Abstract
We designed 2,6-bis(hydroxymethyl)anilines bearing protecting groups sensitive to UV light, acid, or base, and used the protected anilines as co-monomers for the synthesis of trigger-responsive polymers. The resulting polymers underwent chain-shattering degradation once the protecting groups were removed, which could be used for trigger-responsive burst release applications. This journal is
| Original language | English (US) |
|---|---|
| Pages (from-to) | 224-228 |
| Number of pages | 5 |
| Journal | Polymer Chemistry |
| Volume | 4 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 21 2013 |
ASJC Scopus subject areas
- Bioengineering
- Biochemistry
- Polymers and Plastics
- Organic Chemistry