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Methoxy‐Substituted Difluoroboron Benzoylacetonate Complexes with Color‐Tunable Phosphorescence
Author(s) -
DeRosa Christopher A.,
Daly Margaret L.,
Kerr Caroline,
Fraser Cassandra L.
Publication year - 2019
Publication title -
chemphotochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.13
H-Index - 18
ISSN - 2367-0932
DOI - 10.1002/cptc.201800156
Subject(s) - phosphorescence , fluorescence , substituent , photochemistry , absorbance , density functional theory , benzene , chemistry , materials science , organic chemistry , optics , computational chemistry , physics , chromatography
Difluoroboron β‐diketonates (BF 2 bdks) exhibit fluorescence (F) and room‐temperature phosphorescence (RTP) in a poly(lactic acid) (PLA) matrix. Fluorescence color tuning has been achieved by dye loading or bdk ligand modification, namely substituent effects or extended conjugation. In this study, color‐tunable RTP (450–570 nm) is achieved with 1‐benzoylacetonate derivatives by varying the number and position of methoxy groups on the benzene ring. The methoxy groups can be used to alter the energy levels of the dye or induce geometry changes (e. g. twisting) to disrupt π‐conjugation. The dyes were evaluated theoretically with density functional theory (DFT) and spectroscopy (absorbance and fluorescence) in CH 2 Cl 2 solution and dilute PLA blends. These findings inform future boron‐based lighting devices and oxygen‐sensing bioprobe designs.

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