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Diphosphahexaarenes as Highly Fluorescent and Stable Materials
Oligoarenes are regarded as subunits of π‐extended carbon nanoforms, such as graphene and nanotubes, with exceptional technological importance. Fused arenes can thus provide fundamental insight into the nature of the electronic properties of fused polyaromatic rings and pave the way for the design o...
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Published in: | Angewandte Chemie 2018-11, Vol.130 (46), p.15377-15381 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Oligoarenes are regarded as subunits of π‐extended carbon nanoforms, such as graphene and nanotubes, with exceptional technological importance. Fused arenes can thus provide fundamental insight into the nature of the electronic properties of fused polyaromatic rings and pave the way for the design of extended graphene‐like materials. However, large π‐extended arenes often show low stability. Herein we report the straightforward preparation of linearly fused diphosphahexaarenes containing two six‐membered phosphorus heterocycles. They are highly stable towards air, water, and light over months in both solution and the solid state. Single‐crystal X‐ray crystallography confirmed the molecular structure of all derivatives. Investigations of their optoelectronic properties revealed that the diphosphahexaarenes exhibit ambipolar redox behavior and high fluorescence quantum yields. Embedding six‐membered phosphorus rings into large acenes thus opens up new opportunities for the investigation of polyaromatic systems.
Zwei P‐Ringe in einer Reihe: Die einfache Synthese linear anellierter Systeme, welche zwei sechsgliedrige Phosphorheterocyclen beinhalten, sogenannte Diphosphahexaarene, wird beschrieben (siehe Strukturen). Sie sind sehr stabil gegenüber Luft, Feuchtigkeit und Licht. Optoelektronische Studien zeigten ein ambipolares Redoxverhalten und hohe Fluoreszenz‐Quantenausbeuten von bis zu 0.85. |
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ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.201809754 |