Complexation behaviour of chiral tetradentate polypyridines derived from α-pinene
摘要:
A series of ligands, where two pinene-bipyridine moieties are either connected directly, or through a p-xylene bridge are investigated with respect to their complexation behaviour in solution. The bridged [5,6]-CHIRAGEN[p-xyl] ligands, which are substituted in 5' or 6' positions show self-assembly reactions, which lead to similar supramolecular species as the unsubstituted bis-pinene-bipyridines ligands studied before. The directly connected [5,6]-CHIRAGEN[0] derivatives, which are substituted at positions 5' or 6', form mononuclear complexes with helical chirality at the metal centre. (C) 2004 Published by Elsevier B.V.
Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings
作者:Mathias Düggeli、Catherine Goujon-Ginglinger、Sarah Richard Ducotterd、David Mauron、Christophe Bonte、Alexander von Zelewsky、Helen Stoeckli-Evans、Antonia Neels
DOI:10.1039/b210625f
日期:——
A series of new tetradentate ligands containing two bipyridine groups or two pyridine moieties carrying amine substituents has been synthesised either from 5'- and 6'-substituted chiral bipyridines, or from chiral pyridine derivatives. These precursors have been prepared from (-)-alpha-pinene or (-)-myrtenal, respectively. The structures of three tetradentate-, and of five chiral bipyridine ligands
Complexation behaviour of chiral tetradentate polypyridines derived from α-pinene
作者:Mathias Düggeli、Christophe Bonte、Alexander Von Zelewsky
DOI:10.1016/j.ica.2004.07.028
日期:2005.1
A series of ligands, where two pinene-bipyridine moieties are either connected directly, or through a p-xylene bridge are investigated with respect to their complexation behaviour in solution. The bridged [5,6]-CHIRAGEN[p-xyl] ligands, which are substituted in 5' or 6' positions show self-assembly reactions, which lead to similar supramolecular species as the unsubstituted bis-pinene-bipyridines ligands studied before. The directly connected [5,6]-CHIRAGEN[0] derivatives, which are substituted at positions 5' or 6', form mononuclear complexes with helical chirality at the metal centre. (C) 2004 Published by Elsevier B.V.