<div class="csl-bib-body">
<div class="csl-entry">Glöcklhofer, F., Morawietz, A. J.-A., Stöger, B., Unterlass, M. M., & Fröhlich, J. (2017). Extending the Scope of a New Cyanation: Design and Synthesis of an Anthracene Derivative with an Exceptionally Low LUMO Level and Improved Solubility. <i>ACS Omega</i>, <i>2</i>(4), 1594–1600. https://doi.org/10.1021/acsomega.7b00245</div>
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dc.identifier.issn
2470-1343
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dc.identifier.uri
http://hdl.handle.net/20.500.12708/19973
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dc.description.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.
en
dc.language.iso
en
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dc.publisher
AMER CHEMICAL SOC
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dc.relation.ispartof
ACS Omega
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dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
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dc.subject
Hydrocarbons
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dc.subject
solubility
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dc.subject
catalyst
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dc.subject
aromatic compound
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dc.subject
crystal structure
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dc.title
Extending the Scope of a New Cyanation: Design and Synthesis of an Anthracene Derivative with an Exceptionally Low LUMO Level and Improved Solubility