Literature DB >> 21556417

H-bonding-driven gel formation of a phenylacetylene macrocycle.

Katy Cantin1, Simon Rondeau-Gagné, Jules Roméo Néabo, Maxime Daigle, Jean-Francois Morin.   

Abstract

An amide-containing phenylacetylene macrocycle (PAM) has been synthesized and its gelation properties were studied in different solvents. Surprisingly, this macrocycle forms organogels at low concentration in many polar and apolar solvents. XRD and FTIR analysis suggest that this macrocycle forms stable supramolecular assemblies owing to H-bonding. Scanning electron microscopy analyses show the formation of bundles of nanofibrils, demonstrating the long-range organization of this material.

Entities:  

Year:  2011        PMID: 21556417     DOI: 10.1039/c1ob05441d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  The influence of intraannular templates on the liquid crystallinity of shape-persistent macrocycles.

Authors:  Joscha Vollmeyer; Ute Baumeister; Sigurd Höger
Journal:  Beilstein J Org Chem       Date:  2014-04-23       Impact factor: 2.883

2.  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
Journal:  Beilstein J Org Chem       Date:  2014-07-15       Impact factor: 2.883

  2 in total

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