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61.
Peng Li  Zhuo Chai  Shi-Zheng Zhu 《Tetrahedron》2009,65(8):1673-1678
Pd-catalyzed direct arylation of 3-fluorofurans with a variety of aryl bromides was facilitated by the neighboring effect of fluorine atom to provide tetrasubstituted monofluoro furans in moderate to good yields.  相似文献   
62.
Several fluorine containing polycyclic aromatic hydrocarbons with exact carbon atom topology of the C60 fullerene have been synthesized. Different numbers of fluorine atoms were introduced in the key positions, as needed for an efficient intramolecular condensation to the fullerene molecule. The polycyclic aromatic compounds obtained represent attractive precursors for rational, high-yield fullerene synthesis by flash vacuum pyrolysis.  相似文献   
63.
Iodine was used to catalyze the hetero-Diels-Alder reaction of pentafluorobenzylidineaniline (C6F5CHNAr 1) with enol ethers to afford the corresponding tetrahydroquinolines derivatives as a mixture of cis/trans stereoisomers in moderate yields. These products could also be prepared by one-pot, three-component reaction of pentafluorophenylaldehyde, anilines, and enol ethers under the same reaction condition. Mild and neutral reaction conditions, facile experimental procedure, and low price of iodine should make this method attractive for practical synthesis of many fluorinated tetrahydroquinoline derivatives.  相似文献   
64.
The synthesis of new polyfluorinated dendrimeric metallophthalocyanines (M = Zn, Ni, Co) bearing 3,5-bis(2′,3′,4′,5′,6′-pentafluorobenzyloxy)benzyloxy moieties (24) was achieved by cyclotetramerization of phthalonitrile derivative 1 in the presence of zinc, nickel or cobalt salts in DMF. All the target phthalocyanines were separated by column chromatography and their spectroscopic, fluorescence and energy transfer properties, and aggregation behavior were investigated in different solvents and at different concentrations in chloroform. The compounds were characterized by Fourier transform-infrared, fluorine, proton and carbon nuclear magnetic resonance, mass, ultraviolet–visible and fluorescence spectral data. The phthalocyanines (24) were extremely soluble in various organic solvents, such as tetrahydrofuran, acetone and dichloromethane.  相似文献   
65.
Synthetic approach based on mediated addition of different trifluoromethylated building blocks to selected acyclic imines giving access to a variety of β-hydroxy-β-trifluoromethyl imines are elaborated. A reaction between fluorinated adducts and imines proceed easily giving the condensation products in good to excellent yields. β-Hydroxy-β-trifluoromethyl imines possessing trifluoromethyl group and exhibiting strong intramolecular hydrogen bonding are great precursors to different β-hydroxy-β-trifluoromethyl ketones and alcohols.  相似文献   
66.
The synthesis of several 2-(substituted fluorobenzoylimino)-3-(substituted fluorophenyl)-4-methyl-1,3-thiazolines (2a-t) was carried out by base-catalyzed cyclization of corresponding 1-(fluorobenzoyl)-3-(fluorophenyl)thioureas (1a-t) with 2-bromoacetone in aqueous medium. The structures of the synthesized compounds were confirmed by spectral and elemental analysis. All synthesized compounds were evaluated for in vitro antibacterial activity using Gram-positive bacteria (Staphylococcus aureus, Bacillus subtilis) and Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa). The minimum inhibitory concentration (MIC) was determined for the most active compounds. In vitro antifungal activity was also determined against the five fungal species (Rhizopus oryzae, Fusarium oxysporum, Aspergillus terreus, A. niger and A. fumigatus).  相似文献   
67.
CF3CFBr2 was employed in catalytic olefination reactions of aromatic aldehydes. In situ prepared hydrazones of aldehydes were transformed to β-fluoro-β-(trifluoromethyl)styrenes by reaction with CF3CFBr2 under CuCl catalysis. Based on this reaction, a novel stereoselective approach towards β-fluoro-β-(trifluoromethyl)styrenes was elaborated. Nucleophilic vinylic substitution of fluorine by secondary amines, thiolates and alkoxides in β-fluoro-β-(trifluoromethyl)styrenes was also tested.  相似文献   
68.
以异佛尔酮二异氰酸酯(IPDI)、十二氟庚醇(FOH)、烯丙基聚乙二醇(APEG)合成的表面活性含氟单体(FSM)与丙烯酰胺通过水溶液聚合,制备出含氟疏水缔合聚丙烯酰胺(FPAM).用表面张力法研究了FSM的胶束化,用流变仪、动态激光光散射(DLS)和原子力显微镜(AFM)表征了FPAM溶液的流变性能、缔合结构尺寸和形态.结果表明,FSM在25℃下CMC为1.28 g.L-1,表面张力为26.77 mN.m-1.FPAM溶液属于假塑性体系,临界缔合浓度为0.660%,具有一定的耐盐性.DLS和AFM表明,在低于临界缔合浓度时FPAM溶液仍能产生大量的缔合结构,FPAM分子具有很强的疏水缔合性.  相似文献   
69.
A series of high luminescent europium complexes have been synthesized, such as Eu(TFNB)3phen (1), Eu(PFNP)3phen (2), Eu(HFNH)3phen (3) and Eu(PFND)3phen (4), which have β-diketone ligands containing fluorinated alkyl chains with different lengths and conjugated naphthyl groups, i.e., 4,4,4-trifluoro-1-(2-naphthyl)butane-1,3-dione (TFNB); 4,4,5,5,5-pentafluoro-1-(2-naphthyl)pentane-1,3-dione (PFNP); 4,4,5,5,6,6,6-heptafluoro-1-(2-naphthyl)hexane-1,3-dione (HFNH) and 4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-pentadecafluoro-1-(2-naphthyl)decane-1,3-dione (PFND). And 10-phenanthroline (phen) is coordinated as the neutral second ligand in 1-4. The crystal structures of 1 and 2 have been studied, which are typical and similar to that of 3. The results of TGA-DTA suggest that these Eu complexes have good thermal stabilities. By means of absorption and (time resolved) emission spectroscopy including determination of luminescence quantum yields, energy transfer dynamics and so on, the following results have been obtained: first, these Eu complexes show characteristic pure red color photoluminescence emission with high quantum efficiencies from the central Eu3+ ions through the excitation of the ligands; secondly, photophysical properties of 1, 2, 3 and 4, especially the lifetimes of excited states 5D0 of Eu3+ ions and quantum efficiencies are influenced by the different lengths of fluorinated alkyl chains, though the singlets (S1) and triplets (T1) of the fluorinated ligands are almost the same.  相似文献   
70.
Low surface energy polymer thin-films can be applied to surfaces to increase hydrophobicity and reduce friction for a variety of applications. However, wear of these thin films, resulting from repetitive rubbing against another surface, is of great concern. In this study, we show that highly hydrophobic surfaces with persistent abrasion resistance can be fabricated by depositing fluorinated carbon thin films on sandblasted glass surfaces. In our study, fluorinated carbon thin films were deposited on sandblasted and as-received smooth glass using deep reactive ion etching equipment by only activating the passivation step. The surfaces of the samples were then rubbed with FibrMet abrasive papers in a reciprocating motion using an automatic friction abrasion analyzer. During the rubbing, the static and kinetic friction forces were also measured. The surface wetting properties were then characterized using a video-based contact angle measuring system to determine the changes in water contact angle as a result of rubbing. Assessment of the wear properties of the thin films was based on the changes in the water contact angles of the coated surfaces after repetitive rubbing. It was found that, for sandblasted glass coated with fluorinated carbon film, the water contact angle remained constant throughout the entire rubbing process, contrary to the smooth glass coated with fluorinated carbon film which showed a drastic decrease in water contact angle with the increasing number of rubbing cycles. In addition, the static and kinetic friction coefficients of the sandblasted glass were also much lower than those of the smooth glass.  相似文献   
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