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Polymer electrolyte membrane based on polyacrylate with phosphonic acidvia long alkyl side chains
Higashihara, Tomoya,Fukuzaki, Namiko,Tamura, Youko,Rho, Yecheol,Nakabayashi, Kazuhiro,Nakazawa, Satoshi,Murata, Shigeaki,Ree, Moonhor,Ueda, Mitsuru The Royal Society of Chemistry 2013 Journal of Materials Chemistry A Vol.1 No.4
Higashihara Tomoya,Inoue Kyoichi,Nagura Masato,Hirao Akira The Polymer Society of Korea 2006 Macromolecular Research Vol.14 No.3
To successively synthesize star-branched polymers, we developed a new iterative methodology which involves only two sets of the reactions in each iterative process: (a) an addition reaction of DPE or DPE-functionalized polymer to a living anionic polymer, and (b) an in-situ reaction of 1-(4-(4-bromobutyl)phenyl)-1-phenylethylene with the generated 1,1-diphenylalkyl anion to introduce one DPE functionality. With this methodology, 3-, 4-, and 5-arm, regular star-branched polystyrenes, as well as 3-arm ABC, 4-arm ABCD, and a new 5-arm ABCDE, asymmetric star-branched polymers, were successively synthesized. The A, B, C, D, and E arm segments were poly(4-trimethylsilylstyrene), poly(4-methoxystyrene), poly(4-methylstyrene), polystyrene, and poly(4-tert-butyldimethylsilyloxystyrene), respectively. All of the resulting star-branched polymers were well-defined in architecture and precisely controlled in chain length, as confirmed by SEC, $^1H$ NMR, VPO, and SLS analyses. Furthermore, we extended the iterative methodology by the use of a new functionalized DPE derivative, 1-(3-chloromethylphenyl)-1-((3-(1-phonyletheny1)phenyl) ethylene, capable of introducing two DPE functionalities via one DPE anion reaction site in the reaction (b). The number of arm segments of the star-branched polymer synthesized by the methodology could be dramatically increased to 2, 6, and up to 14 by repeating the iterative process.
Tomoya Higashihara,Mitsuru Ueda 한국고분자학회 2013 Macromolecular Research Vol.21 No.3
Polymer-based solar cells (PSCs) have been promising candidates as renewable energy resources, having multiple advantages of flexible, low-cost and large-area processing for their mass production. Among them, much attention has been paid to fundamental bulk-heterojunction (BHJ) devices using a blend of regioregular poly(3-hexylthiophene)(P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as the active layer. However, there are still significant limitations not only in the low power conversion efficiency (PCE), but also in the device stability. The morphological control of BHJ PSCs is one of the most important issues to improve the device performances. On the other hand, P3HT itself has received much attention in many fields, because it is the best class of balanced high-performance materials as a p-type semiconductor in terms of solubility, chemical stability, charge mobility, and commercial availability. The discovery of the quasi-living Grignard metathesis polymerization (or called catalysttransfer polycondensation) system has made it possible to synthesize a wide variety of chain-end-functional P3HT derivatives, their block copolymers and star-branched polymers. Since the competitive research areas including PSC applications have strongly demanded the accelerated developments of new materials and well-defined morphologies related to polythiophenes, the fundamental studies of P3HT have still been targeted by many research groups. In this review, the controlled synthesis of P3HT, the synthesis of P3HT-based block copolymers, their applications to PSCs,as well as the scope and potential of new thiophene-based materials are described.