Pushing the Boundaries of BODIPY Chemistry: 2-(Dimethylamino)methyl BODIPYs as Enablers of Diversification with Nucleophiles

Sergio Serrano; Carla Marcos; Natalia Casado; Andrea Aranda; Florencio Moreno Jiménez; Jorge Bañuelos; David Valdivieso González; Iván López‐Montero; Beatriz Lora Maroto; Santiago De la Moya

doi:10.1039/d5sc08677a

January 1, 2026Chemical ScienceOpen Access

Pushing the Boundaries of BODIPY Chemistry: 2-(Dimethylamino)methyl BODIPYs as Enablers of Diversification with Nucleophiles

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Key Points

The study aims to expand the utility of BODIPY dyes through the introduction of nucleophiles for enhanced functionalization.
Investigated the photophysical properties of BODIPY compounds.
Explored post-functionalization reactions with various nucleophiles.
Assessed the synthetic routes for generating diverse BODIPY derivatives.
Demonstrated successful diversification of BODIPY dyes using nucleophiles.
Showed enhanced photophysical properties across newly formed compounds.
Highlighted the versatility of BODIPY derivatives in potential applications.

Implication

Exploration of BODIPY chemistry enables diversification with nucleophiles, suggesting new possibilities in photonic materials.

Abstract

The BODIPY family of organic dyes has emerged as a versatile platform in photonic materials science, driven by their outstanding photophysical properties and the synthetic flexibility of BODIPY chemistry. Post-functionalization...

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Cite This Study

Serrano et al. (2026) studied this question.

synapsesocial.com/papers/698c1d1d267fb587c655fa32 https://doi.org/10.1039/d5sc08677a

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Pushing the Boundaries of BODIPY Chemistry: 2-(Dimethylamino)methyl BODIPYs as Enablers of Diversification with Nucleophiles

Key Points

Implication

Abstract

Discussion

Cite This Study

Pushing the Boundaries of BODIPY Chemistry: 2-(Dimethylamino)methyl BODIPYs as Enablers of Diversification with Nucleophiles

Key Points

Implication

Abstract

Discussion

Cite This Study

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