TADF Sensitizer and Hot-Exciton Emitter: The conventional host molecule undergoes a conversion into a TADF sensitizer and a Hot-Exciton emitter via distinct donor and acceptor unit substitutions on the adamantane core. Molecules incorporat...
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5‐Aryl Substituted 2‐(2‐Methoxyphenyl)benzoxazoles with Large Stokes Shifts: Synthesis, Crystal Structures and Optical Properties
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Unlike 2-(2-hydroxyphenyl)benzoxales (HBOs), 2-(2-methoxyphenyl)benzoxazoles (MBOs) lack the sought-after large Stokes shifts of the former which are necessary in fluorescence microscopy. Herein, we demonstrate that the 5-aryl substitution of MBOs affords 2-(4-methoxy-[1,1’-biphenyl]-3-yl)benzoxazoles (MBBOs) dyes with large Stokes shifts.
Abstract
2-(2-methoxyphenyl)benzoxazole (MBO) displays similar photophysical properties to 2-(2-hydroxyphenyl)benzoxazole (HBO), but it lacks the large Stokes shifts necessary for fluorescence microscopy applications. In this paper, we report the 5-substitution of MBO with aryl groups to produce 2-(4-methoxy-[1,1’-biphenyl]-3-yl)benzoxazoles (MBBOs) with large Stokes shifts. The synthesis of MBBOs 6–15 was accomplished in moderate to good yields by microwave-assisted Sonogashira cross couplings. Crystal structures for compounds 6–9 and 15 are provided. MBBOs 6–10, 12, and 14 displayed considerably blue-shifted absorption maxima and slight bathochromic shifts of their fluorescence maxima relative to the unsubstituted MBO.
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