A borindolizine platform for the design of fluorophores with tunable emissions
Here we describe the design and applications of borindolizine, a novel scaffold with broadly tunable fluorescence and a high Stokes shift. Two classes of emitters were synthesized through rational scaffold modification, resulting in blue-emitting carboxyborindolizines (<i>λ</i> <sub>max,em</sub> = 431-459 nm) and green-emitting aryl borindolizines (<i>λ</i> <sub>max,em</sub> = 489-519 nm). Experimental structure-emission trends were used to validate a computational spectral prediction model and to subsequently design a red-emissive borindolizine scaffold. The red-emissive isoquinolyl borinidolizine was prepared, and the experimental emission (<i>λ</i> <sub>max,abs</sub> = 370 nm, <i>λ</i> <sub>max,em</sub> = 635 nm) was in excellent agreement with the theoretical emission (<i>λ</i> <sub>max,em</sub> = 646 nm). These results show how the application of data science can produce fluorophores with desirable spectroscopic properties through the borindolizine scaffold.
Authors
- Adam Marr
- Nicholas W. Heller (ORCID: https://orcid.org/0009-0004-0892-4256)
- Alán Aspuru‐Guzik (ORCID: https://orcid.org/0000-0002-8277-4434)
- Andrei K. Yudin (ORCID: https://orcid.org/0000-0003-3170-9103)
- Kjell Jorner (ORCID: https://orcid.org/0000-0002-4191-6790)
- Chirag Apte (ORCID: https://orcid.org/0000-0002-0108-8580)
- Ben Zhen Huang
Institutions
- University of Toronto (CA)
- Chalmers University of Technology (SE)
Publication Details
- Journal
- Chemical Science
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5sc04328j
- Citations
- 1
- Primary Topic
- Synthesis and Reactivity of Heterocycles
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- Natural Sciences and Engineering Research Council of Canada