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通过侧链修饰提高苯乙炔大环的立体聚合反应性。

Improving the reactivity of phenylacetylene macrocycles toward topochemical polymerization by side chains modification.

机构信息

Département de Chimie and Centre de recherche sur les Matériaux Avancés (CERMA), Université Laval, 1045 avenue de la Médecine, G1V 0A6 Québec, Québec, Canada.

出版信息

Beilstein J Org Chem. 2014 Jul 15;10:1613-1619. doi: 10.3762/bjoc.10.167. eCollection 2014.

Abstract

The synthesis and self-assembly of two new phenylacetylene macrocycle (PAM) organogelators were performed. Polar 2-hydroxyethoxy side chains were incorporated in the inner part of the macrocycles to modify the assembly mode in the gel state. With this modification, it was possible to increase the reactivity of the macrocycles in the xerogel state to form polydiacetylenes (PDAs), leading to a significant enhancement of the polymerization yields. The organogels and the PDAs were characterized using Raman spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM).

摘要

进行了两个新的苯乙炔大环(PAM)有机凝胶剂的合成和自组装。极性 2-羟乙氧基侧链被引入大环的内部,以修饰在凝胶状态下的组装方式。通过这种修饰,可以增加在干凝胶状态下大环的反应性,形成聚二乙酰基(PDAs),从而显著提高聚合产率。使用拉曼光谱、X 射线衍射(XRD)和扫描电子显微镜(SEM)对有机凝胶和 PDAs 进行了表征。

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