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21.
Yong Zhao Xianliang Sheng Jin Zhai Lei Jiang Chunhe Yang Zhongwei Sun Yongfang Li Daoben Zhu 《Chemphyschem》2007,8(6):856-861
Titanium dioxide (TiO(2)) photoelectrodes with micro/nano hierarchical branched inner channels have been prepared by an electrohydrodynamic (EHD) technique and assembled to form dye-sensitized solar cells (DSSCs). Excellent penetration of ionic-liquid electrolytes and enhanced light harvesting in the longer wavelength region are realized within the composite-structure electrode, thus a better fill factor (ff) of 75.3 % and higher conversion efficiency (eta) of 7.1 % are obtained for viscous ionic-liquid electrolytes compared to pure nanostructured films. Hierarchical branched channels in the photoanodes can efficiently improve the transport properties of redox-active species in viscous electrolytes, which is demonstrated by electrical impedance spectroscopy (EIS). The incident monochromatic photon-to-electron conversion efficiency (IPCE) shows that enhanced light scattering in the composite film is of benefit for light harvesting and thus for solar energy conversion efficiency. 相似文献
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Conjugate additions of amino alcohols derived from alpha-amino acids to vinyl sulfones, followed by N-benzylation, chlorination, and intramolecular alkylation, provide a convenient route to substituted pyrrolidines. The process is accompanied by the stereospecific rearrangement of substituents from the alpha-position of the amine to the beta-position of the product and takes place via the corresponding aziridinium ion intermediates. Another type of rearrangement was observed during the reaction of (2-piperidine)methanol or 2-(2-piperidine)ethanol with phenyl trans-1-propenyl sulfone, in which the methyl group appears to migrate from the beta- to the alpha-position of the sulfone moiety. This process involves the isomerization of phenyl trans-1-propenyl sulfone to phenyl 2-propenyl sulfone by the addition-elimination of catalytic benzenesulfinate anion to the former vinyl sulfone, followed by conjugate addition of the amino group to the latter sulfone. Chlorination and intramolecular alkylation then afford the corresponding rearranged indolizidine and quinolizidine derivatives, respectively. 相似文献
24.
Pt(PPh_3)_2Cl_2在碱性介质中,与一氧化碳直接进行还原及羰基化反应,得到五种膦取代的羰基铂配合物:Pt_5(μ_2-CO)_5(CO)(PPh_3)_4 1,Pt_3(μ_2-CO)_3(PPh_3)_3 2,Pt_3(μ_2-CO)_3(PPh_3)_4 3,Pt_4(μ_2-CO)_5(PPh_3)_4 4,以及Pt(Cl)(PPh_3)_2(COOCH_3) 5。经X-射线单晶衍射分析,确定了新的三核铂羰基簇2以及配合物5的分子结构。还讨论了1和5的生成机理。 相似文献
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Mesoporous molecular sieves were synthesized from Beta and Fau zeolite precursors through S+X−I+ route under extremely acidic conditions in parallel (designated as MBeta and MFau, respectively). The textural properties of MFau were different from its MBeta counterpart but resembled normal MCM-41 silica from TEOS. Al content in MBeta was almost equivalent to that in the initial Beta zeolite precursors, whereas only trace Al species was present in MFau from elemental analysis results. The hydrothermal stability of MBeta after post-synthesis ammonia treatment was considerably improved compared with normal MCM-41 aluminosilicates, whereas the MFau after the same procedure was as unstable as normal MCM-41 silica. Thus, the assembly behaviors of Beta and Fau zeolite precursors were comparatively studied based on these results. The microstructure of Fau zeolite precursors were degraded by the extremely acidic condition, and Al species was dissolved into the synthesis mixture. However, Beta zeolite precursors survived the chemical attack of extremely acidic media and were incorporated into mesostructured framework as primary building units. 相似文献
27.
Yunhui Zhai Xijun Chang Yuemei Cui Ning Lian Shoujun Lai Hong Zhen Qun He 《Mikrochimica acta》2006,154(3-4):253-259
A rapid, selective method that utilize 4-(2-Pyridylazo)-resorcinol (PAR)-modified nanometer SiO2 (nanometer SiO2–PAR) as a new solid-phase extractant for preconcentration of trace mercury (II) has been developed. The adsorption property
of nanometer SiO2–PAR for metal ions was studied by selectively extracting different metal ions from aqueous solutions. The results revealed
an excellent affinity of the nanometer SiO2–PAR for mercury (II) in presence of interfering metal ions at pH 4. The main parameters of solid-phase extraction such as
shaking time, elution and sample dilution effect were studied. The extractant shows rapid kinetic sorption, and the adsorption
equilibrium of mercury (II) on nanometer SiO2–PAR was achieved in less than 2 min. The adsorbed mercury (II) was easily eluted by 4 mL of 6 mol L−1 HCl. The maximum preconcentration factor was 50. The maximum static adsorption capacity was 276 μmol g−1 at pH 4. The detection limit (3σ) was 0.43 μg L−1 for cold vapor atomic absorption spectrometry (CVAAS), and the relative standard deviation of the eight replicate determinations
was 2.4% for the determination of 2.0 μg of Hg(II) in 100 mL water sample. The method was applied to the determination of
trace mercury (II) in sample solutions with satisfactory results. 相似文献
28.
In this paper, the voltammetric method was used for the first time to study the effect of Cisplatin-liposome on Hela cells. The results showed the voltammetric behavior of Hela cells was irreversible and the peak current had linear relationship with the cell number. With both Cisplatin-liposome concentration and treating time increasing, the peak current decreased. The peak current decreasing was in accordance with the nuclear damage and loss of mitochondrial membrane potential revealed by two-photon laser scanning microscopy and confocal laser scanning microscopy. This voltammetric method may provide a simple way to study the electron-transfer mechanism in drug-treating cells. 相似文献
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Becattini B Sareth S Zhai D Crowell KJ Leone M Reed JC Pellecchia M 《Chemistry & biology》2004,11(8):1107-1117
Bid is a key member of the Bcl-2 family proteins involved in the control of the apoptotic cascade in cells, leading to cell death. Uncontrolled cell death is associated with several human pathologies, such as neurodegenerative diseases and ischemic injuries. Therefore, Bid represents a potential yet unexplored and challenging target for strategies aimed at the development of therapeutic agents. Here we show that a multidisciplinary NMR-based approach that we named SAR by ILOEs (structure activity relationships by interligand nuclear Overhauser effect) allowed us to rationally design a series of 4-phenylsulfanyl-phenylamine derivatives that are capable of occupying a deep hydrophobic crevice on the surface of Bid. These compounds represent the first antiapoptotic small molecules targeting a Bcl-2 protein as shown by their ability to inhibit tBid-induced SMAC release, caspase-3 activation, and cell death. 相似文献