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.
| Original language | English |
|---|---|
| Pages (from-to) | 12301-12306 |
| Number of pages | 6 |
| Journal | Chemistry - A European Journal |
| Volume | 22 |
| Issue number | 35 |
| DOIs | |
| State | Published - Aug 22 2016 |
Keywords
- azide–alkyne cycloaddition
- pi interactions
- polymerization
- supramolecular chemistry
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