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The step-wise assembly of the high nuclearity cluster, {[Ni(II)(H2O)5]6[Co(III)(tmphen)2]3[Fe(II)(CN)6]2}13+, is achieved by treating {[Co(tmphen)2]3[Fe(CN)6]2} with six equivalents of Ni(ClO4)2 in aqueous MeOH. 相似文献
114.
Schelter EJ Shatruk M Heintz RA Galán-Mascarós JR Dunbar KR 《Chemical communications (Cambridge, England)》2005,(11):1417-1419
The homoleptic, triphenylborane adduct of the hexacyanochromate anion was structurally characterized and found to be a product in which all six cyanide ligands have undergone isomerization to nitrile groups. 相似文献
115.
WANG Yue BI Xiao-Jun CUI Shu-Wang DING Lin-Kai DAN Zeng-Luo-Bu DING Xiao-Hong FAN Chao FENG Cun-Feng FENG Zhao-Yang FENG Zhen-Yong GAO Xiao-Yu GENG Qing-Xi GUO Hong-Wei HE Hui-Hai HE Mao HU Hai-Bing HU Hong-Bo HUANG Qing JIA Huan-Yu LA Ba-Ci-Ren LE Gui-Ming LI Ai-Feng LI Jin-Yu LOU Yu-Qing LU Hong LU Sui-Ling MENG Xian-Ru MU Jun REN Jing-Ru TAN You-Heng WANG Bo WANG Hui WANG Yong-Gang WU Han-Rong XUE Liang YANG Xian-Chu YE Zong-Hai YU Guang-Ce YUAN Ai-Fang ZHANG Hui-Min ZHANG Ji-Long ZHANG Nai-Jian ZHANG Xue-Yao ZHANG Yong ZHANG Yi ZHA Xi-Sang-Zhu ZHOU Xun-Xiu YUAN Qiang 《中国物理C(英文版)》2008,32(11)
Using the data taken from Tibet Ⅱ High Density (HD) Array (1997 February--1999 September) and Tibet-Ⅲ array (1999 November--2005 November), our previous northern sky survey for TeV γ-ray point sources has now been updated by a factor of 2.8 improved statistics. From 0.0° to 60.0° in declination (Dec) range, no new TeV γ-ray point sources with sufficiently high significance were identified while the well-known Crab Nebula and Mrk421 remain to be the brightest TeV T-ray sources within the field of view of the Tibet air shower array. Based on the currently available data and at the 90% confidence level (C.L.), the flux upper limits for different power law index assumption are re-derived, which are approximately improved by 1.7 times as compared with our previous reported limits. 相似文献
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Spectrophotometric studies of the reactions of iron(II), copper(I) and cobalt(II) with 33 new compounds have demonstrated that the chromogenic properties of diazyl groups are inferior to those of triazyl or pyridyl groups when incorporated into the ferroin chromophore group. The metal complexes of the diazyl derivatives are less stable than those of the corresponding pyridyl and triazyl derivatives. Conditional formation constants of the iron(II) chelates of some representative diazyl derivatives indicate that pyridazyl groups impart greater stabilities than pyrimidyl or pyrazyl groups. Five of the new chromogens have structures that suggest they can chelate iron(II) without steric hindrance, either as bidentate or as terdenate ligands. Although the terdentate mode would ordinarily be expected, two of the five were found to act preferably as bidentate ligands. 相似文献
119.
Wolfgang Scherer Andrew C. Dunbar Jos E. Barquera‐Lozada Dominik Schmitz Georg Eickerling Daniel Kratzert Dietmar Stalke Arianna Lanza Piero Macchi Nicola P. M. Casati Jihaan Ebad‐Allah Christine Kuntscher 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(8):2535-2539
Square‐planar d8‐ML4 complexes might display subtle but noticeable local Lewis acidic sites in axial direction in the valence shell of the metal atom. These sites of local charge depletion provide the electronic prerequisites to establish weakly attractive 3c–2e M⋅⋅⋅H C agostic interactions, in contrast to earlier assumptions. Furthermore, we show that the use of the sign of the 1H NMR shifts as major criterion to classify M⋅⋅⋅H C interactions as attractive (agostic) or repulsive (anagostic) can be dubious. We therefore suggest a new characterization method to probe the response of these M⋅⋅⋅H C interactions under pressure by combined high pressure IR and diffraction studies. 相似文献
120.
Lutterman DA Chouai A Liu Y Sun Y Stewart CD Dunbar KR Turro C 《Journal of the American Chemical Society》2008,130(4):1163-1170
The DNA light-switch complex [Ru(bpy)2(tpphz)]2+ (1, bpy = 2,2'-bipyridine, tpphz = tetrapyrido[3,2-a:2',3'-c:3',2'-h:2',3'-j]phenazine) is luminescent when bound to DNA and in organic solvents and weakly emissive in water. To date, light-switch behavior by transition metal complexes has generally been regarded as confirmation of DNA intercalation. In contrast, the present work demonstrates that the nonintercalating bimetallic complex [(bpy)2Ru(tpphz)Ru(bpy)2]4+ (2) behaves as a DNA light-switch. Weak emission from the 3MLCT excited state of 2 is observed in water with lambda(em) = 623 nm (phi(em) = 1.4 x 10(-4)), and a red shift (lambda(em) = 702 nm) and 40-fold increase in intensity are observed upon addition of 100 microM calf thymus DNA (ct-DNA). Addition of increasing concentrations of 2 to 1 mM herring sperm DNA does not result in an increase in the viscosity of the solution, indicating that the complex is not an intercalator. Additionally, experiments were conducted to ensure that the emission enhancement did not arise from threading intercalation of the complex. The in situ generation of 2 intercalated between the base pairs of ct-DNA in a threading fashion, however, exhibits emission maximum at 685 nm, which is blue-shifted from that of surface-bound 2. DFT calculations show low-lying orbitals in 2 that are expected to exhibit nonemissive character when contributing to the MLCT state, in accord with the lower emission intensity observed for 2 relative to that for 1. To our knowledge, the present work is the first example of a nonintercalating light-switch metal complex, thus showing that light-switch behavior cannot be used exclusively as confirmation of intercalation. 相似文献