Pentanuclear and heptanuclear helicates by self-assembly of d10 metal ions and a rigid aromatic bis-bidentate chelator.

ABSTRACT

The self-assembly of Zn(II) and Cd(II) ions with a bis-bidentate ligand 3,5-bis(benzimidazol-2-yl)pyrazole (H 3L) was studied by Electrospray ionization mass spectrometry, (1)H NMR measurements, and single-crystal X-ray diffraction analyses. Reaction of Zn(ClO 4) 2.6H 2O and Cd(ClO 4) 2.6H 2O with H 3L in DMF gave two pentanuclear complexes [(Zn 5(mu 3-O)(H 2L) 6)(ClO 4) 2.DMF.9.5H 2O ( 1) and [Cd 5(mu 3-O)(H 2L) 6](ClO 4)(OH).4.75DMF.0.25EtOH.10.5H 2O ( 2), in which the trigonal-bipyramidal core structures are bridged by mu 3-oxo and pyrazolate rings of the monodeprotonated H 2L. When Na 3PO 4.12H 2O was used in the reaction system of CdBr 2.4H 2O and H 3L, [Cd 5(mu 3-O)(H 2L) 6]Br 2.4.5DMF.6.5H 2O ( 3) and [Cd 7(mu 6-PO 4)(mu-Br) 3(H 2L) 6](HPO 4).DMF.10H 2O ( 4) were isolated. 3 displays the same core structure as that of 2, whereas 4 exhibits a turbinate, heptanuclear core which is bridged by a mu 6-PO 4, three mu-Br, and three pyrazolate rings. All of the pentanuclear and heptanuclear cores are surrounded by three pairs of bis-bidentate H 2L (-) ligands with offset pi-pi stacking, showing propeller-like molecular structures and triple-stand helicates. Electrospray ionization mass spectrometry studies and (1)H NMR measurements demonstrate that the pentanuclear complexes have different stability in the solution, depending on the metal ions and the counteranions. Furthermore, both 1 and 2 emit blue fluorescence with nanosecond luminescent lifetimes in DMF at room temperature.