Cyclodehydrogenation of di- and tetra(benzimidazol-2- yl)benzenes to give model 
heteroaromatic discotic systems

Wu, W. C.; Grimsdale, Andrew C.; Müllen, Klaus

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Cyclodehydrogenation of di- and tetra(benzimidazol-2- yl)benzenes to give model heteroaromatic discotic systems

Wu, W. C., Grimsdale, A. C., & Müllen, K. (2003). Cyclodehydrogenation of di- and tetra(benzimidazol-2- yl)benzenes to give model heteroaromatic discotic systems. Chemical Communications, (9), 1044-1045.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-62D0-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-62D2-F

Genre: Journal Article

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Creators:
Wu, W. C.¹, Author
Grimsdale, Andrew C.¹, Author
Müllen, Klaus¹, Author

Affiliations:
1MPI for Polymer Research, Max Planck Society, ou_1309545

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Abstract: Di- and tetra(benzimidazol-2-yl)benzenes upon oxidation undergo cyclodehydrogenation with formation of N-N bonds to form planarized polycyclic compounds which are models for the cores of heteroatom-containing discotic materials, and which can be readily reduced back to the original compounds, thus demonstrating a molecular redox switch.

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Language(s): eng - English

Dates: Date issued: 2003

Publication Status: Issued

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Identifiers: eDoc: 28359
ISI: 000182316200008
Other: P-03-30

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Title: Chemical Communications

Alternative Title : Chem. Commun.

Source Genre: Journal

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Pages: - Volume / Issue: (9) Sequence Number: - Start / End Page: 1044 - 1045 Identifier: ISSN: 1359-7345