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J Am Chem Soc. 2005 Jun 8;127(22):8028-9.

Functionalized higher acenes: hexacene and heptacene.

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  • 1Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.

Abstract

We have extended our functionalization strategy for pentacene to the higher acenes hexacene and heptacene. Provided a large enough alkyne substituent is used, these large aromatic rods are both stable and soluble and can be characterized spectroscopically as well as by single-crystal X-ray diffraction.

PMID:
15926823
[PubMed]
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