| Literature DB >> 27338246 |
Xisen Hou1, Chenfeng Ke2, Yu Zhou3, Zhuang Xie1, Ahmed Alngadh4, Denis T Keane3, Majed S Nassar4, Youssry Y Botros4, Chad A Mirkin1,3, J Fraser Stoddart5.
Abstract
Covalent and supramolecular polymerizations, both of which offer their own unique advantages, have emerged as popular strategies for making artificial materials. Herein, we describe a concurrent covalent and supramolecular polymerization strategy-namely, one which utilizes 1) a bis-azide-functionalized diazaperopyrenium dication that undergoes polymeriation covalently with a bis-alkyne-functionalized biphenyl derivative in one dimension as a result of a rapid and efficient β-cyclodextrin(CD)-accelerated, cucurbit[6]uril(CB)-templated azide-alkyne cycloaddition, while 2) the aromatic core of the dication is able to dimerize in a criss-cross fashion by dint of π-π interactions, enabling simultaneous supramolecular assembly, resulting in an extended polymer network in an orthogonal dimension.Keywords: azide-alkyne cycloaddition; pi interactions; polymerization; supramolecular chemistry
Year: 2016 PMID: 27338246 DOI: 10.1002/chem.201602954
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236