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首页> 外文期刊>RSC Advances >New synthetic strategy targeting well-defined α,ω-telechelic polymethylenes with hetero bi-/tri-functionalities via polyhomologation of ylides initiated by new organic boranes based on catecholborane and post functionalization
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New synthetic strategy targeting well-defined α,ω-telechelic polymethylenes with hetero bi-/tri-functionalities via polyhomologation of ylides initiated by new organic boranes based on catecholborane and post functionalization

机译:通过基于儿茶酚硼烷和后官能化的新的有机硼化物引发的yliders的多溴化物,靶向具有杂双/三官能度的杂α,ω-Trecelicites的新的合成策略。

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A series of well-defined α,ω-telechelic polymethylenes with hetero bi-/tri-functionalities were synthesized by a tandem strategy combining polyhomologation of ylides initiated by new organic boranes based on catecholborane with post functionalization using end-capping reagents and esterification. The chain structures of such polymers were attested by ~(1) H NMR spectra, FT-IR and GPC. The functionality can reach up to 100%, and the molecular weights of the obtained polymers showed a range from 870 to 12?080 g mol ~(?1) with a narrow distribution ( ? = 1.04–1.12).
机译:通过基于儿茶酚硼烷基因的圆形硼烷和酯化后官能化和酯化,通过将基于儿茶酚酰胺的多溴化物的串联策略组合的串联策略合成了具有杂双/三官能度的一系列具有杂双/三函数的α,ω-遥联甲基。通过〜(1)H NMR光谱,FT-IR和GPC检测这种聚合物的链结构。该功能可达100%,所得聚合物的分子量显示为870至12μl080gmol〜(Δ1)的范围,分布窄(?= 1.04-1.12)。

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