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박영석

Park, Young S.
Advanced Organic Materials Lab.
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Synthesis of Polybenzoquinolines as Precursors for Nitrogen-Doped Graphene Nanoribbons

Author(s)
Dibble, David J.Park, Young S.Mazaheripour, AmirUmerani, Mehran J.Ziller, Joseph W.Gorodetsky, Alon A.
Issued Date
2015-05
DOI
10.1002/anie.201411740
URI
https://scholarworks.unist.ac.kr/handle/201301/20043
Fulltext
http://onlinelibrary.wiley.com/doi/10.1002/anie.201411740/abstract
Citation
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.54, no.20, pp.5883 - 5887
Abstract
Graphene nanoribbons (GNRs) represent promising materials for the next generation of nanoscale electronics. However, despite substantial progress towards the bottom-up synthesis of chemically and structurally well-defined all-carbon GNRs, strategies for the preparation of their nitrogen-doped analogs remain at a nascent stage. This scarce literature precedent is surprising given the established use of substitutional doping for tuning the properties of electronic materials. Herein, we report the synthesis of a previously unknown class of polybenzoquinoline-based materials, which have potential as GNR precursors. Our scalable and facile approach employs few synthetic steps, inexpensive commercial starting materials, and straightforward reaction conditions. Moreover, due to the importance of quinoline derivatives for a variety of applications, the reported findings may hold implications across a diverse range of chemical and physical disciplines
Publisher
WILEY-V C H VERLAG GMBH
ISSN
1433-7851
Keyword (Author)
graphene nanoribbonsnanotechnologyorganic electronicspolymersquinolines
Keyword
DIELS-ALDER REACTIONQUINOLINE DERIVATIVESRECENT PROGRESSPOLYQUINOLINESELECTROLUMINESCENCEHETEROJUNCTIONSHETEROCYCLESPOLYMERSHEETS

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