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A series of star-shaped octupolar triazatruxenes (TATs, 1-6) with intramolecular "push-pull" structure were synthesized and their photophysical properties have been systematically investigated. These chromophores showed obvious solvatochromic effect, i.e., significant bathochromic shift of the emission spectra and larger Stokes shifts were observed in more polar solvents mainly due to photoinduced intramolecular charge transfer (ICT). The two-photon absorption (2PA) cross-section values were determined by two-photon excited fluorescence (2PEF) measurements in toluene and THF. These chromophores exhibited large two-photon absorption cross-sections ranging from 280 to 1620 GM in the near-infrared (NIR) region. Compound 6 showed the largest 2PA action cross-section (σ(2)Φ) of 564 GM and could be a potential two-photon fluorescent (2PF) probe. In addition, compounds 1-6 all displayed good thermal stability and photostability. 相似文献
174.
Jiang-Sheng Han Yin-Lin Shao Xiao-Hong Zhang Ping Zhong 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):1599-1610
Abstract An efficient and green aqueous protocol to access 3-chalcogen benzo[b]furan derivatives has been developed. The reaction can proceed via I2-mediated intramolecular annulation reaction of 2-alkynylanisoles with diaryl disulfides (diselenides) in water or under solvent-free conditions at room temperature. With the participation of I2, a variety of 3-chalcogen benzo[b]furan derivatives were obtained in good to excellent yields. This reaction was considered to work via an iodocyclization cascade mechanism and the intermediate 3-iodo-2-phenylbenzofuran was detected by GC-MS. 相似文献
175.
CO2部分氧化乙烷制乙烯Pd—Cu/MoO3—SiO2催化剂的研究 总被引:7,自引:0,他引:7
用化学吸附-红外光谱、化学吸附-程序升温脱附(TPD)和微型反应技术研究了Pd-Cu/MoO3-SiO2(MoSO)催化剂对CO2和乙烷的吸附活化和部分氧化反应性能.结果表明,乙烷以C—H键中的H吸附于MoSO载体表面MoO键的端基氧上;Pd-Cu/MoSO催化剂对CO2有良好的化学吸附活化性能,CO2的吸附除有线式吸附态和剪式吸附态外,还有一种新的卧式吸附态;Pd-Cu/MoSO催化剂的晶格氧参与了化学反应.探讨了在Pd-Cu/MoSO催化剂上CO2的部分氧化乙烷反应机理 相似文献
176.
Synthesis of hydrothermally stable and long-range ordered Ce-MCM-48 and Fe-MCM-48 materials 总被引:1,自引:0,他引:1
The hydrothermally stable and long-range ordered Ce-MCM-48 and Fe-MCM-48 were conveniently synthesized at 393 K for 24 h by directly adding fluoride ions to the initial gel without posttreatment and pH adjustment. The Ce-MCM-48 with a Si/Ce of 200 and 100, which were prepared by directly adding fluoride ions, could still maintain their mesoporous structures after refluxing in boiling water for 3 days. The incorporation of Ce into MCM-48 could enhance the hydrothermal stability of MCM-48 in the absence of fluoride ions; however, the incorporation of Fe into MCM-48 materials barely improved the hydrothermal stability of MCM-48 materials. The effect of adding NaF was much more efficient in enhancement of hydrothermal stability than that of the incorporation of Ce. The addition of fluoride ions mainly improves the degree of polymerization of silicates. The Ce(4+) ions in Ce-MCM-48 appear to be present partly in tetrahedral coordination in the framework and partly as CeO(2) particles on the surface of framework. The Ce positioned on the surface of pore walls and in the framework both provide the protection against water attack. 相似文献
177.
Kadish KM Phan TD Giribabu L Shao J Wang LL Thuriere A Van Caemelbecke E Bear JL 《Inorganic chemistry》2004,43(3):1012-1020
Eleven different Ru(2)(4+) and Ru(2)(3+) derivatives are characterized by thin-layer FTIR and UV-visible spectroelectrochemistry under a CO atmosphere. These compounds, which were in-situ electrogenerated from substituted anilinopyridine complexes with a Ru(2)(5+) core, are represented as Ru(2)(L)(4)Cl where L = 2-CH(3)ap, ap, 2-Fap, 2,3-F(2)ap, 2,4-F(2)ap, 2,5-F(2)ap, 3,4-F(2)ap, 3,5-F(2)ap, 2,4,6-F(3)ap, or F(5)ap. The Ru(2)(5+) complexes do not axially bind CO while mono- and bis-CO axial adducts are formed for the Ru(2)(4+) and Ru(2)(3+) derivatives, respectively. Six of the eleven investigated compounds exist in a (4,0) isomeric form while five adopt a (3,1) geometric conformation. These two series of compounds thus provide a large enough number of derivatives to examine trends and differences in the spectroscopic data of the two types of isomers in their lower Ru(2)(4+) and Ru(2)(3+) oxidation states. UV-visible spectra of the Ru(2)(4+) derivatives and IR spectra of the Ru(2)(3+) complexes under CO are both isomer dependent, thus suggesting that these data can be used to reliably predict the isomeric form, i.e., (3,1) or (4,0), of diruthenium complexes containing four unsymmetrical substituted anilinopyridinate bridging ligands; this was confirmed by X-ray crystallographic data for seven compounds whose structures were available. 相似文献
178.
Chuan Jie Cheng Quan Lei Fu Xiong Xiong Bai Shao Jin Liu Liang Shen Wu Qin Fan Hong Xia Li 《Chemical Papers》2013,67(3):336-341
A novel cationic gemini surfactant has been readily synthesised in 70 % total yield. The functional gemini surfactant can act both as an emulsifier and an atom transfer radical polymerisation (ATRP) initiator in mini-emulsion polymerisation of methyl methacrylate (MMA), in which no other emulsifier was required. 1-(Dimethylamino)dodecane (N,N-dimethyldodecylamine, DMDA) was found to be a good ligand in the activator generated by electron transfer (AGET) ATRP reaction. Kinetic studies indicated that the polymerisation featured controlled/living radical polymerisation. 相似文献
179.
The hydrogen abstraction reaction of O(^3P) with Si2H6 has been studied theoretially. Two transition states of ^3A″ and ^3A′ symmetries have been located for this abstraction reaction. Geometries have been optimized at the UMP2 leve with 6-311G (d) basis set. G3MP2 has been used for the final single-point energy calculation. The rate constants have been calculated over a wide temperature range of 200-3000K using canonical variational transition-state sheory (CVT) with small curvature tunneling effect(SCT). The calculated CVT/SCT rate constants match well with the experimental value. 相似文献
180.