Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 9, 2005
Previous Article Next Article

Synthesis, characterization and X-ray crystal structures of cyclam derivatives. 7. Hydrogen-bond induced allosteric effects and protonation cooperativity in a macrotricyclic bisdioxocyclam receptor

Author affiliations

Abstract

The unprecedented cooperative protonation properties displayed by a barrel-shaped macrotricyclic tetraamine incorporating two 14-membered bisamide rings maintained in a face-to-face arrangement is rationalized in terms of allosteric effects upon binding of the first and third protons.

Graphical abstract: Synthesis, characterization and X-ray crystal structures of cyclam derivatives. 7. Hydrogen-bond induced allosteric effects and protonation cooperativity in a macrotricyclic bisdioxocyclam receptor

Back to tab navigation

Supplementary files

Article information


Submitted
07 Jun 2005
Accepted
29 Jun 2005
First published
19 Jul 2005

New J. Chem., 2005,29, 1121-1124
Article type
Letter

Synthesis, characterization and X-ray crystal structures of cyclam derivatives. 7. Hydrogen-bond induced allosteric effects and protonation cooperativity in a macrotricyclic bisdioxocyclam receptor

M. Meyer, L. Frémond, E. Espinosa, S. Brandès, G. Yves Vollmer and R. Guilard, New J. Chem., 2005, 29, 1121
DOI: 10.1039/B508076B

Social activity

Search articles by author

Spotlight

Advertisements