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Soluble and processable conjugated polyazines with oligo(p-phenylene vinylene)s

机译:可溶和可加工的具有低聚(对亚苯基亚乙烯基)的共轭聚嗪

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摘要

An efficient polycondensation reaction between alpha,omega-diformyl functional aromatics,namely 2,5-diheptyloxy-1,4-diforrnylbenzene and side-chain substituted alpha,omega-diformyl oligo(p-phenylene vinylene) (OPV) with hydrazine afforded novel soluble and processable conjugated polymers,P1 and P2,respectively.The reaction conditions were investigated and structural analysis of the polymers was carried out by means of 1H,13C,15N NMR,indicating all-trans configured C=N-N=C linkages.The molecular weights M_n were observed at ~1100-1400 g/mol for P1 and approx 8700-10,500 g/mol for P2.The optical properties showed absorption maxima at ~455 nm and ~487 nm for P1 and P2 (CHC13 solutions),respectively,red shifted by 31-60 nm relative to the monomer aromatics due to conjugation through the azine linkage.The emission maxima are observed at ~515 nm and ~560 nm for P1 and P2 (CHC13 solutions),respectively.Thin films of P2 readily undergo n-doping.
机译:α,ω-二甲酰基官能芳族化合物,即2,5-二庚氧基-1,4-二甲酸苯与侧链取代的α,ω-二甲酰基低聚对苯乙炔(OPV)与肼之间的有效缩聚反应提供了新的可溶性研究了反应条件,并通过1H,13C,15N NMR进行了聚合物的结构分析,表明全反式构型的C = NN = C键。 P1的M_n约为〜1100-1400 g / mol,P2的M_n约为8700-10,500 g / mol。光学性能显示P1和P2(CHC13溶液)分别在〜455 nm和〜487 nm处有最大吸收。由于通过嗪键的共轭作用,相对于单体芳族化合物偏移31-60 nm.P1和P2(CHC13溶液)分别在〜515 nm和〜560 nm处观察到最大发射峰。 -掺杂。

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