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Retro Diels-Alder-triggered self-assembly of a polymerizable macrocyclic diacetylene

A new triggered self-assembly method, which utilizes retro Diels-Alder (rDA)-promoted self-assembly of a macrocyclic diacetylene, was developed. The steric bulk present in a Diels-Alder (DA) adduct was released by a thermally promoted rDA reaction, resulting in the generation of a linear diacetylene...

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Bibliographic Details
Published in:Organic & biomolecular chemistry 2023-08, Vol.21 (31), p.632-636
Main Authors: Heo, Jung-Moo, Park, Jaeyoung, Kim, Jong-Man
Format: Article
Language:English
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Summary:A new triggered self-assembly method, which utilizes retro Diels-Alder (rDA)-promoted self-assembly of a macrocyclic diacetylene, was developed. The steric bulk present in a Diels-Alder (DA) adduct was released by a thermally promoted rDA reaction, resulting in the generation of a linear diacetylene that readily self-assembles to form a supramolecular polymer. The maleimide-containing blue-colored polydiacetylene, which was generated by UV irradiation, was utilized as a thiol specific colorimetric sensor. A new triggered self-assembly (SA) method, which utilizes retro Diels-Alder (rDA)-promoted self-assembly of a macrocyclic diacetylene, was developed.
ISSN:1477-0520
1477-0539
DOI:10.1039/d3ob00953j