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991.
Copolyphenylenes with pendant benzimidazolyl and diethanolaminohexyloxy groups: Synthesis and electron‐transporting application in PLEDs
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Chih‐Yang Tseng Wen‐Fen Su Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2017,55(15):2494-2505
Two new electron‐transporting copolyphenylenes P1NH and P2NH possessing balanced charges crucial to emission efficiency of polymer light‐emitting diodes (PLEDs) have been synthesized and applied as an electron‐transporting layer (ETL). The main chain structure is all para‐linkage for P1NH and both para‐ and meta‐linkage for P2NH , with the same pendant electron‐withdrawing benzimidazolyl and polar diethanolaminohexyloxy groups. Both copolymers possess excellent thermal stability (T d > 300 °C, T g > 100 °C) due to their rigid backbones. In addition, the pendant groups effectively lower LUMO (~ ?2.70 eV) and HOMO (~ ?5.70 eV) levels, resulting in improved electron‐transporting and hole‐blocking capabilities. Multilayer yellow‐emitting PLEDs with a configuration of ITO/PEDOT:PSS/SY/ETL/LiF/Al were successfully fabricated by the spin‐coating process. The maximum luminance and maximum current efficiency of the P1NH ‐based device were 12,881 cd/m2 and 10.94 cd/A, respectively, superior to the performance of P2NH ‐based device (4938 cd/m2, 3.70 cd/A) and the device without ETL (8690 cd/m2, 2.78 cd/A). Current results indicate that P1NH is highly effective in enhancing electron transport and device performance. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2494–2505 相似文献
992.
Enzyme Immobilization: Structural Insight into Stabilization of Pickering Emulsions with Fe3O4@SiO2 Nanoparticles for Enzyme Catalysis in Organic Media (Part. Part. Syst. Charact. 7/2017)
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Dr. Chun‐Yi Sun Prof. Xin‐Long Wang Chao Qin Jun‐Ling Jin Zhong‐Min Su Peng Huang Kui‐Zhan Shao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(11):3639-3645
Two anionic metal–organic frameworks (MOFs) with 1D mesoporous tubes ( 1 ) and chiral mesoporous cages ( 2 ) have been rationally constructed by means of a predesigned size‐extended hexatopic ligand, namely, 5,5′,5′′‐(1,3,5‐triazine‐2,4,6‐triyl)tris‐ (azanediyl)triisophthalate (TATAT). Charge neutrality is achieved by protonated dimethylamine cations. Notably, the two MOFs can be used to separate large molecules based on ionic selectivity rather than the size‐exclusion effect so far reported in the literature. Owing to the imino triazine backbone and carboxyl groups of the hexatopic ligand, which provide important host–guest interactions, rare solvatochromic phenomena of 1 and 2 are observed on incorporating acetone and ethanol guests. Furthermore, guest‐dependent luminescence properties of compound 2 were investigated, and the results show that luminescence intensity is significantly enhanced in toluene and benzene, while quenching effects are observed in acetone and ethanol. Thus, compound 2 may be a potential material for luminescent probes. 相似文献
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Ray Kai-Leung Su 《Acta Mechanica Solida Sinica》2011,24(5):429-438
A magnetoelectrically permeable interface crack between two semi-infinite magnetoelectroelastic planes under the action of a heat flow and remote magnetoelectromechanical loadings is considered, where the assumption of frictionless contact between two dissimilar halfplanes is adopted. Not only the solutions of the interface crack problem are presented in an explicit form, but also the general condition for the transition from a perfect thermal contact of two magnetoelectroelastic bodies to their separation is given. 相似文献
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