and chemical methods. Six compounds were assayed for cytotoxic, antibacterial and antioxidative activities, but were either inactive or very weakly active. 相似文献
932.
Xue Li Kang Zhao Caiyin You Wensheng Linghu Feng Ye Mei Yu Ahmed Alsaedi Tasawar Hayat Hui Pan Jie Luo Xuemei Ren 《Journal of Radioanalytical and Nuclear Chemistry》2018,315(3):509-522
The characterization of the nanocomposites (PANI@GO) by SEM, TEM, Raman and FT-IR indicated that the GO has been functionalized via PANI successfully. PANI@GO as a novel platform for the removal of Cd(II), Eu(III), Th(IV) and U(VI) from aqueous solutions, the uptake process was a spontaneous endothermic process, and is strongly dependent of pH but independent of ionic strength. The adsorption kinetic and isotherm were fitted well the Pseudo-second-order equation and Langmuir model. PANI@GO were recycled and re-used without significant loss of adsorption capacity, and real samples were also treated which showed that had little interference with the performance of it. 相似文献
933.
Cover Feature: [CH3NH3]4Ga4SbS9S0.28O0.72H: A Three‐Dimensionally Open‐Framework Heterometallic Chalcogenidoantimonate Exhibiting Ni2+ Ion‐Exchange Property (Chem. Asian J. 6/2018) 下载免费PDF全文
Dr. Bo Zhang Wei‐An Li Yi‐Yu Liao Chen Zhang Dr. Mei‐Ling Feng Prof. Dr. Xiao‐Ying Huang 《化学:亚洲杂志》2018,13(6):585-585
934.
Chun Ma Jia‐Yu Zhou Yi‐Zhu Zhang Dr. Guang‐Jian Mei Prof. Dr. Feng Shi 《Angewandte Chemie (International ed. in English)》2018,57(19):5398-5402
The first catalytic asymmetric [2+3] cyclization of azlactones with azonaphthalenes has been established. This strategy allowed the synthesis of a variety of chiral isatin derivatives in generally good yields and excellent enantioselectivities (up to 99 % yield, 98 % ee). The developed reaction has not only established a catalytic enantioselective [2+3] cyclization using azlactones as two‐carbon building blocks, but also enriches the chemistry of catalytic asymmetric cyclizations of azonaphthalenes. In addition, this protocol will provide a useful method for constructing enantioenriched 3,3′‐disubstituted isatin‐type frameworks. 相似文献
935.
Nicolas Sauermann Dr. Ruhuai Mei Prof. Dr. Lutz Ackermann 《Angewandte Chemie (International ed. in English)》2018,57(18):5090-5094
Syntheses of substituted anilines primarily rely on palladium‐catalyzed coupling chemistry with prefunctionalized aryl electrophiles. While oxidative aminations have emerged as powerful alternatives, they largely produce undesired metal‐containing by‐products in stoichiometric quantities. In contrast, described herein is the unprecedented electrochemical C?H amination by cobalt‐catalyzed C?H activation. The environmentally benign electrocatalysis avoids stoichiometric metal oxidants, can be conducted under ambient air, and employs a biomass‐derived, renewable solvent for sustainable aminations in an atom‐ and step‐economical manner with H2 as the sole byproduct. 相似文献
936.
Yanbo Mei Dong‐Jun Wu Dr. Jaap E. Borger Prof. Dr. Hansjörg Grützmacher 《Angewandte Chemie (International ed. in English)》2018,57(19):5512-5515
A simple synthesis of sodium 2‐phosphanaphthalene‐3‐olate ( 1 ) based on the extrusion of N2 from phthalazine using Na[OCP] is reported. This heterocycle can be readily functionalized at the negatively charged oxygen center using a variety of electrophilic substrates. The coordination chemistry of both 1 and its neutral derivatives was explored, revealing their facile use as P‐donor ligands for late‐transition‐metal complexes. 相似文献
937.
Zong‐Jie Guan Jiu‐Lian Zeng Shang‐Fu Yuan Feng Hu Dr. Yu‐Mei Lin Prof. Quan‐Ming Wang 《Angewandte Chemie (International ed. in English)》2018,57(20):5703-5707
The controlled synthesis and structure determination of a bimetallic nanocluster Au57Ag53(C≡CPh)40Br12 (Au57Ag53) is presented. The metal core has a four‐shell Au2M3@Au34@Ag51 @Au20 (M=1/3 Au+2/3 Ag) architecture. In contrast to the previously reported large nanoclusters that have highly symmetric kernel structures, the metal atoms in Au57Ag53 are arranged in an irregular manner with C1 symmetry. This cluster exhibits excellent thermal stability and is robust under oxidative or basic conditions. The silver precursors play a key role in dictating the structures of the nanoclusters, which suggests the importance of the counteranions used. 相似文献
938.
Yingcai Wang Mei Li Milin Zhang Wei Han Tao Jiang Yongde Yan 《Journal of Solid State Electrochemistry》2018,22(12):3689-3702
Cyclic voltammogram and square wave voltammograms indicated that Cu (II) ion being reduced to Cu(0) was a two-electron process: Cu(II)?+?e??→?Cu(I) and Cu(I)?+?e??→?Cu(0). The diffusion activation energy for Cu (I) ions was calculated as 42.85 kJ mol?1. The equilibrium potential and apparent standard potential for Cu (I)/Cu(0) redox couple was measured by open circuit chronopotentiometry at a temperature of 773–923 K. Three reduction peaks, corresponding to the formation of PrxCuy intermetallic compounds, were detected from cyclic voltammogram and square wave voltammogram obtained by co-reduction of Pr (III) and Cu (II) or electrodeposition of Pr (III) on Cu electrode. Furthermore, potentiostatic electrolysis was performed to extract the element Pr on Cu electrode, and the electrolytic products were analyzed by scanning electron microscopy equipped with energy dispersive spectrometry. Meanwhile, the highest extraction efficiency of Pr (III) ions could reach about 99.81% at ??2.20 V for 22 h at 823 K. 相似文献
939.
Highly Emissive Fused Heterocyclic Alkynylgold(III) Complexes for Multiple Color Emission Spanning from Green to Red for Solution‐Processable Organic Light‐Emitting Devices 下载免费PDF全文
Dr. Man‐Chung Tang Chin‐Ho Lee Dr. Maggie Ng Yi‐Chun Wong Dr. Mei‐Yee Chan Prof. Dr. Vivian Wing‐Wah Yam 《Angewandte Chemie (International ed. in English)》2018,57(19):5463-5466
A new class of fused heterocyclic tridentate ligand‐containing alkynylgold(III) complexes with tunable emission color has been successfully designed and synthesized. Structural modification of the σ‐donating fused heterocyclic alkynyl ligands, including substituted fluorene, carbazole, and triphenylamine, enables a large spectral shift of about 110 nm (ca. 3310 cm?1) that covers the green to red region to be realized with the same tridentate ligand‐containing alkynylgold(III) complexes in solid‐state thin films. Interestingly, the energy of the excimeric emission can be controlled by the rational design of the fused heterocyclic alkynyl ligands. Superior solution‐processable organic light‐emitting devices (OLEDs) with high external quantum efficiencies (EQEs) of 12.2, 13.5, 9.3, and 5.2 % were obtained with green, yellow, orange, and red emission. These high EQE values are comparable to those of the vacuum‐deposited OLEDs based on structurally related alkynylgold(III) complexes. 相似文献
940.
The title compound, 5-amino-4-cyano-1-[(5-methyl-1-t-butyl-4-pyrazolyl)carbonyl]-3-methylthio-1H-pyrazole 5, was synthesized by the treatment of 4 (5-methyl-1-t-butylpyrazole-4-carbohydrazide) with 2-cyano-3, 3-dimethylthio-acrylonitrile, and its crystal structure was determined by X-ray diffraction method. The crystal belongs to monoclinic, space group P21/c with unit cell parameters a = 13.566(4) Å, b = 10.833(3) Å, c = 11.202(3) Å, α = 90°, β = 98.073(5)°, γ = 90°, V = 1629.9(8) Å3, Z = 4, D
c = 1.298, M
r = 318.40, μ = 0.210 mm−1, F(000) = 672, R
1 = 0.0488 and wR
2 = 0.1250. 相似文献