N-Pechmann aza-BODIPYs: enhanced near-infrared photothermal conversion by the cross-conjugated structure

Yuma Tanaka; Yuya Taninokuchi; Taichi Sawamura; Saori Okamura; Shigeki Mori; Masatoshi Ishida; Koji Miki; Kouichi Ohe; Takanori Iwasaki; Soji Shimizu

doi:10.1039/d6qo00024j

January 1, 2026Organic Chemistry Frontiers

N-Pechmann aza-BODIPYs: enhanced near-infrared photothermal conversion by the cross-conjugated structure

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Key Points

Investigate the photothermal conversion efficiency of NPAB-55, a dimeric aza-BODIPY analogue.
Synthesize dimeric aza-BODIPY analogue NPAB-55.
Analyze photothermal conversion properties using near-infrared light.
Evaluate thermal decay processes from excited states.
NPAB-55 shows enhanced near-infrared photothermal conversion compared to previous models.
The cross-conjugated structure promotes efficient thermal decay from excited states.

Implication

Dimeric aza-BODIPY NPAB-55 improves photothermal conversion in a cross-conjugated structure, suggesting significant applications.

Abstract

Near-infrared (NIR) photothermal (PT) conversion was achieved with the dimeric aza-BODIPY analogue called NPAB-55, comprising a cross-conjugated, exocyclic double bond for enhancing thermal decay processes from the excited states. NPAB-55...

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Cite This Study

Tanaka et al. (2026) studied this question.

synapsesocial.com/papers/6996a818ecb39a600b3ee7ff https://doi.org/10.1039/d6qo00024j

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N-Pechmann aza-BODIPYs: enhanced near-infrared photothermal conversion by the cross-conjugated structure

Key Points

Implication

Abstract

Discussion

Cite This Study

N-Pechmann aza-BODIPYs: enhanced near-infrared photothermal conversion by the cross-conjugated structure

Key Points

Implication

Abstract

Discussion

Cite This Study

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