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61.
The aim of this paper is to show that if the sublinear Emden-Fowler differential equation
(A)  相似文献   
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The Sonogashira coupling of γ‐CD‐encapsulated alkynylpyrenes with terphenyl‐type stopper molecules gave a doubly alkynylpyrene‐threaded [4]rotaxane. The rotaxane showed only excimer emission, with a high fluorescence quantum yield of Φf=0.37, arising from the spatially restricted excimer within the cavity of the γ‐CD. The excimer emission suffered little from self‐quenching up to a concentration of 1.5×10?5 M and was circularly polarized with a high glum value of ?1.5×10?2. The strong circularly polarized luminescence may result from the two stacked pyrenes existing in the rotaxane in an asymmetrically twisted manner.  相似文献   
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Conjugated polyanilines bearing long alkyl side chains (dodecyl PANi-12 and octadecyl PANi-18) were prepared for the purpose of obtaining well-mixed conducting polymer blends with insulating flexible polymers. The miscibility of the polyanilines and ethylene-co-vinyl acetate copolymers (EV A20 with 20 wt % of vinyl acetate and EV A70 with 70 wt %) was significantly improved by long alkyl chains of the same hydrocarbon moieties as the ethylene segments in the matrix EV A, as demonstrated by microscopic observation. PANi-18/EV A20 blends exhibit a lower critical phase separation temperature (LCST). In addition, the EV A crystallinity and the side-chain crystallinity in the miscible blends were depressed, as shown by thermal analysis and x-ray scattering. The comparison of three designed blend systems indicates that the miscibility of the polymers is determined by the hydrophobic interaction between the hydrocarbon units in the both components and by the hydrogen bonding. The solvatochromic phenomena for the blends at low miscible PANi compositions was detected by UV-visible spectroscopy. The threshold conductivities exhibit sensitivity to the morphological structure of the polymeric blends, and was lowered by improved homogenous dispersion of the conducting phase. © 1995 John Wiley & Sons, Inc.  相似文献   
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A series of hole and electron transporting random and block copolymers consisting of triphenylamine moiety as a hole transporting unit and oxadiazole moiety as an electron transporting unit have been prepared via a nitroxide mediated radical polymerization. Oxadiazole monomers with t‐butyl or trifluoromethyl groups, 2 and 7, respectively, were used for copolymerization. Photoluminescent measurements of polymers revealed that the formation of the exciplex between triphenylamine and oxadiazole units tends to occur in the order of random copolymers, block copolymers, and polymer blends, implying phase‐separated morphologies in block or blend systems. The polymers were applied for OLED devices, and we found that the morphology in the polymer layer critically affected device performance. The block copolymer comprising hole and electron transporting units with the composition of 14/86 showed the highest external quantum efficiency over 10%. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1461–1468, 2010  相似文献   
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