Abstract
A simple modular strategy for the synthesis of profluorescent nitroxide containing polymers is described. The incorporation of an epoxide as a pendant functionality on a polymer backbone synthesized using ATRP and subsequent nucleophilic ring-opening with sodium azide gave hydroxyl and azide functionality within a 3-bond radius. Orthogonal coupling chemistry then allowed the independent attachment of fluorophore and nitroxide groups in close proximity, giving rise to a profluorescent polymer. Validation of the viability of these materials as fluorescent sensors is demonstrated through efficient fluorescence switch-on observed when the materials are exposed to a model reductant or carbon-centred radical source. This journal is
| Original language | English |
|---|---|
| Pages (from-to) | 2962-2969 |
| Journal | Polymer Chemistry |
| Volume | 6 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 21 Apr 2015 |
| Externally published | Yes |
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