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A new bulky 2-chloro-5,10,15-tris(2,4,6-triphenylphenyl)-corrole was casually synthesized and the effect of mono-β-chlorination on its photophysical, electrochemical properties and light-induced singlet oxygen generation was investigated.  相似文献   
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‘Axial-bonding’-type hetero trimers have been constructed by employing a simple ‘inorganic’ reaction such as axial bond formation of main group element containing phosphorus corrole. The approach is simple and modular in nature. The architecture of these hetero trimers such that, while a phosphorus(V)corrole forms the basal scaffolding unit, either two free-base porphyrins [(H 2 ) 2 –PCor] or ZnII porphyrins [(Zn) 2 –PCor] occupy the two axial sites via an aryloxy bridge. Both hetero trimeric species have been completely characterized by mass (FAB), UV/Vis, proton nuclear magnetic resonance spectroscopies and also by the differential pulse voltammetric method. Comparison of their spectroscopic and electrochemical data of these trimers with those of the corresponding reference compounds reveal that there is no apparent ring-to-ring interactions in these ‘vertically’ linked hetero trimers. Reduced fluorescence quantum yields were observed for [(H 2 ) 2 –PCor] and [(Zn) 2 –PCor] when compared to corresponding monomeric chromophores. Finally, a comparison is made between the presently reported phosphorus(V)corrole based hetero arrays and the previously reported analogous arrays based on Ge(IV)corrole with regard to their spectroscopic properties and photochemical activities.  相似文献   
3.
A simple, straightforward, and scalable procedure for the preparation of 2-bromofuran using N-bromosuccinimide (NBS) in dimethylformamide (DMF) is reported. The described preparation is conducted on a 20 to 50 g scale and does not require extractive workup procedures or chromatographic purifications. To illustrate the synthetic applications of 2-bromofuran, palladium-catalyzed Suzuki coupling reactions of the prepared 2-bromofuran with various aryl boronic acids were investigated, and moderate to good yields of 2-arylfurans were obtained.  相似文献   
4.
Details on the structure and transport characteristics of the solid polymer electrolyte polyethylene oxide (PEO)/lithium salt (LiClO4) modified by novolac phenolic resin are presented here. From IR spectra it could be concluded that complex formation occurred through multiple interactions between the ether oxygen of PEO–lithium, phenolic lithium, and the phenolic ether oxygen of PEO. The free hydroxyl band in phenolic reflected that phenolic closely interacted with both the PEO polymer and ionic salt. With increasing salt content in PEO, the vibration band corresponding to the ClO anion (~623 cm?1) displayed growth of a shoulder at ~635 cm?1, suggesting the formation of Li+…ClO4? ion pairing. However, in the presence of phenolic, ion‐pairing formation was effectively suppressed, which suggested that the phenolic moiety facilitated a greater degree of LiClO4 salt dissociation. Activation energy analysis revealed two conducting pathways: one through the amorphous PEO and the other through the PEO/phenolic amorphous matrix. The high ion conductivity originated from effective salt dissociation and the establishment of a new conduction network formed by PEO and phenolic. Furthermore, the structural modification also extended the thermal stability and mechanical strength of the solid polymer electrolyte composite. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3866–3875, 2004  相似文献   
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