JOURNAL ARTICLE

Highly Efficient Benzannulation of Poly(phenylene ethynylene)s

Hasan K. ArslanJonathan D. SaathoffDavid N. BunckPaulette ClancyWilliam R. Dichtel

Year: 2012 Journal:   Angewandte Chemie International Edition Vol: 51 (48)Pages: 12051-12054   Publisher: Wiley

Abstract

Put a ring on it: Sterically congested polyarylenes can be synthesized by benzannulation reactions at each CC bond of a poly(phenylene ethynylene) (see picture), one of the most easily synthesized and versatile classes of conjugated polymers. The benzannulation reaction is highly specific and efficient, as determined by an isotopic labeling study and several complementary spectroscopic methods. Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Keywords:
Steric effects Conjugated system Phenylene Chemistry Ring (chemistry) Combinatorial chemistry Computer science Polymer Stereochemistry Organic chemistry

Metrics

60
Cited By
2.90
FWCI (Field Weighted Citation Impact)
35
Refs
0.90
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Synthesis and Properties of Aromatic Compounds
Physical Sciences →  Chemistry →  Organic Chemistry
Synthetic Organic Chemistry Methods
Physical Sciences →  Chemistry →  Organic Chemistry
Organoboron and organosilicon chemistry
Physical Sciences →  Chemistry →  Organic Chemistry
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