Meso-Substitution Controlled Synthesis of BODIPY–DPM Conjugates: A Pathway to Tailored Photophysical Properties

Sonia Swami; Harshita Saroj; Ritika Jaiswal; Yohei Adachi; Aniruddha Roy; Joji Ohshita; P. Arora; Nitika Grover

doi:10.1039/d6cc01186a

January 1, 2026Chemical Communications

Meso-Substitution Controlled Synthesis of BODIPY–DPM Conjugates: A Pathway to Tailored Photophysical Properties

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Key Points

To explore how meso-substituent control affects the synthesis and properties of BODIPY-DPM conjugates.
Controlled synthesis of BODIPY-DPM conjugates
Investigation of mono- and bis-condensation reactions
Characterization of photophysical properties
Conjugates show deep-red absorption
Exhibit efficient triplet formation
High singlet-oxygen generation observed

Implication

Meso-substituent-controlled reactivity enhances absorption and singlet-oxygen in BODIPY-DPM conjugates, indicating improved photophysical properties.

Abstract

Meso-Substituent-controlled reactivity in meso-aryl-1,3,5,7-tetramethyl BODIPY facilitates selective mono- or bis-condensation with pyrrole-2-aldehyde or 1,9-diformyl-dipyrromethanes. The resulting π-extended BODIPY-DPM/pyrrole conjugates exhibit deep-red absorption, NIR emission, efficient triplet formation, and high singlet-oxygen...

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Cite This Study

Swami et al. (2026) studied this question.

synapsesocial.com/papers/69faa30204f884e66b533acb https://doi.org/10.1039/d6cc01186a

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Meso-Substitution Controlled Synthesis of BODIPY–DPM Conjugates: A Pathway to Tailored Photophysical Properties

Key Points

Implication

Abstract

Discussion

Cite This Study

Meso-Substitution Controlled Synthesis of BODIPY–DPM Conjugates: A Pathway to Tailored Photophysical Properties

Key Points

Implication

Abstract

Discussion

Cite This Study

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