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Quinoxalinophenanthrophenazine based cruciforms

A series of cruciform aryl-substituted quinoxalinophenanthrophenazine derivatives (QPPs) was synthesized through Suzuki-Miyaura cross-coupling of a 2,7-diborylated pyrene tetraketal building block. The QPPs were analyzed for their optoelectronic properties by absorption and emission spectroscopy, cy...

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Main Authors: Ueberricke, Lucas (Author) , Mizioch, Dennis (Author) , Ghalami, Farhad (Author) , Mildner, Felix (Author) , Rominger, Frank (Author) , Oeser, Thomas (Author) , Elstner, Marcus (Author) , Mastalerz, Michael (Author)
Format: Article (Journal)
Language:English
Published: July 27, 2021
In: European journal of organic chemistry
Year: 2021, Issue: 34, Pages: 4816-4823
ISSN:1099-0690
DOI:10.1002/ejoc.202100701
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ejoc.202100701
Verlag, kostenfrei, Volltext: https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=DOISource&SrcApp=WOS&KeyAID=10.1002%2Fejoc.202100701&DestApp=DOI&SrcAppSID=D1pZCaTrdvOlGCD31ZT&SrcJTitle=EUROPEAN+JOURNAL+OF+ORGANIC+CHEMISTRY&DestDOIRegistrantName=Wiley+%28John+Wiley+%26+Sons%29
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Author Notes:Lucas Ueberricke, Dennis Mizioch, Farhad Ghalami, Felix Mildner, Frank Rominger, Thomas Oeser, Marcus Elstner, and Michael Mastalerz
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Summary:A series of cruciform aryl-substituted quinoxalinophenanthrophenazine derivatives (QPPs) was synthesized through Suzuki-Miyaura cross-coupling of a 2,7-diborylated pyrene tetraketal building block. The QPPs were analyzed for their optoelectronic properties by absorption and emission spectroscopy, cyclic voltammetry and quantum-chemical calculations. The solid-state packing was investigated as well and evaluated for its charge transport properties by calculated charge transfer integrals.
Item Description:Gesehen am 24.09.2021
Physical Description:Online Resource
ISSN:1099-0690
DOI:10.1002/ejoc.202100701

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