Extending the scope of a new cyanation: design and synthesis of an anthracene derivative with an exceptionally low LUMO level and improved solubility
Author(s)
Gloecklhofer, Florian
Morawietz, Andreas J
Stoeger, Berthold
Unterlass, Miriam M
Froehlich, Johannes
Type
Journal Article
Abstract
The preparation of cyanated acenes from quinones has been improved for the conversion of electron-poor starting materials. The new procedure was used to prepare rationally designed 2,7-dinitro-9,10-dicyanoanthracene. Crystallographic, morphological, and electrochemical investigations have revealed most promising properties for applications in organic electronics.
Date Issued
2017-04-30
Date Acceptance
2017-04-10
Citation
ACS Omega, 2017, 2 (4), pp.1594-1600
ISSN
2470-1343
Publisher
American Chemical Society
Start Page
1594
End Page
1600
Journal / Book Title
ACS Omega
Volume
2
Issue
4
Copyright Statement
© 2017 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY)License, which permits unrestricted use, distribution and reproduction in any medium,provided the author and source are cited.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000401698300008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Physical Sciences
Chemistry, Multidisciplinary
Chemistry
ORGANIC SEMICONDUCTORS
CYANOARENES
PRECURSORS
QUINONES
Publication Status
Published
Date Publish Online
2017-04-24