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

Authors :
Simon Rondeau-Gagné
Jules Roméo Néabo
Maxime Daigle
Katy Cantin
Jean-François Morin
Source :
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1613-1619 (2014)
Publication Year :
2014
Publisher :
Beilstein-Institut, 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).

Details

Language :
English
ISSN :
18605397
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Beilstein Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.63684583b944fc18e659e7afde2996b
Document Type :
article
Full Text :
https://doi.org/10.3762/bjoc.10.167