Cycloaromatization approach to planar and cylindrical carbon oligomers

Grant J. Palmer; Daniel M. Bowles; Chad Landis; John E. Anthony

doi:10.1016/S0008-6223(00)00054-3

Cycloaromatization approach to planar and cylindrical carbon oligomers

Grant J. Palmer, Daniel M. Bowles, Chad Landis, John E. Anthony

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Cycloaromatization chemistry has the potential to become an important paradigm for the formation of graphic oligomers. Iterative cycloaromatization is a viable method for the preparation of linearly-fused aromatic systems. As long as solubility is maintained, the cycloaromatized products are formed in good yield, and the resulting halogenated acene oligomers can be carried-on to more extended systems.

Original language	English
Pages (from-to)	1671-1674
Number of pages	4
Journal	Carbon
Volume	38
Issue number	11
DOIs	https://doi.org/10.1016/S0008-6223(00)00054-3
State	Published - 2000

Bibliographical note

Funding Information:
The authors wish to express their thanks to the Camille and Henry Dreyfus Foundation (New Faculty Award to JA), the National Science Foundation (CHE-9875123) and the Office of Naval Research for support of this work.

ASJC Scopus subject areas

Chemistry (all)
Materials Science (all)

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abstract = "Cycloaromatization chemistry has the potential to become an important paradigm for the formation of graphic oligomers. Iterative cycloaromatization is a viable method for the preparation of linearly-fused aromatic systems. As long as solubility is maintained, the cycloaromatized products are formed in good yield, and the resulting halogenated acene oligomers can be carried-on to more extended systems.",

author = "Palmer, {Grant J.} and Bowles, {Daniel M.} and Chad Landis and Anthony, {John E.}",

note = "Funding Information: The authors wish to express their thanks to the Camille and Henry Dreyfus Foundation (New Faculty Award to JA), the National Science Foundation (CHE-9875123) and the Office of Naval Research for support of this work.",

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AU - Palmer, Grant J.

AU - Bowles, Daniel M.

AU - Landis, Chad

AU - Anthony, John E.

N1 - Funding Information: The authors wish to express their thanks to the Camille and Henry Dreyfus Foundation (New Faculty Award to JA), the National Science Foundation (CHE-9875123) and the Office of Naval Research for support of this work.

PY - 2000

Y1 - 2000

N2 - Cycloaromatization chemistry has the potential to become an important paradigm for the formation of graphic oligomers. Iterative cycloaromatization is a viable method for the preparation of linearly-fused aromatic systems. As long as solubility is maintained, the cycloaromatized products are formed in good yield, and the resulting halogenated acene oligomers can be carried-on to more extended systems.

AB - Cycloaromatization chemistry has the potential to become an important paradigm for the formation of graphic oligomers. Iterative cycloaromatization is a viable method for the preparation of linearly-fused aromatic systems. As long as solubility is maintained, the cycloaromatized products are formed in good yield, and the resulting halogenated acene oligomers can be carried-on to more extended systems.

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Cycloaromatization approach to planar and cylindrical carbon oligomers

Abstract

Bibliographical note

ASJC Scopus subject areas

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