Heteroatom-Functionalization of Aromatic Rings Using Near Infrared Light-Activatable Catalysts

The development of molecular transformation reactions driven by highly penetrating near-infrared (NIR) light presents a promising platform for organic synthesis. Here, we report a reaction that allows the heteroatom-functionalization of aromatic rings using a phthalocyanine-based NIR photocatalyst. The use of phthalocyanine zinc complexes capable of generating singlet oxygen (<sup>1</sup>O<sub>2</sub>) upon NIR irradiation was investigated, focusing on the generation of aryl radicals by the reaction of arylhydrazine derivatives with <sup>1</sup>O<sub>2</sub>. Arylhydrazine hydrochloride, a precursor that is stable and easy to handle, enabled the incorporation of various heteroatoms, including P, S, and B, onto the aromatic ring through electrophilic/nucleophilic trapping with aryl radicals. This methodology enables the selective transformation of fluorescent dyes and facilitates reactions even under shielded conditions, which are often challenging with conventional photochemical reactions. Thus, our strategy offers a novel approach to the functionalization of aromatic rings using NIR light.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-02-18
DOI
https://doi.org/10.1021/acs.joc.5c02598
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Heteroatom-Functionalization of Aromatic Rings Using Near Infrared Light-Activatable Catalysts

Taniyuki Furuyama, Rinko Kobayashi, Tasuku Iba
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Heteroatom-Functionalization of Aromatic Rings Using Near Infrared Light-Activatable Catalysts

Taniyuki Furuyama, Rinko Kobayashi, Tasuku Iba
article en

Abstract

The development of molecular transformation reactions driven by highly penetrating near-infrared (NIR) light presents a promising platform for organic synthesis. Here, we report a reaction that allows the heteroatom-functionalization of aromatic rings using a phthalocyanine-based NIR photocatalyst. The use of phthalocyanine zinc complexes capable of generating singlet oxygen (<sup>1</sup>O<sub>2</sub>) upon NIR irradiation was investigated, focusing on the generation of aryl radicals by the reaction of arylhydrazine derivatives with <sup>1</sup>O<sub>2</sub>. Arylhydrazine hydrochloride, a precursor that is stable and easy to handle, enabled the incorporation of various heteroatoms, including P, S, and B, onto the aromatic ring through electrophilic/nucleophilic trapping with aryl radicals. This methodology enables the selective transformation of fluorescent dyes and facilitates reactions even under shielded conditions, which are often challenging with conventional photochemical reactions. Thus, our strategy offers a novel approach to the functionalization of aromatic rings using NIR light.

The Journal of Organic Chemistry
Kanazawa University (JP), University of Hyogo (JP)
Openalex Percentile: Top 49%
Radical Photochemical Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.