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Selective oxidation of sulfides to sulfoxides was successfully performed by employing readily available Fe(NO3)3·9H2O as the active catalyst with oxygen as the oxidant in 2,2,2-trifluoroethanol (TFE) without the formation of sulfones. Nitrate anion could play a crucial role in promoting the reaction due to the oxidation capacity under acidic media. High yields of sulfoxides were exclusively obtained from the corresponding sulfides. Furthermore, both aromatic and aliphatic sulfides gave moderate to high yields of sulfoxides with this protocol. 相似文献
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Xiang Ying Shi Jue Lin Ziyang Li Tao Jin-Wang Huang Liang-Nian Ji 《Liquid crystals》2013,40(2):211-214
We observed that the planar aligned nematic liquid crystal (5CB) doped with a volume fraction of 1% of FeTPPCl [5,10,15,20-tetraphenylporphyriniron(III)chloride] or MnTPPCl [5,10,15,20-tetraphenylporphyrinmanganese(III)chloride] dramatically decreased the critical magnetic field for the magnetic field induced Freedericksz transition, while 5CB doped with ZnTPP [5,10,15,20-tetraphenylporphyrinzinc(II)] revealed no such effect, when compared with pure 5CB. In the guest-host (5CB) system, FeTPPCl and MnTPPCl as guests are both strong paramagnetic materials with an interaction through coordination of the -CN group in 5CB onto the metal ion of the porphyrin. As a result, the 5CB molecules are dragged to reorientate under a static magnetic field, while ZnTPP is a diamagnetic material without such a property. This phenomenon concerning magneto-optical components could be useful in liquid crystal displays. 相似文献
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双-锌卟啉对DABCO分子识别的立体构象及其热力学研究 总被引:2,自引:1,他引:1
合成了系列不同长度以柔性侧链相连的p/p型双-锌卟啉配合物,用1H NMR和UV-Vis研究了不同温度下该系列配合物与刚性双齿配体DABCO(1,4-二氮杂双环)的轴向配位反应,考察了侧链长度对双-锌卟啉与配体的分子识别能力影响。结果表明,主体分子双-锌卟啉可以对客体分子BABCO进行分子识别,合适长度的柔韧烷氧链可以调节主体分子的构象,使DABCO嵌入双卟啉两个卟啉环间空位中,形成锌卟啉-DABCO-锌卟啉三元夹心式配合物构象。探讨了配位反应中立体构象的变化过程,并测定了热力学参数。 相似文献
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Jin-Hua Cai Jin-Wang Huang Ping Zhao Yuan-Jian Ye Han-Cheng Yu Liang-Nian Ji 《Journal of Sol-Gel Science and Technology》2009,50(3):430-436
Three types of novel silica-metalloporphyrins hybrid materials, Si-S-APTCPPFe, Si-S-APTCPPMn and Si-S-APTCPPCo, were prepared
at room temperature by sol–gel method involving a thiol-ene polymerization reaction of 5-(4-allyloxy)phenyl-10,15,20-tri(4-chlorophenyl)porphyrin
(APTCPP) with 3-mercaptopropyltrimethoxysilane (MPS). The hybrid materials were characterized by XRD, SEM, FT–IR, UV–Vis and
TG, and were investigated as catalysts for the aerobic oxidation of cyclohexane. It is found that these hybrid materials are
more efficient catalysts than the analogous non-supported metalloporphyrins for cyclohexane hydroxylation in metalloporphyrin–O2–ascrobate system and the metal ion in the porphyrins significantly affected the catalytic efficiencies of these hybrid materials. 相似文献
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Bin Peng Xiang Chen Ke-Jie Du Bo-Le Yu Hui Chao Liang-Nian Ji 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,74(4):896-901
A novel ligand dipyrido[1,2,5]oxadiazolo[3,4-b]quinoxaline (dpoq) and its complexes [Ru(bpy)2(dpoq)]2+ and [Ru(phen)2(dpoq)]2+ (bpy = 2,2′-bipyridine; phen = 1,10-phenanthroline) have been synthesized and characterized by elemental analysis, electrospray mass spectra and 1H NMR. The interaction of Ru(II) complexes with calf thymus DNA (CT-DNA) was investigated by absorption spectroscopy, fluorescence spectroscopy, thermal denaturation and viscosity measurements. Results suggest that two Ru(II) complexes bind to DNA via an intercalative mode. 相似文献