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Michal Kohout Alexej Bubnov Jiří Šturala Vladimíra Novotná Jiří Svoboda 《Liquid crystals》2016,43(10):1472-1485
Two series of new liquid crystalline lactic acid derivatives with a terminal ester group have been synthesised. The effect of this ester unit and the length of its alkyl chain on the mesomorphic and dielectric properties of the compounds exhibiting a broad temperature range of chiral smectic phases have been studied. We found that the mesomorphic behaviour and phase transition temperatures are strongly affected by the molecular architecture. Depending on the alkyl chain length in the terminal ester unit, the studied materials exhibited paraelectric smectic A*, ferroelectric tilted smectic C* and antiferroelectric smectic CA* phases over a broad temperature range. The physical properties of the compounds have been studied by optical polarising microscopy, differential scanning calorimetry, electro-optic measurements, small-angle X-ray scattering and dielectric spectroscopy. Furthermore, the homologues with short terminal alkyl chains showed a very small layer shrinkage at the transition from the orthogonal SmA* to the tilted SmC* phase, which is a characteristic feature of ‘de Vries-type’ behaviour. 相似文献
63.
Dan Archdeacon Charles J. Colbourn Isidoro Gitler J. Scott Provan 《Journal of Graph Theory》2000,33(2):83-93
A graph is YΔY‐reducible if it can be reduced to a vertex by a sequence of series‐parallel reductions and YΔY‐transformations. Terminals are distinguished vertices, that cannot be deleted by reductions and transformations. In this article, we show that four‐terminal planar graphs are YΔY‐reducible when at least three of the vertices lie on the same face. Using this result, we characterize YΔY‐reducible projective‐planar graphs. We also consider terminals in projective‐planar graphs, and establish that graphs of crossing‐number one are YΔY‐reducible. © 2000 John Wiley & Sons, Inc. J Graph Theory 33: 83–93, 2000 相似文献
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Reactions of one or two equiv. of cyclohexyl isocyanide in THF at room temperature with Mo?Mo triply bonded complexes [Mo(CO)2(η5‐C5H4R)]2 (R=COCH3, CO2CH3) gave the isocyanide coordinated Mo? Mo singly bonded complexes with functionally substituted cyclopentadienyl ligands, [Mo(CO)2(η5‐C5H4R)]2(μ‐η2‐CNC6H11) ( 1a , R=COCH3; 1b , R=CO2CH3) and [Mo(CO)2(η5‐C5H4R)(CNC6H11)]2 ( 2a , R=COCH3; 2b , R=CO2CH3), respectively. Complexes 1a , 1b and 2a , 2b could be more conveniently prepared by thermal decarbonylation of Mo? Mo singly bonded complexes [Mo(CO)3(η5‐C5H4R)]2 (R=COCH3, CO2CH3) in toluene at reflux, followed by treatment of the resulting Mo?Mo triply bonded complexes [Mo(CO)2(η5‐C5H4R)]2 (R=COCH3, CO2CH3) in situ with cyclohexyl isocyanide. While 1a , 1b and 2a , 2b were characterized by elemental analysis and spectroscopy, 1b was further characterized by X‐ray crystallography. 相似文献
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Liang Song Chunlai Tu Yunfeng Shi Feng Qiu Lin He Yi Jiang Qi Zhu Bangshang Zhu Deyue Yan Xinyuan Zhu 《Macromolecular rapid communications》2010,31(5):443-448
A simple approach to tune the optical properties of the hyperbranched conjugated polymers by only adjusting the terminal‐backbone interactions has been reported in this article. Hyperbranched conjugated polyazomethines have been successfully prepared by the reaction of tetramine and dialdehyde. Not only varying the monomer feed ratio to change the quantity of terminal amino groups, but also adopting protonation or complexion with proper dopants (SnCl2 and β‐cyclodextrin), can alter the interactions between amino terminals and imine bonds in the backbone. Correspondingly, the optical properties of the resulting hyperbranched polymers are controlled.
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空间激光通信凭借其带宽优势,成为未来高速空间通信不可或缺的有效手段,是近年来国际上的研究热点。本文详细介绍了美国、欧洲和日本在空间激光通信技术领域的最新研究进展和未来发展规划,总结了国内外空间激光通信演示计划的主要参数指标。通过对空间激光通信最新研究计划的分析,归纳出空间激光通信高速化、深空化、集成化、网络化、一体化5个发展趋势,以及需要突破的高阶调制、高灵敏度探测、多制式兼容、"一对多"通信等关键技术。为我国激光通信设备及相关研究提供借鉴和参考。 相似文献
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A facile and practical synthetic route of unsymmetrical 1,3‐diynes via the PdCl/CuI catalyzed oxidative coupling of two different terminal alkynes has been developed by using 3‐(diphenylphosphino)propanoic acid as a ligand in the presence of oxygen. This system is suitable for not only aromatic alkynes but also heteroaromatic and aliphatic alkynes which were transformed into the corresponding unsymmetrical 1,3‐diynes in moderate to good yields at room temperature. Moreover, the unsymmetrical 1,3‐diynes were also obtained on a multi‐gram scale. Mechanistic studies suggest that oxygen plays a key role in the catalytic cycles. 相似文献