BINOL blocks as accessible triplet state modulators in BODIPY dyes

Jiménez, Josué; Prieto-Montero, Ruth; Serrano, Sergio; Stachelek, Patrycja; Rebollar, Esther; Maroto, Beatriz L.; Moreno, Florencio; Martinez-Martinez, Virginia; Pal, Robert; García-Moreno, Inmaculada; de la Moya, Santiago

Abstract

BINOL moieties of different electronic demand are useful blocks for enabling the photo-production and modulation of triplet excited states in readily-accesible BINOL-based O-BODIPY dyes from standard F-BODIPY precursors. The rapid and rational development of smarter triplet-enabling BODIPY dyes on the basis of this strategy (e.g., TADF biomarker 4a or room temperature phosphor 4g) paves the way for advancing photonic applications based on organic triplet photosensitizers.

Citation

Jiménez, J., Prieto-Montero, R., Serrano, S., Stachelek, P., Rebollar, E., Maroto, B. L., Moreno, F., Martinez-Martinez, V., Pal, R., García-Moreno, I., & de la Moya, S. (2022). BINOL blocks as accessible triplet state modulators in BODIPY dyes. Chemical Communications, 58(44), 6385-6388. https://doi.org/10.1039/d2cc00991a

• Journal Article Type: Article
• Acceptance Date: May 4, 2022
• Online Publication Date: May 4, 2022
• Publication Date: Jun 4, 2022
• Deposit Date: Jun 30, 2022
• Publicly Available Date: May 4, 2023
• Journal: Chemical Communications
• Print ISSN: 1359-7345
• Electronic ISSN: 1364-548X
• Publisher: Royal Society of Chemistry
• Peer Reviewed: Peer Reviewed
• Volume: 58
• Issue: 44
• Pages: 6385-6388
• DOI: https://doi.org/10.1039/d2cc00991a
• Public URL: https://durham-repository.worktribe.com/output/1200831