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- Title
Cover Feature: Indenoannulated Tridecacyclene: An All‐Carbon Seven‐Stage Redox‐Amphoter (Chem. Eur. J. 34/2024).
- Authors
Misselwitz, Erik; Spengler, Jonas; Rominger, Frank; Kivala, Milan
- Abstract
This article, titled "Cover Feature: Indenoannulated Tridecacyclene: An All-Carbon Seven-Stage Redox-Amphoter," discusses the synthesis and properties of a nanocarbon compound with a unique structure. The compound, formed by adding indenoannulation to tridecacyclene, exhibits a saddle shape with one octagonal and multiple pentagonal rings. It is capable of undergoing seven reversible redox events, which are facilitated by the non-benzenoid moieties in charged states. The article provides more detailed information on this compound and its properties.
- Subjects
DIANIONS; ELECTRONS
- Publication
Chemistry - A European Journal, 2024, Vol 30, Issue 34, p1
- ISSN
0947-6539
- Publication type
Article
- DOI
10.1002/chem.202401746