TY - JOUR
T1 - Fluorescence pH Probes Based on Photoinduced Electron Transfer Quenching of Long Fluorescence Lifetime Triangulenium Dyes
AU - Rosenberg, Martin
AU - Junker, Anne Kathrine R.
AU - Sørensen, Thomas Just
AU - Laursen, Bo W.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Azaoxatriangulenium dyes with long fluorescence lifetimes offer advantages in fluorescence lifetime imaging (FLIM), time-gated detection and polarization assays. However, the long excited state lifetimes are also expected to increase sensitivity to photoinduced electron transfer (PET) quenching, potentially increasing the on-off ratio of PET probes. We report the synthesis and investigation of the optical properties of azaoxatriangulenium salts substituted with phenol substituents for pH sensing. Two series of pH probes with the phenol hydroxy group placed in the ortho, meta, or para positions to azadioxatriangulenium (ADOTA) and diazaoxatriangulenium (DAOTA) chromophores are investigated. All the phenol-substituted dyes possess pH-responsive fluorescence signals in the biologically relevant pH window (pH 6–9) due to efficient intramolecular PET from the phenolate form of the pendant arm. While the PET mechanism is partly suppressed in the phenol form of the ADOTA derivatives, it is completely suppressed in the DAOTA derivatives. The long excited state lifetimes of the triangulenium dyes ensure efficient PET quenching leading to very high on-off ratios of the pH probes. The study clearly demonstrates effects of the position of the phenol/phenolate group relative to the chromophore on both PET quenching rates and pKa values.
AB - Azaoxatriangulenium dyes with long fluorescence lifetimes offer advantages in fluorescence lifetime imaging (FLIM), time-gated detection and polarization assays. However, the long excited state lifetimes are also expected to increase sensitivity to photoinduced electron transfer (PET) quenching, potentially increasing the on-off ratio of PET probes. We report the synthesis and investigation of the optical properties of azaoxatriangulenium salts substituted with phenol substituents for pH sensing. Two series of pH probes with the phenol hydroxy group placed in the ortho, meta, or para positions to azadioxatriangulenium (ADOTA) and diazaoxatriangulenium (DAOTA) chromophores are investigated. All the phenol-substituted dyes possess pH-responsive fluorescence signals in the biologically relevant pH window (pH 6–9) due to efficient intramolecular PET from the phenolate form of the pendant arm. While the PET mechanism is partly suppressed in the phenol form of the ADOTA derivatives, it is completely suppressed in the DAOTA derivatives. The long excited state lifetimes of the triangulenium dyes ensure efficient PET quenching leading to very high on-off ratios of the pH probes. The study clearly demonstrates effects of the position of the phenol/phenolate group relative to the chromophore on both PET quenching rates and pKa values.
U2 - 10.1002/cptc.201800266
DO - 10.1002/cptc.201800266
M3 - Journal article
SN - 2367-0932
VL - 3
SP - 233
EP - 242
JO - ChemPhotoChem
JF - ChemPhotoChem
IS - 5
ER -