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41.
为将生物体内微观的蛋白行为可视化并以宏观信号呈现出来对蛋白进行实时、动态分析,借助SNAP-tag蛋白标签技术与有机小分子荧光染料,构建了一系列用于活细胞内实时监测目标蛋白的免洗荧光探针。标签蛋白SNAP-tag能够特异性识别探针中的苄基鸟嘌呤,从而使目标蛋白共价连接上荧光团(萘酰亚胺),携带上荧光信使。此外,由于萘酰亚胺从水环境中被牵引至SNAP-tag蛋白的疏水空腔,其荧光信号呈现出2~13倍的增强。通过SNAP-tag标签蛋白与目标蛋白的融合,该荧光探针实现了对活细胞内线粒体蛋白CoX8A及核内蛋白H2B特异性识别,在免洗条件下完成了对目标蛋白的实时追踪及原位分析。 相似文献
42.
43.
末端碳链长度对偶氮苯自组装膜结构的影响 总被引:4,自引:0,他引:4
The end-group dominated molecular orientation in the azobenzene self-assembled monolayers (SAMs), CnAzoC2SH (n=1-4), on gold was evaluated for the first time by grazing incidence reflection absorption FTIR spectroscopy (RA-FTIR). All these azobenzene SAMs have highly-organized and closely-parked structures, with the molecule tilting away gradually from surface normal direction with the increase of end group alkyl length. 相似文献
44.
45.
With P(CH3)3 as the probe molecule adsorbed on titanium silicalite (TS-1) zeolite, the special and important role of T12 site in MFI-type zeolite was clearly elucidated. There are altogether three active sites present in TS-1 zeolite with Ti at the T12 site. Owing to the preferential adsorption of probe molecules on the first Brönsted acidic site, the Ti12 center will probably fail to show Lewis acidity. The ionic [HP(CH3)3]+ species can be stabilized by the first or second Brönsted acidic site, with the former energetically favored. The latter was formed through the transfer of the ionic [HP(CH3)3]+ species from the first to the second Brönsted acidic site. 相似文献
46.
von Niessen Wolfgang Cederbaum Lorenz S. Kraemer Wolfgang P. 《Theoretical chemistry accounts》1977,44(1):85-93
The vertical valence ionization potentials of cyclopropane, ethylene oxide and ethylene imine are calculated by a many-body Green's function method. For C3H6 the ordering of the ionization potentials is 2e(), 1e(), 2a1(), 1a2(), 1e(). The assignment of the 2a1 and the 1a2 ionization potentials which has been controversial is thus clarified. The ordering is in agreement with the result obtained via Koopmans' theorem. For ethylene oxide and ethylene imine Koopmans' theorem fails in predicting the correct order of ionic states. For C2H4O the ordering of the ionization potentials is 2b
1(), 4a
1, 1a
2(), 2b
2,3a
1, 1b
1(), 1b
2, 2a
1 and for C2H5N 6a, 5a, 3a, 2a, 4a, 3a, 1a, 2a. The agreement of the computed ionization potentials with the experimental values is very satisfactory. 相似文献
47.
报导了α,ω-偶氮苯,紫精双发色团化合物的合成与性质研究,结果表明偶氮苯的光致顺反异构化以可调控与之相连的紫精与曙红络合行为,其作用程度的强弱与连接两者的亚甲基链的长度有关,借助HNMR通过对构象进行分析解释了上述的研究结果。 相似文献
48.
利用自组装技术在金电极表面构造了具有不同前端健长度偶氮苯功能化的单分子膜体系:Au/S(CH2)nNHCO-N=N-OCH2CH3(n=2,3,4,6).研究结果表明,仍氮苯到金电极的表现电子转移速率随它们之间的距离长度的增加而呈指数性的下降趋势.基于Marcus电子隧穿理论,得到了此自组装膜体系的长程电子隧穿系数ρ=(1.35±0.2)/CH2在和可逆电活性分子自组装膜体系及理论计算相比较的基础上,从偶氮苯分子自组装膜结构与电子转移过程的关系角度对这一结果进行了分析和说明. 相似文献
49.
N. S. Mosyagin A. V. Titov R. J. Buenker H.‐P. Liebermann A. B. Alekseyev 《International journal of quantum chemistry》2002,88(5):681-686
Multireference single‐ and double‐excitation configuration interaction (MRD‐CI) calculations of transition energies for the Hg atom and spectroscopic constants for the HgH molecule are carried out with the generalized relativistic effective core potential (GRECP) method. A new selection criterium for the reference configurations is discussed. The calculated spectroscopic constants are compared with experimental data and results of calculations of other groups. Improvement of accuracy is mainly observed for bond lengths from the GRECP/MRD‐CI calculations (without applying the T = 0 correction) with respect to the results of other groups. Analysis of the quality of the approximations employed is carried out. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002 相似文献
50.
Elettra L. Piacentino Edwin Rodriguez Kevin Parker Thomas M. Gilbert Richard A. J. O'Hair Victor Ryzhov 《Journal of mass spectrometry : JMS》2019,54(6):520-526
Gas‐phase C―C coupling reactions mediated by Ni (II) complexes were studied using a linear quadrupole ion trap mass spectrometer. Ternary nickel cationic carboxylate complexes, [(phen)Ni (OOCR1)]+ (where phen = 1,10‐phenanthroline), were formed by electrospray ionization. Upon collision‐induced dissociation (CID), they extrude CO2 forming the organometallic cation [(phen)Ni(R1)]+, which undergoes gas‐phase ion‐molecule reactions (IMR) with acetate esters CH3COOR2 to yield the acetate complex [(phen)Ni (OOCCH3)]+ and a C―C coupling product R1‐R2. These Ni(II)/phenanthroline‐mediated coupling reactions can be performed with a variety of carbon substituents R1 and R2 (sp3, sp2, or aromatic), some of them functionalized. Reaction rates do not seem to be strongly dependent on the nature of the substituents, as sp3‐sp3 or sp2‐sp2 coupling reactions proceed rapidly. Experimental results are supported by density functional theory calculations, which provide insights into the energetics associated with the C―C bond coupling step. 相似文献