A Polyaromatic Terdentate Binding Unit with Fused 5,6-Membered Chelates for Complexing s-, p-, d-, and f-Block Cations

Abstract

The polyaromatic terdentate ligand 6-(azaindol-1-yl)-2,2′-bipyridine (L7) combines one 5-membered chelate ring with a fused 6-membered chelate ring. It is designed to provide complexation properties intermediate between 2,2′;6′,2″-terpyridine (L1) (two fused 5-membered chelate rings) and 2,6-bis(azaindol-1-yl)pyridine (L6) (two fused 6-membered chelate rings). In polar organic solvents, L7 displays remarkable affinities for the successive fixation of two small univalent cations M = H+ or Li+, leading to stable [M(m)(L7)]m+ (m = 1–2) complexes. Upon reaction with M = Mg2+ or Zn2+ cations, the large positive charge densities borne by the metals result in the successive cooperative complexation of two ligands to give [M(L7)n]n+ (n = 1–2). For small Sc3+, unavoidable traces of water favor the formation of the protonated ligand at millimolar concentrations in acetonitrile, but the use of larger Y3+ cations leads to [Y(L7)n]n+ (n = 1, 2), for which stability constants of log(β(1,1)(Y,L7)) = 2.9(5) and log(β(1,2)(Y,L7)) = 5.3(4) are estimated. The complexation behaviors are supported by speciations in solution, thermodynamic analyses, and solution and solid-state structures.