How to stabilize large soluble (hetero-)acenes

The higher acenes and azaacenes (>(aza)heptacenes) are fascinating, yet elusive materials. Their reactivity and sensitivity increases concomitantly with their size. In recent years, confinement techniques, that is isolation of acenes in matrices and on surfaces, has surpassed solution-based chemi...

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Bibliographic Details
Main Authors: Freudenberg, Jan (Author) , Bunz, Uwe H. F. (Author)
Format: Article (Journal)
Language:English
Published: 26 June 2024
In: Journal of the American Chemical Society
Year: 2024, Volume: 146, Issue: 25, Pages: 16937-16949
ISSN:1520-5126
DOI:10.1021/jacs.4c03484
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/jacs.4c03484
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Author Notes:Jan Freudenberg and Uwe H.F. Bunz
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Summary:The higher acenes and azaacenes (>(aza)heptacenes) are fascinating, yet elusive materials. Their reactivity and sensitivity increases concomitantly with their size. In recent years, confinement techniques, that is isolation of acenes in matrices and on surfaces, has surpassed solution-based chemistry with respect to accessing the larger (hetero)acenes at the price of the accessibility of no more than a couple thousands of molecules. Isolating acenes in bulk quantities and in processable form is vital for applications in organic electronics as well as from a viewpoint from basic research. In this Perspective, we will discuss after a short historical outline their degradation pathways, and then will selectively highlight recent efforts in stabilizing soluble (aza)acenes.
Item Description:Online veröffentlicht: 11. Juni 2024
Gesehen am 14.11.2024
Physical Description:Online Resource
ISSN:1520-5126
DOI:10.1021/jacs.4c03484