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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

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Josué Jiménez

Ruth Prieto-Montero

Sergio Serrano

Patrycja Stachelek

Esther Rebollar

Beatriz L. Maroto

Florencio Moreno

Virginia Martinez-Martinez

Inmaculada García-Moreno

Santiago de la Moya


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.


Jiménez, J., Prieto-Montero, R., Serrano, S., Stachelek, P., Rebollar, E., Maroto, B. L., …de la Moya, S. (2022). BINOL blocks as accessible triplet state modulators in BODIPY dyes. Chemical Communications, 58(44), 6385-6388.

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


Accepted Journal Article (Supporting Information) (1.3 Mb)

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