Literature DB >> 30118235

NIR-Absorbing Dye Based on BF2-Bridged Azafulvene Dimer as a Strong Electron-Accepting Unit.

Hiroyuki Shimogawa1, Yasujiro Murata1, Atsushi Wakamiya1.   

Abstract

BF2-bridged azafulvene dimers designed to be strong electron-accepting units were selectively synthesized using a bulky base. Single-crystal X-ray diffraction analysis revealed that the high electron-accepting ability of this structure stems from the contribution of the π-conjugation mode of the azafulvene dimer upon formation of B-N coordination bonds. As a result of the low-lying LUMO energy of this electron-accepting unit, the corresponding D-A-D dye exhibits an intense NIR absorption band at 922 nm, which tails up to 1150 nm, while significant absorption bands in the visible region are absent. As a NIR dye this molecule exhibits moreover exceptional photostability and resistance to oxidation by atmospheric oxygen, even in dilute solution.

Entities:  

Year:  2018        PMID: 30118235     DOI: 10.1021/acs.orglett.8b02056

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Going beyond the borders: pyrrolo[3,2-b]pyrroles with deep red emission.

Authors:  Mariusz Tasior; Paweł Kowalczyk; Marta Przybył; Małgorzata Czichy; Patryk Janasik; Manon H E Bousquet; Mieczysław Łapkowski; Matt Rammo; Aleksander Rebane; Denis Jacquemin; Daniel T Gryko
Journal:  Chem Sci       Date:  2021-11-22       Impact factor: 9.825

2.  Donor-acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells.

Authors:  Tomoya Nakamura; Yasuhisa Ishikura; Noriko Arakawa; Megumi Hori; Motoi Satou; Masaru Endo; Hisashi Masui; Shinichiro Fuse; Takashi Takahashi; Yasujiro Murata; Richard Murdey; Atsushi Wakamiya
Journal:  RSC Adv       Date:  2019-03-01       Impact factor: 3.361

  2 in total

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