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Dual emissive properties of solid-state difluoroboron β-diketonate-poly(lactic acid) (BF 2 bdk-PLA) materials have been utilized as biological oxygen sensors. Dyes with red-shifted absorption and emission are important for multiplexing and in vivo imaging, thus hydroxyl-functionalized dinaphthoylmethane initiators and dye-PLA conjugates BF 2 dnm(X)PLA (X = H, Br, I) with extended conjugation were synthesized. The luminescent materials show red-shifted absorbance (∼435 nm) and fluorescence tunability by molecular weight. Fluorescence colors range from yellow (∼530 nm) in 10–12 kDa polymers to green (∼490 nm) in 20–30 kDa polymers. Room-temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF) are present under a nitrogen atmosphere. For the iodine-substituted derivative, BF 2 dnm(I)PLA, clearly distinguishable fluorescence (green) and phosphorescence (orange) peaks are present, making it ideal for ratiometric oxygen-sensing and imaging. Bromide and hydrogen analogues with weaker relative phosphorescence intensities and longer phosphorescence lifetimes can be used as highly sensitive, concentration independent, lifetime-based oxygen sensors or for gated emission detection. BF 2 dnm(I)PLA nanoparticles were taken up by T41 mouse mammary cells and successfully detected differences in oxygen levels during in vitro ratiometric imaging.
DeRosa et al. (Thu,) studied this question.