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  1. Academic Journal articles
  2. Narita Unit

Synthesis of Bioctacene‐Incorporated Nanographene with Near‐Infrared Chiroptical Properties

https://oist.repo.nii.ac.jp/records/2000273
https://oist.repo.nii.ac.jp/records/2000273
b1ea9127-8254-4e53-a77d-a60fa2c3ecfa
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Angew Angew Chem Int Ed - 2023 - Xu - Synthesis of B.pdf (1.1 MB)
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Item type 学術雑誌論文 / Journal Article(1)
PubDate 2023-11-29
Title
Title Synthesis of Bioctacene‐Incorporated Nanographene with Near‐Infrared Chiroptical Properties
Language en
Language
Language eng
Keyword
Language en
Subject Scheme Other
Subject Chirality | Fjord-Edge | Nanographene | Near-Infrared | Zigzag-Edge
Resource Type
Resource Type Identifier http://purl.org/coar/resource_type/c_6501
Resource Type journal article
Access Right
Access Rights open access
Access Rights URI http://purl.org/coar/access_right/c_abf2
Author Xu, Xiushang

× Xu, Xiushang

en Xu, Xiushang

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Muñoz‐Mármol, Rafael

× Muñoz‐Mármol, Rafael

en Muñoz‐Mármol, Rafael

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Vasylevskyi, Serhii

× Vasylevskyi, Serhii

en Vasylevskyi, Serhii

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Villa, Andrea

× Villa, Andrea

en Villa, Andrea

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Folpini, Giulia

× Folpini, Giulia

en Folpini, Giulia

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Scotognella, Francesco

× Scotognella, Francesco

en Scotognella, Francesco

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Maria Paternò, Giuseppe

× Maria Paternò, Giuseppe

en Maria Paternò, Giuseppe

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Narita, Akimitsu

× Narita, Akimitsu

en Narita, Akimitsu

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Bibliographic Information en : Angewandte Chemie International Edition

Volume Number 62, Issue Number 14, p. e20221835, Issue Date 2023-02-20
Abstract
Description Type Abstract
Description We report the synthesis of a hexabenzoperihexacene (HBPH) with two incorporated octacene substructures, which was unambiguously characterized by single-crystal X-ray analysis. The theoretical isomerization barrier of the (P,P)-/(P,M)-forms was estimated to be 38.4 kcal mol−1, and resolution was achieved by chiral HPLC. Notably, the enantiomers exhibited opposite circular dichroism responses up to the near-infrared (NIR) region (830 nm) with a high gabs value of 0.017 at 616 nm. Moreover, HBPH demonstrated NIR emission with a maximum at 798 nm and an absolute PLQY of 41 %. The excited-state photophysical properties of HBPH were investigated by ultrafast transient absorption spectroscopy, revealing an intriguing feature that was attributed to the rotational and/or conformational dynamics of HBPH after excitation. These results provide new insight into the design of chiral nanographene with NIR optical properties for potential chiroptical applications.
Language en
Publisher
Publisher Wiley-VCH GmbH
ISSN
Source Identifier Type PISSN
Source Identifier 1433-7851
ISSN
Source Identifier Type EISSN
Source Identifier 1521-3773
PubMedNo.
Relation Type isIdenticalTo
Identifier Type PMID
Related Identifier 36727244
DOI
Relation Type isIdenticalTo
Identifier Type DOI
Related Identifier 10.1002/anie.202218350
Rights
Rights © 2023 The Authors.
Rights
Rights Resource https://creativecommons.org/licenses/by/4.0/
Rights Creative Commons Attribution 4.0 International
Related site
Relation Type isIdenticalTo
Identifier Type URI
Related Identifier https://onlinelibrary.wiley.com/doi/10.1002/anie.202218350
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Version Type VoR
Version Type Resource http://purl.org/coar/version/c_970fb48d4fbd8a85
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