Protonation of the previously reported porphyrin [2]catenanes in strongly acidic solutions results in electrostatic repulsion of their two components, and conformational reorientations and changes in rotation rates, which are dependent on the structural flexibility of the molecules.
M. J. Gunter and M. R. Johnston, J. Chem. Soc., Chem. Commun., 1994, 829 DOI: 10.1039/C39940000829
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...