ArticleChemical science2019
Doubly zwitterionic, di-reduced, highly electron-rich, air-stable naphthalenediimides: redox-switchable islands of aromatic-antiaromatic states.
Article in Chemical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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Who cites it
6 citing papers in PubMed.
- Pnictogen bonding in imide derivatives for chiral folding and self-assembly.Chemical science · 2024Article
- Diazazethrene bisimide: a strongly electron-accepting π-system synthesizedChemical science · 2023Article
- A highly contorted push-pull naphthalenediimide dimer and evidence of intramolecular singlet exciton fission.Chemical science · 2022Article
- Facile synthesis of an ambient stable pyreno[4,5-Chemical science · 2022Article
- Cationic Organophosphorus Chromophores: A Diamond in the Rough among Ionic Dyes.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021Review
- Molecular and Supramolecular Multiredox Systems.ChemistryOpen · 2020Review
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The di-reduced state of the naphthalene moiety and its congeners have long captivated chemists as it is elusive to stabilize these intrinsically reactive electron-rich π-systems and for their emergent multifaceted properties. Herein we report the synthesis and isolation of two-electron (2e
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