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71.
TiO2 decorated with partially crystallized Pd nanoparticles (Pd/TiO2-P) was successfully prepared by atmospheric-pressure dielectric barrier discharge cold plasma. The XRD and XPS analyses proved that Pd ions were reduced to partially crystallized metallic Pd nanoparticles in Pd/TiO2-P. The XPS spectra also indicated that an enhanced metal-support interaction was formed due to the existence of partially crystallized Pd nanoparticles with lower coordination number in Pd/TiO2-P. Photocatalytic activity of Pd/TiO2-P was much higher than that of TiO2 samples decorated with well crystallized Pd nanoparticles. 相似文献
72.
Probing the Rotational Dynamics of meso‐(2‐Substituted)aryl Substituents in A2B‐Type Subporphyrins 下载免费PDF全文
Kota Yoshida Graeme Copley Hirotaka Mori Prof. Dr. Atsuhiro Osuka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(32):10065-10072
A2B‐type B‐methoxy subporphyrins 3 a – g and B‐phenyl subporphyrins 7 a – c , e , g bearing meso‐(2‐substituted)aryl substituents are synthesized, and their rotational dynamics are examined through variable‐temperature (VT) 1H NMR spectroscopy. In these subporphyrins, the rotation of meso‐aryl substituents is hindered by a rationally installed 2‐substituent. The rotational barriers determined are considerably smaller than those reported previously for porphyrins. Comparison of the rotation activation parameters reveals a variable contribution of ΔH≠ and ΔS≠ in ΔG≠. 2‐Methyl and 2‐ethyl groups of the meso‐aryl substituents in subporphyrins 3 e , 3 f , and 7 e induce larger rotational barriers than 2‐alkoxyl substituents. The rotational barriers of 3 g and 7 g are reduced by the presence of the 4‐dibenzylamino group owing to its ability to stabilize the coplanar rotation transition state electronically. The smaller rotational barriers found for B‐phenyl subporphyrins than for B‐methoxy subporphyrins indicate a negligible contribution of SN1‐type heterolysis in the rotation of meso‐aryl substituents. 相似文献
73.
The rates of the hydride abstractions from the 2‐aryl‐1,3‐dimethyl‐benzimidazolines 1a – f by the benzhydrylium tetrafluoroborates 3a – e were determined photometrically by the stopped‐flow method in acetonitrile at 20 °C. The reactions follow second‐order kinetics, and the corresponding rate constants k2 obey the linear free energy relationship log k2(20 °C)= s(N+E), from which the nucleophile‐specific parameters N and s of the 2‐arylbenzimidazolines 1a – c have been derived. With nucleophilicity parameters N around 10, they are among the most reactive neutral C? H hydride donors which have so far been parameterized. The poor correlation between the rates of the hydride transfer reactions and the corresponding hydricities (ΔH0) indicates variable intrinsic barriers. 相似文献
74.
The mechanical properties, morphologies, and gas barriers of hybrid films of cellulose with two different organoclays are
compared. Dodecyltriphenyl-phosphonium-mica (C12PPh-mica) and hexadecyl-mica (C16-mica) were used as reinforcing fillers in the fabrication of the cellulose hybrid films. The cellulose hybrid films were
synthesized from N-methyl-morpholine-N-oxide (NMMO) solutions with the two organo-micas, and solvent-cast at room temperature under vacuum, yielding 15–20 μm thick
films of cellulose hybrids with various clay contents. We found that the addition of only a small amount of organoclay is
sufficient to improve the mechanical properties and gas barriers of the cellulose hybrid films. Even polymers with low organoclay
contents (1–7 wt %) were found to exhibit much higher strength and modulus values than pure cellulose. The addition of C12PPh-mica was more effective than that of C16-mica with regards to the initial tensile modulus, whereas the addition of C16-mica was more effective than that of C12PPh-mica with regards to the gas barrier of the cellulose matrix. The intercalations of the polymer chains in the clays were
examined with wide-angle X-ray diffraction (XRD) and electron microscopy (SEM and TEM). 相似文献
75.
运用B3LYP方法研究了有机钽化合物中分子内α-氢转移反应, 探讨了不同取代基对α-氢转移反应势垒的影响. 确定了反应物、过渡态和产物的几何构型和反应势垒. 结果表明, 过渡金属钽有机化合物中, 发生α-氢转移的碳原子在过渡态中采用sp2杂化. 取代基对α-氢转移势垒的影响取决于取代基对过渡态中碳原子的未参与杂化的pz轨道上单电子的离域作用. Ta(CH3)4CH(SiMe3)2的α-氢转移反应势垒最低. 相似文献
76.
5-氟胞嘧啶气相及水助质子转移异构化的理论研究 总被引:3,自引:0,他引:3
采用密度泛函B3LYP/6-311G**方法,对6种5-氟胞嘧啶异构体孤立分子的稳定性及质子转移引起的酮式-烯醇式、氨基式-亚胺式互变异构反应机理进行了计算研究,获得了零点能、吉布斯自由能及质子转移过程的反应焓、活化能、活化吉布斯自由能和速率常数等参数.计算结果表明,气相中烯醇-氨基式FC4是最稳定的异构体.分子内质子转移设计了FC1→FC2和FC1→FC6两条通道,分别标记为P(1)和P(2),各通道速控步骤的活化能和速率常数分别为155.9 kJ·mol-1,4.70×10-15 s-1和173.1 kJ·mol-1,1.41×10-18 s-1.水助催化时,相应通道P(3) 和P(4) 速控步骤的活化能和速率常数分别为51.0 kJ·mol-1,1.41×103 s-1和88.2 kJ·mol-1,4.53×10-3 s-1.可见,水分子的加入极大地降低了质子转移的活化能垒.另外发现,水分子参与形成协同的双质子转移机理比水助单质子转移机理更利于降低活化能垒. 相似文献
77.
78.
79.
The process of ozone production in pure oxygen using the tubular, high voltage pulse supplied ozonizer was studied. The unusual methodology of conducting kinetics measurements of the ozone synthesis process was presented. It was shown how the process rate changes along the discharge gap. The effect of power density and gas residence time in the discharge gap on the process rate was analysed. The temperature influence on the course of the process, particularly on the ozone boundary concentration and ozone decomposition rate constant, was discussed. 相似文献
80.
Abil E. Aliev Alex J. Sinclair Shen Zhou John D. Wilden Stephen Caddick Dimitri M. Kullmann Dmitri A. Rusakov 《Journal of Physical Organic Chemistry》2009,22(6):607-612
While developing a synthesis towards tagged dizocilpine (MK‐801) analogues, we observed highly restricted inversion of a nitrogen centre in a number hydroxylamines obtained as key intermediates. These compounds are shown to possess some of the structural elements which are expected to significantly hinder the nitrogen inversion, potentially leading to hydroxylamines with a chiral nitrogen centre. Free energy barriers (ΔG≠) of the nitrogen inversion were estimated to be ca. 22 kcal mol?1 at temperatures near 420 K using variable temperature NMR measurements in DMSO‐d6. Further density functional studies of a number model systems were undertaken in order to better rationalize the measured inversion barriers and follow the role of various structural factors in raising the barrier height of the nitrogen inversion process. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献