Abstract
Suzuki cross-coupling polymerisation of aryldibromides and aryldiboronate esters in a sodium dodecyl sulfate (SDS)-stabilised miniemulsion provides a versatile and direct route to fluorescent conjugated polymer nanoparticles (CPNs). These nanoparticles have a conjugated backbone based on poly(9,9-dioctylfluorene) (PFO), however, significant structural diversity is introduced by incorporation of electron withdrawing, heterocyclic comonomers (5–50 mol.%) in order to tune the emission wavelengths from blue to far-red/near-infrared. The robust nature of the polymerisation methodology allows for rapid assessment of the relationship between polymer composition, chain morphology and optical properties of the resultant CPNs. Moreover, the CPNs (after a simple and rapid purification step) can be used directly in fluorescence-based intracellular labelling experiments (in HCT116 cells), in which they display low cytotoxicity at biologically-useful concentrations.
| Original language | English |
|---|---|
| Pages (from-to) | 69-77 |
| Journal | Reactive and Functional Polymers |
| Volume | 107 |
| Early online date | 30 Aug 2016 |
| DOIs | |
| Publication status | Published - 1 Oct 2016 |
Keywords
- conjugated polymer nanoparticles
- miniemulsion
- Suzuki-Miyaura polymerisation
- scaleable
- bioimaging
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