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Synthesis and Structural Diversification of Circularly Polarised Luminescence Active, Helically Chiral, “Confused” <i>N</i>,<i>N</i>,<i>O</i>,<i>C</i>‐BODIPYs**

Rebecca G. Clarke, Jake Weatherston, Rafid A. Taj‐Aldeen, Paul G. Waddell, William McFarlane, Thomas J. Penfold, Jonathan Bogaerts, Wouter Herrebout, Lewis E. MacKenzie, Róbert Pál, Michael J. Hall

2022ChemPhotoChem13 citationsDOIOpen Access PDF

Abstract

Abstract Helically chiral boron‐chelated dipyrromethene (BODIPY) dyes are known to exhibit solution phase circularly polarized luminescence (CPL), but examples are limited to a few synthetically accessible molecular architectures. We report a B−N chelation, S N Ar, Suzuki cross‐coupling, B−O chelation cascade reaction for the synthesis of understudied helically chiral, N , N , O , C ‐boron chelated, “confused” BODIPYs, from readily accessible 3,5‐dibromo‐BODIPY starting materials. Using this approach we have prepared a series of helically chiral “confused” BODIPYs with variation of the 3,5‐subsitutents. Following resolution by chiral HPLC, absolute stereochemistry was assigned through comparison of the experimental and calculated ECD spectra, and solution phase chiroptical properties including CPL were determined (| g lum | from 2.1 to 3.7×10 −3 ; B CPL from 11.3 to 27.2).

Topics & Concepts

BODIPYChelationLuminescenceBoronChemistryCircular dichroismStereochemistryCrystallographyMaterials scienceOrganic chemistryPhysicsFluorescenceOpticsOptoelectronicsLuminescence and Fluorescent MaterialsSynthesis and Properties of Aromatic CompoundsMolecular Sensors and Ion Detection
Synthesis and Structural Diversification of Circularly Polarised Luminescence Active, Helically Chiral, “Confused” <i>N</i>,<i>N</i>,<i>O</i>,<i>C</i>‐BODIPYs** | Litcius