The Dihydroindeno[2,1‐<i>c</i>]fluorene Core: From Syntheses to Properties and Potential Applications

In the last decade, substances possessing the dihydroindeno[2,1‐ c ]fluorene scaffold show interesting photophysical properties and other potential applications in electronics. The aforementioned compounds belong to the family of five regioisomeric dihydroindenofluorenes, but unlike other ones, they possess angular or, in the case of higher congeners, helical shape. This review is mainly focused on various synthetic approaches to compounds possessing the dihydroindeno[2,1‐ c ]fluorene scaffold and their conversions to other polyaromatic hydrocarbons. In addition, their physicochemical and photophysical properties, and current and/or potential applications are briefly described as well.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-05-07
DOI
https://doi.org/10.1002/ejoc.202500036
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

The Dihydroindeno[2,1‐c]fluorene Core: From Syntheses to Properties and Potential Applications

Timothée Cadart, Martin Kotora
European Journal of Organic Chemistry
Organic Chemistry Cycloaddition Reactions
article

The Dihydroindeno[2,1‐c]fluorene Core: From Syntheses to Properties and Potential Applications

Timothée Cadart, Martin Kotora
article en

Abstract

In the last decade, substances possessing the dihydroindeno[2,1‐ c ]fluorene scaffold show interesting photophysical properties and other potential applications in electronics. The aforementioned compounds belong to the family of five regioisomeric dihydroindenofluorenes, but unlike other ones, they possess angular or, in the case of higher congeners, helical shape. This review is mainly focused on various synthetic approaches to compounds possessing the dihydroindeno[2,1‐ c ]fluorene scaffold and their conversions to other polyaromatic hydrocarbons. In addition, their physicochemical and photophysical properties, and current and/or potential applications are briefly described as well.

European Journal of Organic ChemistryVol. 28(32)
Charles University (CZ)
Univerzita Karlova v Praze, Grantová Agentura České Republiky
Openalex Percentile: Top 93%
Organic Chemistry Cycloaddition Reactions
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