Modellverbindungen für Elektronentransfer in räumlich geordneten Systemen: Chirale und achirale Triptycenazulenchinone

Authors

  • Jörg Daub Institut für Organische Chemie Universität Regensburg Universitätsstrasse 31, Postfach, D-8400 Regensburg (Bundesrepublik Deutschland)
  • Lothar Jakob Institut für Organische Chemie Universität Regensburg Universitätsstrasse 31, Postfach, D-8400 Regensburg (Bundesrepublik Deutschland)
  • Josef Salbeck Institut für Organische Chemie Universität Regensburg Universitätsstrasse 31, Postfach, D-8400 Regensburg (Bundesrepublik Deutschland)
  • Yoshio Okamoto Chemistry Department, Faculty of Engineering Science, Osaka University Toyonaka, Osaka 560 (Japan)

DOI:

https://doi.org/10.2533/chimia.1985.393

Abstract

Stable bitriptyceneazulene quinones have been prepared by Lewis acid induced coupling of triptyceneazulene quinones. Resolution of the enantiomers succeeded by high performance liquid chromatography (HPLC) on phenylcarbamates of cellulose. Some chiroptical properties of the enantiomers are reported. Electron transfer properties have been investigated by cyclovoltammetry.

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Published

1985-12-31

Issue

Vol. 39 No. 12 (1985): Forschung/Research

Section

Articles

License

Copyright (c) 1985 Jörg Daub

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

[1]
J. Daub, L. Jakob, J. Salbeck, Y. Okamoto, Chimia 1985, 39, 393, DOI: 10.2533/chimia.1985.393.