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

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 re...

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Veröffentlicht in:Beilstein journal of organic chemistry 2014-07, Vol.10 (1), p.1613-1619
Hauptverfasser: Rondeau-Gagné, Simon, Néabo, Jules Roméo, Daigle, Maxime, Cantin, Katy, Morin, Jean-François
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Sprache:eng
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Zusammenfassung: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).
ISSN:1860-5397
1860-5397
DOI:10.3762/bjoc.10.167