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921.
Yuan Chen Lulu Fu Baobao Sun Cheng Qian Dr. Srikala Pangannaya Hong Zhu Prof. Jing Ma Prof. Juli Jiang Dr. Zhigang Ni Prof. Ruibing Wang Prof. Xiancai Lu Prof. Leyong Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(19):5890-5896
Chiral α-amino acids play critical roles in the metabolic process in nearly all life forms. So far, chiral recognition of α-amino acids has mainly focused on the determination of l /d enantiomers. Herein, selection of planar chiral conformations between water-soluble pillar[5]arene WP5 and pillar[6]arene WP6 was observed due to α-side chain or ethyl ester moieties of l -α-amino acid ethyl ester hydrochlorides binding with WP5 and WP6 , respectively. Therefore, α-side chain and ethyl ester moieties of l -α-amino acid ethyl ester hydrochlorides were recognized by observing the induced CD signal and its inversion. This is a rare example of being able to detect the chiral region around α-carbon of a chiral α-amino acid molecule. 相似文献
922.
Extracellular biosynthesis of monodispersed gold nanoparticles by a SAM capping route 总被引:1,自引:0,他引:1
Li Wen Zhonghua Lin Pingying Gu Jianzhang Zhou Bingxing Yao Guoliang Chen Jinkun Fu 《Journal of nanoparticle research》2009,11(2):279-288
Monodispersed gold nanoparticles capped with a self-assembled monolayer of dodecanethiol were biosynthesized extracellularly
by an efficient, simple, and environmental friendly procedure, which involved the use of Bacillus megatherium D01 as the reducing agent and the use of dodecanethiol as the capping ligand at 26 °C. The kinetics of gold nanoparticle
formation was followed by transmission electron microscope (TEM) and UV-vis spectroscopy. It was shown that reaction time
was an important parameter in controlling the morphology of gold nanoparticles. The effect of thiol on the shape, size, and
dispersity of gold nanoparticles was also studied. The results showed that the presence of thiol during the biosynthesis could
induce the formation of small size gold nanoparticles (<2.5 nm), hold the shape of spherical nanoparticles, and promote the
monodispersity of nanoparticles. Through the modulation of reaction time and the use of thiol, monodispersed spherical gold
nanoparticles capped with thiol of 1.9 ± 0.8 nm size were formed by using Bacillus megatherium D01. 相似文献
923.
924.
Tianyu Sun Jianyong Ma Xiaoyong Fu Jianpeng Wang Yunxia Jin Jianda Shao Zhengxiu Fan 《中国光学快报(英文版)》2010,(5):447-448
<正>A guided-mode resonance(GMR) filter with the same material(Ta_2O_5) for both the grating layer and the waveguide layer is designed and fabricated.This simple structure is easy to fabricate and can avoid the defects at the grating/waveguide interface using different materials.The spectral response measured with a Lambda 900 spectrophotometer under normal incidence for TE waves exhibits a peak reflectance exceeding 80%at the wavelength of 1040 nm with a full-width half-maximum(FWHM) linewidth of 23 nm.We evaluate the deviations of the fabricated structure from the designed parameters. 相似文献
925.
Xiubo Jiang Yi Shi Wen Zhu Yongming Chen Fu Xi 《Journal of polymer science. Part A, Polymer chemistry》2012,50(20):4239-4245
Well‐defined mikto‐topology star polystyrene composed of one cyclic arm and four linear arms was synthesized by a combination of atom transfer radical polymerization (ATRP) and Cu‐catalyzed azide‐alkyne cycloaddition (CuAAC) click reaction. First, the bromine‐alkyne α,ω‐linear polystyrenes containing four hydroxyl groups protected with acetone‐based ketal groups were synthesized by ATRP of styrene using a designed initiator. Then, the bromine end‐group was converted to the azide and the linear polystyrene was cyclized intra‐molecularly by the CuAAC reaction. The four hydroxyl groups were released by deprotection and then esterified with 2‐bromoisobutyryl bromide to produce a cyclic polymer bearing four ATRP initiating units. By subsequent ATRP of styrene to grow linear polymers with the cyclic polystyrene as a macroinitiator, the mikto‐topology star polymers were prepared. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
926.
Experimental study has been performed on nanosecond (ns) laser ablation of silicon at 1064 nm, through which a so-called “multi-pulse enhancement effect” has been revealed, which has been rarely reported in literature. The major features of this effect are: (1) for multi-pulse laser ablation at the same spatial location, the ablation efficiency increases as the pulse number increases and the pulse-to-pulse temporal distance decreases; (2) for multi-pulse ablation performed sequentially at a group of locations, the ablation quality and efficiency starting from the second location can be significantly enhanced if the distance between adjacent locations is sufficiently small. Further study is needed to confirm and understand the underlying physical mechanism for the multi-pulse enhancement effect, which can be utilized to significantly improve the quality and efficiency of laser silicon micromachining using the low-cost and low-energy-consumption infrared ns lasers. This may decrease the cost and energy consumption of many relevant areas, such as the solar cell industry. 相似文献
927.
A Pd-catalyzed coupling reaction of ArBr/ArCl/ArOTf with sodium thiosulfate takes place in presence of Cs2CO3 at 80 °C. The reaction mixture is directly treated with Zn/HCl to afford aryl thiols in good to excellent yields. 相似文献
928.
Ye Wu Irene Ling Li Ling Fu Jian pang Zhai Shuang Chen Ruan 《Applied Surface Science》2009,255(23):9409-9412
Excimer laser emitting at 248 nm is applied to produce microstructures on the surface of aluminum alloy. The surface morphology shows that hotspots and thermal fluidic structures both come to light. Two possible mechanisms of hotspots formation are proposed: near-field diffraction and interference, and extremely fast rapid thermal annealing. And for the formation of thermal fluidic pattern structure, a thin film model is applied. 相似文献
929.
Zirconium-based metal-organic framework materials (Zr−MOFs) have more practical usage over most conventional benchmark porous materials and even many other MOFs due to the excellent structural stability, rich coordination forms, and various active sites. However, their mass-production and application are restricted by the high-cost raw materials, complex synthesis procedures, harsh reaction conditions, and unexpected environmental impact. Based on the principles of “Green Chemistry”, considerable efforts have been done for breaking through the limitations, and significant progress has been made in the sustainable synthesis of Zr−MOFs over the past decade. In this review, the advancements of green raw materials and green synthesis methods in the synthesis of Zr−MOFs are reviewed, along with the corresponding drawbacks. The challenges and prospects are discussed and outlooked, expecting to provide guidance for the acceleration of the industrialization and commercialization of Zr−MOFs. 相似文献
930.
Michael Addition Catalyzed by Chiral Secondary Amine Phosphoramide Using Fluorinated Silyl Enol Ethers: Formation of Quaternary Carbon Stereocenters
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Jin‐Sheng Yu Fu‐Min Liao Wei‐Ming Gao Kui Liao Run‐Lin Zuo Prof. Dr. Jian Zhou 《Angewandte Chemie (International ed. in English)》2015,54(25):7381-7385
A chiral secondary amine phosphoramide was developed and identified as a powerful catalyst for the Mukaiyama–Michael addition of fluorinated enol silyl ethers to tetrasubstituted olefins. The resulting products are obtained with high enantioselectivities and contain a quaternary carbon stereocenter bearing either a difluoroalkyl or monofluoroalkyl group. 相似文献