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71.
In the present study, the concept of the output frequency response function is applied to theoretically investigate the force transmissibility of multi-degree of freedom (MDOF) structures with a nonlinear anti-symmetric viscous damping. The results reveal that an anti-symmetric nonlinear viscous damping can significantly reduce the transmissibility over all resonance regions for MDOF structures while it has almost no effect on the transmissibility over non-resonant and isolation regions. The results indicate that the vibration isolators with an anti-symmetric damping characteristic have great potential to overcome the dilemma in the design of linear viscously damped vibration isolators where an increase of the damping level reduces the force transmissibility over resonant region but increases the transmissibility over non-resonant regions. 相似文献
72.
Björn Geißler Oliver Kolb Jens Lang Günter Leugering Alexander Martin Antonio Morsi 《Mathematical Methods of Operations Research》2011,73(3):339-362
We introduce a mixed integer linear modeling approach for the optimization of dynamic transport networks based on the piecewise
linearization of nonlinear constraints and we show how to apply this method by two examples, transient gas and water supply
network optimization. We state the mixed integer linear programs for both cases and provide numerical evidence for their suitability. 相似文献
73.
Dou Ma Ping Li Xiangyu Duan Jiazhen Li Pengpeng Shao Zhongling Lang Lixia Bao Yuanyuan Zhang Zhengguo Lin Bo Wang 《Angewandte Chemie (International ed. in English)》2020,59(10):3905-3909
Metal–organic frameworks (MOFs) with long‐term stability and reversible high water uptake properties can be ideal candidates for water harvesting and indoor humidity control. Now, a mesoporous and highly stable MOF, BIT‐66 is presented that has indoor humidity control capability and a photocatalytic bacteriostatic effect. BIT‐66 (V3(O)3(H2O)(BTB)2), possesses prominent moisture tunability in the range of 45–60 % RH and a water uptake and working capacity of 71 and 55 wt %, respectively, showing good recyclability and excellent performance in water adsorption–desorption cycles. Importantly, this MOF demonstrates a unique photocatalytic bacteriostatic behavior under visible light, which can effectively ameliorate the bacteria and/or mold breeding problem in water adsorbing materials. 相似文献
74.
Tianbo Li Fang Chen Rui Lang Hua Wang Yang Su Botao Qiao Aiqin Wang Tao Zhang 《Angewandte Chemie (International ed. in English)》2020,59(19):7430-7434
The hydroformylation of olefins is one of the most important homogeneously catalyzed industrial reactions for aldehyde synthesis. Various ligands can be used to obtain the desired linear aldehydes in the hydroformylation of aliphatic olefins. However, in the hydroformylation of aromatic substrates, branched aldehydes are formed preferentially with common ligands. In this study, a novel approach to selectively obtain linear aldehydes in the hydroformylation of styrene and its derivatives was developed by coupling with a water–gas shift reaction on a Rh single‐atom catalyst without the use of ligands. Detailed studies revealed that the hydrogen generated in situ from the water–gas shift is critical for the highly regioselective formation of linear products. The coupling of a traditional homogeneous catalytic process with a heterogeneous catalytic reaction to tune product selectivity may provide a new avenue for the heterogenization of homogenous catalytic processes. 相似文献
75.
Ji‐Long Shi Rufan Chen Huimin Hao Cheng Wang Xianjun Lang 《Angewandte Chemie (International ed. in English)》2020,59(23):9088-9093
2D covalent organic frameworks (COFs) are receiving ongoing attention in semiconductor photocatalysis. Herein, we present a photocatalytic selective chemical transformation by combining sp2 carbon‐conjugated porphyrin‐based covalent organic framework (Por‐sp2c‐COF) photocatalysis with TEMPO catalysis illuminated by 623 nm red light‐emitting diodes (LEDs). Highly selective conversion of amines into imines was swiftly afforded in minutes. Specifically, the π‐conjugation of porphyrin linker leads to extensive absorption of red light; the sp2 ?C=C? double bonds linkage ensures the stability of Por‐sp2c‐COF under high concentrations of amine. Most importantly, we found that crystalline framework of Por‐sp2c‐COF is pivotal for cooperative photocatalysis with (2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl (TEMPO). This work foreshadows that the outstanding hallmarks of COFs, particularly crystallinity, could be exploited to address energy and environmental challenges by cooperative photocatalysis. 相似文献
76.
Jihui Lang Xue Li Jinghai Yang Lili Yang Yongjun Zhang Yongsheng YanQiang Han Maobin Wei Ming Gao Xiaoyan Liu Rui Wang 《Applied Surface Science》2011,257(22):9574-9577
ZnO quantum-dot chains codoped with Eu3+ and Er3+ were synthesized by the chemical precipitation method and the codoping effects on the structures, morphologies and optical properties of the powders were briefly investigated. The X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) results indicated the Eu3+ and Er3+ were incorporated into the crystal lattice of ZnO host. Transmission electron microscope (TEM) measurements showed the sizes of the ZnO quantum dots decreased with the increase of Eu3+ and Er3+ doping concentration, and the quantum-dot chains were formed by codoping with Eu3+ and Er3+. The green emissions in the photoluminescence spectra were attributed to 4f-4f of Er3+ inner shell 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 transitions, and the characteristic red emissions of Eu3+ ions were attributed to the 5D0 → 7F1 and 5D0 → 7F2 transitions, respectively. Moreover, the red emission of the Eu3+ ions gradually decreased with the Er3+ ions doping concentration increased, which may be due to the different energy storage centers in the powders. 相似文献
77.
78.
Min-Jie Shi Sheng-Zhong Kou Bao-Shou Shen Jun-Wei Lang Zhi Yang Xing-Bin Yan 《中国化学快报》2014,25(6):859-864
Ionic liquid gel polymers have widely been used as the electrolytes in all-solid-state supercapacitors, but they suffer from low ionic conductivity and poor electrochemical performance. Arc discharge is a fast, low-cost and scalable method to prepare multi-layered graphene nanosheets, and as-made graphene nanosheets (denoted as ad-GNSs) with few defects, high electrical conductivity and high thermal stability should be favorable conductive additive materials. Here, a novel ionic liquid gel polymer electrolyte based on an ionic liquid (EM1MNTF2) and an copolymer (P(VDF-HFP)) was modified by the addition of ad-GNSs as an ionic conducting promoter. This modified gel electrolyte shows excellent thermal stability up to 400 ℃ and a wide electrochemical window of 3 V. An all-solid-state supercapacitor based on commercial activated carbon was fabricated using this modified ionic liquid gel polymer electrolyte, which shows obviously improved electrochemical behaviors compared with those of the corresponding all-solid-state supercapacitor using pure ionic liquid gel polymer electrolyte. Specially, smaller internal resistance, higher specific capacitance, better rate performance and cycling stability are achieved. These results indicate that the ionic liquid gel polymers modified by ad-GNSs would be promising and suitable gel electrolytes for high performance all-solid-state electrochemical devices. 相似文献
79.
Photoionization and Pyrolysis of a 1,4‐Azaborinine: Retro‐Hydroboration in the Cation and Identification of Novel Organoboron Ring Systems 下载免费PDF全文
Fabian Holzmeier Dipl.‐Chem. Melanie Lang Dr. Patrick Hemberger Dr. Andras Bodi Dipl.‐Chem. Marius Schäfer Dr. Rian D. Dewhurst Prof. Dr. Holger Braunschweig Prof. Dr. Ingo Fischer 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(31):9683-9692
The photoionization and dissociative photoionization of 1,4‐di‐tert‐butyl‐1,4‐azaborinine by means of synchrotron radiation and threshold photoelectron photoion coincidence spectroscopy is reported. The ionization energy of the compound was determined to be 7.89 eV. Several low‐lying electronically excited states in the cation were identified. The various pathways for dissociative photoionization were modeled by statistical theory, and appearance energies AE0K were obtained. The loss of isobutene in a retro‐hydroboration reaction is the dominant pathway, which proceeds with a reverse barrier. Pyrolysis of the parent compound in a chemical reactor leads to the generation of several yet unobserved boron compounds. The ionization energies of the C4H6BN isomers 1,2‐ and 1,4‐dihydro‐1,4‐azaborinine and the C3H6BN isomer 1,2‐dihydro‐1,3‐azaborole were determined from threshold photoelectron spectra. 相似文献
80.
An efficient method of ligand-free Cu-catalyzed oxidative decarboxylative homocoupling of aryl propiolic acids was developed. When CuI was employed as the catalyst and I2 as the oxidant, the decarboxylative homocoupling reaction for Csp–Csp bond formation in DMSO underwent smoothly to afford the corresponding 1,4-disubstituted 1,3-dialkynes in good to excellent yields without any organic ligands. This catalytic system was applicable to aryl propiolic acids bearing different steric, electronic, and functional groups. 相似文献