Fiche publication
Date publication
juillet 2006
Auteurs
Membres identifiés du Cancéropôle Est :
Pr LEHN Jean-Marie
,
Dr VAN DORSSELAER Alain
Tous les auteurs :
Marquis A, Smith V, Harrowfield J, Lehn JM, Herschbach H, Sanvito R, Leize-Wagner E, Van Dorsselaer A
Lien Pubmed
Résumé
Double helicates are known to exhibit self-recognition characteristics determined by the coordination geometry of the metal involved as well as by the topicity of the ligands. Combining tridentate (terpyridine, T) or bidentate (bipyridine, B) subunits in a tritopic strand affords a set of ligands able to assemble by pairs to form double helicates, homo- or heterostranded, homo- or heterotopic, depending on the coordination properties of the metals involved. The four ligand strands, BBB, TTT, BBT, and TBT form constitutionally dynamic sets of double helicates with the metal ions Cu(I), Cu(II), and Zn(II); these helicates correspond to the correct coding of the BB, BT, and TT pairs for tetra-, penta-, and hexacoordinate Cu(I), Cu(II), and Zn(II) cations, respectively.
Référence
Chemistry. 2006 Jul 17;12(21):5632-41.
