Tetraazaarenes by the ceramidonine approach

Parantap Sarkar; Ie Rang Jeon; Fabien Durola; Harald Bock

doi:10.1039/c2nj21033a

Tetraazaarenes by the ceramidonine approach

Parantap Sarkar, Ie Rang Jeon, Fabien Durola, Harald Bock

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

7 Citations (Scopus)

Abstract

The synthesis of extended heteroarenes via the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents.

Original language	English
Pages (from-to)	570-574
Number of pages	5
Journal	New Journal of Chemistry
Volume	36
Issue number	3
DOIs	https://doi.org/10.1039/c2nj21033a
Publication status	Published - 2012 Mar

ASJC Scopus subject areas

Catalysis
Chemistry(all)
Materials Chemistry

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10.1039/c2nj21033a

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abstract = "The synthesis of extended heteroarenes via the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents.",

author = "Parantap Sarkar and Jeon, {Ie Rang} and Fabien Durola and Harald Bock",

year = "2012",

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AU - Sarkar, Parantap

AU - Jeon, Ie Rang

AU - Durola, Fabien

AU - Bock, Harald

PY - 2012/3

Y1 - 2012/3

N2 - The synthesis of extended heteroarenes via the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents.

AB - The synthesis of extended heteroarenes via the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents.

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JO - New Journal of Chemistry

JF - New Journal of Chemistry

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Tetraazaarenes by the ceramidonine approach

Abstract

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