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박영석

Park, Young S.
Advanced Organic Materials Lab.
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An Aza-Diels-Alder Route to Polyquinolines

Author(s)
Dibble, David J.Umerani, Mehran J.Mazaheripour, AmirPark, Young S.Ziller, Joseph W.Gorodetsky, Alon A.
Issued Date
2015-02
DOI
10.1021/ma5020726
URI
https://scholarworks.unist.ac.kr/handle/201301/20040
Fulltext
http://pubs.acs.org/doi/abs/10.1021/ma5020726
Citation
MACROMOLECULES, v.48, no.3, pp.557 - 561
Abstract
Polyquinolines have been studied since the early 1970s due to their favorable chemical, optical, electrical, and mechanical properties. However, surprisingly few synthetic strategies have been developed for the preparation of these polymers. Herein, we demonstrate the application of the aza-DielsAlder (Povarov) reaction for the synthesis of soluble polyquinolines from a bifunctional monomer. Our approach furnishes polyquinolines with a unique architecture and connectivity in only two synthetic steps from inexpensive, commercially available reagents. The reported strategy may therefore represent a welcome addition to the polymer chemists toolkit by providing ready access to a diverse library of polyquinoline-type materials
Publisher
AMER CHEMICAL SOC
ISSN
0024-9297
Keyword
LIGHT-EMITTING-DIODESELECTRON-TRANSPORT MATERIALSQUINOLINE DERIVATIVESBIOLOGICAL-ACTIVITIESCONJUGATED POLYMERSAROMATIC POLYQUINOLINESELECTROLUMINESCENCECOPOLYMERSSPECTRAPOLYANTHRAZOLINES

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