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  Phenothiazine–Bipyridinium Oligooxacyclophanes

Petry, C., Lang, M., Staab, H. A., & Bauer, H. (1993). Phenothiazine–Bipyridinium Oligooxacyclophanes. Angewandte Chemie International Edition in English, 32(12), 1711-1714. doi:10.1002/anie.199317111.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0019-A9F3-2 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-24C5-D
Genre: Journal Article

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AngewChemIntEd_32_1993_1711.pdf (Any fulltext), 405KB
 
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http://onlinelibrary.wiley.com/doi/10.1002/anie.199317111/epdf (Any fulltext)
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https://dx.doi.org/10.1002/anie.199317111 (Any fulltext)
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 Creators:
Petry, Christoph1, Author           
Lang, Martina2, Author           
Staab, Heinz A.3, Author           
Bauer, Helmut3, Author           
Affiliations:
1Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              
2Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497704              
3Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society, ou_1497706              

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 Abstract: Surprisingly [11.11]cyclophane 1 (n = 3) shows transannular nuclear Overhauser effects (NOES) in dichloromethane and acetonitrile between the protons of the bipyridinium and those of the phenothiazine unit, indicating an attractive donor-acceptor interaction. In the [20.20]cyclophane 1 (n = 6) complexation with barium ions facilitates the approach of the donor and acceptor units.

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Language(s): eng - English
 Dates: 1993-05-081993-08-211993-12
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: eDoc: 665115
DOI: 10.1002/anie.199317111
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Title: Angewandte Chemie International Edition in English
  Other : Angew. Chem., Int. Ed. Engl.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 32 (12) Sequence Number: - Start / End Page: 1711 - 1714 Identifier: ISSN: 0570-0833
CoNE: https://pure.mpg.de/cone/journals/resource/0570-0833