Literature DB >> 23736953

Rigid organic nanotubes obtained from phenylene-butadiynylene macrocycles.

Simon Rondeau-Gagné1, Jules Roméo Néabo, Maude Desroches, Isabelle Levesque, Maxime Daigle, Katy Cantin, Jean-François Morin.   

Abstract

Rigid organic nanotubes were prepared from six-membered phenylene-butadiynylene macrocycles through topochemical polymerization in the xerogel state. All six butadiyne units underwent polymerization, thus creating rigid nanotubes with six polydiacetylene chains lying parallel, one relative to each other.

Entities:  

Year:  2013        PMID: 23736953     DOI: 10.1039/c3cc43177k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  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

  1 in total

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