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The right way to self-fuse bi- and terpyrenyls to afford graphenic cutouts.

Authors
Type
Published Article
Journal
Chemical Communications
1364-548X
Publisher
The Royal Society of Chemistry
Publication Date
Volume
49
Issue
90
Pages
10578–10580
Identifiers
DOI: 10.1039/c3cc45235b
PMID: 24091494
Source
Medline

Abstract

In this work, we subject bi- and terpyrenyls to selective fusion for formation of extended polycyclic aromatic hydrocarbons (PAHs). Connecting the pyrene units at 4-4'- or 1-4'-positions led to smooth formation of extended PAHs, achieved via cyclodehydrogenation. This is far more difficult if pyrene is coupled in the 1,1'-position.

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