Unconventional
fluorescent polymers have attracted increasing attention
due to their simple preparation, good biocompatibility, and stable
photophysical properties. Polyglycidol-acrylates (PGL-acrylates) with
tunable multicolor emission were prepared by one-pot in this study.
First, PGL was synthesized by the ring-opening polymerization of glycidol,
and then the terminal hydroxyl groups in polyglycidol were modified
using propiolic acid ester via the oxa-Michael reaction in situ, forming
PGL-acrylates with terminal acrylate units. The fluorescence emission
of PGL-acrylate follows the clustering-triggered emission (CTE) mechanism,
where the through-space interaction (TSI) between the acrylate units
forms the clusters. All of the prepared PGL-acrylates show typical
concentration-enhanced emission and excitation-dependent emission,
and significant emission at 640 nm was observed. Particularly, PGL-acrylate
demonstrated an unusual concentration-excitation-dependent emission
(EDE) behavior, in which the maximum excitation and emission wavelengths
of the solution showed considerable red-shift with the increased PGL-acrylate
concentration. This could come from the increased π–π*
interactions with increased double-bond concentration, which stack
and drive a more compact structure of the luminescent clusters. The
compact cluster structure enhances the TSI effect and expands the
delocalized electrons, leading to increased emission and red-shift.
As the steric hindrance of the terminal methyl acrylate unit increases,
it is difficult to form a more compact cluster structure, and the
fluorescence emission is blue-shifted. PGL-acrylate also has low cytotoxicity
and good cell imaging ability and is expected to be used in biomedical
applications.