Abstract
The synthesis of thiolactone monomers that mimic natural nucleosides and engage in robust ring opening polymerizations (ROP) is herein described. As each repeat unit contains a thioester functional group, dynamic rearrangement of the polymer is feasible via thiol-thioester exchange, demonstrated here by depolymerization of the polymers and coalescing of two polymers of different molecular weight or chemical composition. This approach constitutes the first step toward a platform that enables for the routine synthesis of sequence controlled polymers via dynamic template directed synthesis.
| Original language | English |
|---|---|
| Pages (from-to) | 13594-13598 |
| Number of pages | 5 |
| Journal | Journal of the American Chemical Society |
| Volume | 140 |
| Issue number | 42 |
| DOIs | |
| State | Published - 24 Oct 2018 |
| Externally published | Yes |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry