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1.
Deliang Kong Lihua Guo Meng Tian Shumiao Zhang Zhenzhen Tian Huayun Yang Ye Tian Zhe Liu 《应用有机金属化学》2019,33(1)
Fifteen organometallic Ir(III) half‐sandwich complexes ( 1A – 5C ) having the general formula [(η5‐Cpx)Ir(N^N)Cl]PF6 (Cpx = Cp*, tetramethyl(phenyl)cyclopentadienyl (Cpxph) or tetramethyl(biphenyl)cyclopentadienyl (Cpxbiph); N^N = diamine) have been synthesized and characterized. The molecular structure of 1A was determined using single‐crystal X‐ray diffraction analysis. The hydrolysis of 1A – 5C was monitored using UV–visible spectra. Complexes 3A – 3C showed catalytic activity for the oxidation of NADH to NAD+, where 3C showed the highest turnover number of 29.9 within 450 min. Cytotoxicity examination by MTT assay was carried out against two human cancer cell lines (HeLa and A549) after 24 or 48 h drug treatment. The complexes showed high potency, where the most potent complex ( 3C ; IC50 = 3.4 μM) was six times more active than cisplatin against A549 cells after 24 h drug exposure. Cytotoxic potency towards A549 cells increased with phenyl substitution on Cp ring: Cpxbiph > Cpxph > Cp*. In addition, the biological studies showed that 3C caused cell apoptosis and cell cycle arrest at G1 phase in A549 cancer cells. Moreover, 3C increased the level of reactive oxygen species markedly after 24 h, which may provide an important basis for killing cancer cells. Confocal laser scanning microscopy was used to track 3C in A549 cells. The cellular localization experiment showed that 3C targeted lysosomes and caused lysosomal damage. 相似文献
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Rongrong Li Hongjie Peng Qingping Wu Xuejun Zhou Jiang He Hangjia Shen Minghui Yang Chilin Li 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(29):12227-12236
Herein, we propose the construction of a sandwich-structured host filled with continuous 2D catalysis–conduction interfaces. This MoN-C-MoN trilayer architecture causes the strong conformal adsorption of S/Li2Sx and its high-efficiency conversion on the two-sided nitride polar surfaces, which are supplied with high-flux electron transfer from the buried carbon interlayer. The 3D self-assembly of these 2D sandwich structures further reinforces the interconnection of conductive and catalytic networks. The maximized exposure of adsorptive/catalytic planes endows the MoN-C@S electrode with excellent cycling stability and high rate performance even under high S loading and low host surface area. The high conductivity of this trilayer texture does not compromise the capacity retention after the S content is increased. Such a job-synergistic mode between catalytic and conductive functions guarantees the homogeneous deposition of S/Li2Sx, and avoids thick and devitalized accumulation (electrode passivation) even after high-rate and long-term cycling. 相似文献
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In this paper, the bending fatigue tests of honeycomb sandwich panels are carried out by using an improved three-point bending test fixture, and the S-N curves at different stress ratios are obtained. Through the records of fatigue damage in the experiment, the failure mode of the honeycomb sandwich panels and the source of fatigue damage are determined. At the same time, through the calculation of the shear stress distribution on the honeycomb wall, the reasons for the difference in the failure morphology of the L-direction and W-direction sandwich panels are clarified. Besides, a life prediction method is proposed and its effectiveness in predicting the fatigue life of sandwich panels has been verified. 相似文献
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New cage models (MeAlO)n(Me3Al)m (n=16, m=6 or 7) isomeric with previously reported sheet models for the principle activator found in hydrolytic MAO (h-MAO) are compared at M06-2X and MN15 levels of theory using density functional theory with respect to their thermodynamic stability. Reactivity of the neutrals or corresponding anions with formula [(MeAlO)16(Me3Al)6Me]− towards chlorination, and loss of Me3Al is explored while reactivity of the neutrals towards formation of contact- and outer-sphere ion pairs from Cp2ZrMe2 and Cp2ZrMeCl is examined. The results suggest on balance that a cage model for this activator is less consistent with experiment than an isomeric sheet model, although the latter are more stable based on free energy. 相似文献
8.
Prof. Dr. Holger Braunschweig Charlotte Brückner Dr. Mehmet Ali Celik Dr. Klaus Dück Dr. Florian Hupp Dr. Thomas Kramer Johannes Krebs Dr. Ivo Krummenacher 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(31):11056-11064
Taking advantage of an improved synthesis of [Ti(η6‐C6H6)2], we report here the first examples of ansa‐bridged bis(benzene) titanium complexes. Deprotonation of [Ti(η6‐C6H6)2] with nBuLi in the presence of N,N,N′,N′′,N′′‐pentamethyldiethylenetriamine (pmdta) leads to the corresponding 1,1′‐dilithio salt [Ti(η6‐C6H5Li)2] ? pmdta that enables the preparation of the first one‐ and two‐atom‐bridged complexes by simple salt metathesis. The ansa complexes were fully characterized (NMR spectroscopy, UV/Vis spectroscopy, elemental analysis, and X‐ray crystallography) and further studied electrochemically and computationally. Moreover, [Ti(η6‐C6H6)2] is found to react with the Lewis base 1,3‐dimethylimidazole‐2‐ylidene (IMe) to give the bent sandwich complex [Ti(η6‐C6H6)2(IMe)]. 相似文献
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Ansa‐Complexes of [Mn(η5‐C5H5)(η6‐C6H6)]: Preparation,Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3) 下载免费PDF全文
Prof. Dr. Holger Braunschweig Dr. Alexander Damme Dr. Klaus Dück Dr. Marco Fuß Dr. Christian Hörl Dr. Thomas Kramer Dr. Ivo Krummenacher Dr. Thomas Kupfer Valerie Paprocki Christoph Schneider 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(42):14797-14803
We report the synthesis of [n]manganoarenophanes (n=1, 2) featuring boron, silicon, germanium, and tin as ansa‐bridging elements. Their preparation was achieved by salt‐elimination reactions of the dilithiated precursor [Mn(η5‐C5H4Li)(η6‐C6H5Li)]?pmdta (pmdta=N,N,N′,N′,N′′‐pentamethyldiethylenetriamine) with corresponding element dichlorides. Besides characterization by multinuclear NMR spectroscopy and elemental analysis, the identity of two single‐atom‐bridged derivatives, [Mn(η5‐C5H4)(η6‐C6H5)SntBu2] and [Mn(η5‐C5H4)(η6‐C6H5)SiPh2], could also be determined by X‐ray structural analysis. We investigated for the first time the reactivity of these ansa‐cyclopentadienyl–benzene manganese compounds. The reaction of the distannyl‐bridged complex [Mn(η5‐C5H4)(η6‐C6H5)Sn2tBu4] with elemental sulfur was shown to proceed through the expected oxidative addition of the Sn?Sn bond to give a triatomic ansa‐bridge. The investigation of the ring‐opening polymerization (ROP) capability of [Mn(η5‐C5H4)(η6‐C6H5)SntBu2] with [Pt(PEt3)3] showed that an unexpected, unselective insertion into the Cipso?Sn bonds of [Mn(η5‐C5H4)(η6‐C6H5)SntBu2] had occurred. 相似文献
10.
片状材料的径厚比是片状材料的一个重要特征参数。以片状云母为研究对象,引入形状明显区别于片状云母的聚苯乙烯球作为支撑材料。实验结果表明,当云母片与聚苯乙烯球混合质量比为1∶3时,呈竖立取向云母片的数量达到最大值,随机采集200个云母片的长径和厚度,其径厚比的统计样本均值为15.37。支撑材料聚苯乙烯球为片状云母带来大量支撑位点,显著提高片状云母呈竖立取向的概率,能够快速、直观地同时测量云母片的长径和厚度,有效提高云母片径厚比的测量效率和准确性。 相似文献