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Deprotection of a benzyl unit induces a 22 pi aromatic macrocycle of 3-oxypyripentaphyrin(0.1.1.1.0) with strong NIR absorption

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/82294

Title: Deprotection of a benzyl unit induces a 22 pi aromatic macrocycle of 3-oxypyripentaphyrin(0.1.1.1.0) with strong NIR absorption
Authors: Mori, Daiki Browse this author
Yoneda, Tomoki Browse this author →KAKEN DB
Suzuki, Masaaki Browse this author
Hoshino, Tyuji Browse this author
Neya, Saburo Browse this author
Issue Date: 28-Jul-2020
Publisher: Royal Society of Chemistry
Journal Title: Organic & biomolecular chemistry
Volume: 18
Issue: 28
Start Page: 5334
End Page: 5338
Publisher DOI: 10.1039/d0ob01213k
Abstract: We report aromaticity switching from a 6 pi pyridine ring to a 22 pi macrocyclic ring of 3-oxypyripentaphyrin(0.1.1.1.0). This system has potential applications in photodynamic therapy owing to macrocyclic aromaticity being selectively induced by protecting group removal and strong absorption bands produced in the NIR region especially in methanol.
Type: article (author version)
URI: http://hdl.handle.net/2115/82294
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 米田 友貴

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