Rigid π-extended triptycenes via a hexaketone precursor

A high-yielding synthesis of a rigid hexaketone is presented that can be transformed into π-extended D3h-symmetric triptycene derivatives with high internal molecular free volumes (IMFVs). The products show excellent photophysical properties combined with high specific surface areas.

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Bibliographic Details
Main Authors: Kohl, Bernd (Author) , Rominger, Frank (Author) , Mastalerz, Michael (Author)
Format: Article (Journal)
Language:English
Published: 13 January 2014
In: Organic letters
Year: 2014, Volume: 16, Issue: 3, Pages: 704-707
ISSN:1523-7052
DOI:10.1021/ol403383y
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ol403383y
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Author Notes:Bernd Kohl, Frank Rominger, and Michael Mastalerz
Description
Summary:A high-yielding synthesis of a rigid hexaketone is presented that can be transformed into π-extended D3h-symmetric triptycene derivatives with high internal molecular free volumes (IMFVs). The products show excellent photophysical properties combined with high specific surface areas.
Item Description:Gesehen am 06.10.2020
Physical Description:Online Resource
ISSN:1523-7052
DOI:10.1021/ol403383y