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101.
Amr L. Saber 《Electroanalysis》2010,22(24):2997-3002
Simple, selective and accurate sensors were developed for the determination of melatonin and oxomemazine in biological samples (urine) and in pharmaceutical preparations. Potentiometric measurements were based on bismus tetraiodate‐drug ion‐pair as novel electroactive materials incorporating a plasticized PVC membrane with o‐nitrophenyl octyl ether or dioctyl phthalate. Each sensor was conditioned for at least two days in 0.1 M drug solution before use. It exhibited fast and stable Nernstian response for melatonin and oxomemazine over the concentration range of 1.0×10?6–1.0×10?2 M and 1.0×10?5–1.0×10?2 M, pH range of 3.0–6.5 and 3.5–6.0 for melatonin and oxomemazine sensors, respectively. Results with an average recovery not more than 101 % and a mean standard deviation less than 1.0 % of the nominal were obtained for the four sensors. The sensors showed reasonable selectivity towards investigated drugs in presence of many cations. 相似文献
102.
Hugo J. Bohórquez Chérif F. Matta Russell J. Boyd 《International journal of quantum chemistry》2010,110(13):2418-2425
The local single particle momentum is proposed as a localized‐electrons detector (LED) that provides a direct three‐dimensional representation of bonding interactions in molecules. It is given exclusively in terms of the electron density and its gradient. We show that the graphical representation of bonding interactions given by LED is consistent with the local curvatures of the electron density as given by the eigenvalues of the Hessian matrix, according to a local symmetry classification of the critical points here introduced. LED consistently complements the topological analysis of the electron density given by the quantum theory of atoms in molecules, by providing a graphical representation of the symmetry of the bonding interactions in molecular systems. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem 110:2418–2425, 2010 相似文献
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Francesca Tessore Dr. Elena Cariati Prof. Franco Cariati Prof. Dominique Roberto Prof. Renato Ugo Prof. Patrizia Mussini Prof. Cristiano Zuccaccia Dr. Alceo Macchioni Prof. 《Chemphyschem》2010,11(2):495-507
A series of 4‐X‐1‐methylpyridinium cationic nonlinear optical (NLO) chromophores (X=(E)‐CH?CHC6H5; (E)‐CH?CHC6H4‐4′‐C(CH3)3; (E)‐CH?CHC6H4‐4′‐N(CH3)2; (E)‐CH?CHC6H4‐4′‐N(C4H9)2; (E,E)‐(CH?CH)2C6H4‐4′‐N(CH3)2) with various organic (CF3SO3?, p‐CH3C6H4SO3?), inorganic (I?, ClO4?, SCN?, [Hg2I6]2?) and organometallic (cis‐[Ir(CO)2I2]?) counter anions are studied with the aim of investigating the role of ion pairing and of ionic dissociation or aggregation of ion pairs in controlling their second‐order NLO response in anhydrous chloroform solution. The combined use of electronic absorption spectra, conductimetric measurements and pulsed field gradient spin echo (PGSE) NMR experiments show that the second‐order NLO response, investigated by the electric‐field‐induced second harmonic generation (EFISH) technique, of the salts of the cationic NLO chromophores strongly depends upon the nature of the counter anion and concentration. The ion pairs are the major species at concentration around 10?3 M , and their dipole moments were determined. Generally, below 5×10?4 M , ion pairs start to dissociate into ions with parallel increase of the second‐order NLO response, due to the increased concentration of purely cationic NLO chromophores with improved NLO response. At concentration higher than 10?3 M , some multipolar aggregates, probably of H type, are formed, with parallel slight decrease of the second‐order NLO response. Ion pairing is dependent upon the nature of the counter anion and on the electronic structure of the cationic NLO chromophore. It is very strong for the thiocyanate anion in particular and, albeit to a lesser extent, for the sulfonated anions. The latter show increased tendency to self‐aggregate. 相似文献
106.
The infrared and visible cooperative emissions of ytterbium ions are studied in Yb-doped NdVO4 single crystals. The absorption of optical phonons allows the emissions at room temperature when a Nd:YAG laser is used. Low temperature emissions are observed due to the Nd3+→Yb3+ energy transfer following an argon ion laser excitation of the Nd3+ ions. Analysis of the cooperative emission at low doping concentration (1%) indicates that it is generated by distant pair forming Yb3+ ions while at high doping concentration (≥ 5%) close ions magnetically coupled and superexchange mechanisms prevail in the emitting process. 相似文献
107.
Separate spatial soliton pairs in a biased series centrosymmetric photorefractive crystal circuit 总被引:1,自引:0,他引:1
It is shown theoretically that three types of separate soliton pairs: bright-bright, bright-dark, and dark-dark, can be established in a biased series circuit consisting of two centrosymmetric photorefractive crystals and the two solitons in a separate soliton pair can affect each other by the light-induced current. The effects of the intensities of soliton beams and background lights on the normalized profiles of solitons are discussed. 相似文献
108.
姚裕丰 《纯粹数学与应用数学》2014,(1):1-6
通过计算及归纳的方法,得到了n×n矩阵代数中极大线性无关的反交换2-幂零矩阵的个数,推广了相关文献中的一般线性李代数gl(n)的交换子代数的最大维数这一结论. 相似文献
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《代数通讯》2013,41(11):4133-4140
Abstract The aim of this work is to provide characterizations, up to isomorphism, of the standard embedding and the Lister enveloping of an associative pair. We shall obtain it using basic facts on homological algebra. This paper intends to simplify the use of both envelopes. 相似文献