Abstract
This Article describes the design, synthesis, and analysis of a new class of polymer that is capable of depolymerizing continuously, completely, and cleanly from head to tail when a detection unit on the head of the polymer is exposed to a specific applied signal. The backbone of this polymer consists of 1,3-disubstituted pyrroles and carboxy linkages similar to polyurethanes. Diverse side chains or reactive end-groups can be introduced readily, which provides modular design of polymer structure. The designed depolymerization mechanism proceeds through spontaneous release of carbon dioxide and azafulvene in response to a single triggering reaction with the detection unit. These poly(carboxypyrrole)s depolymerize readily in nonpolar environments, and even in the bulk as solid-state plastics.
| Original language | American English |
|---|---|
| Pages (from-to) | 9447-9452 |
| Number of pages | 6 |
| Journal | Journal of the American Chemical Society |
| Volume | 142 |
| Issue number | 20 |
| DOIs | |
| State | Published - 20 May 2020 |
Keywords
- depolymerization
- gel permeation chromatography
- oxides
- polymers
- pyrroles
EGS Disciplines
- Materials Science and Engineering
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