Cyclometalation of the ligand 1,3-bis(1-alkylbenzimidazol-2-yl)benzene (1)
with palladium carboxylates leads to a trimeric complex [Pd-3(ligand)(3)(ca
rboxylate)(3)] (3). Studies in solution show that the trinuclear core is st
able but that the carboxylates are labile, undergoing intra- and intermolec
ular exchange on an NMR time scale. The structural analogue of 1, 2,6-bis(1
-alkylbenzimidazol-2-yl)pyridine (4), gives only the mononuclear species [P
d(4)(carboxylate)(2)], characterized by X-ray diffraction. This complex for
ms a trimer if one carboxylate is labilized by the addition of strong acid;
the resulting trinuclear species is readily cleaved by nucleophiles but ca
n include weakly basic anions within its cavity.