Synthesis and structural characterization of a single-crystal to single-crystal transformable coordination polymer.

A single-crystal to single-crystal transformable coordination polymer compound was hydrothermally synthesized. The structural rearrangement is induced by selecting a ligand that contains both strong and weaker coordinating groups. Both hydrated and dehydrated structures were determined by single crystal X-ray analysis.

Dipyridyl β-diketonate complexes and their use as metalloligands in the formation of mixed-metal coordination networks.

The iron(III) and aluminium(III) complexes of 1,3-di(4-pyridyl)propane-1,3-dionato (dppd) and 1,3-di(3-pyridyl)propane-1,3-dionato (dmppd), [Fe(dppd)(3)] 1, [Fe(dmppd)(3)] 2, [Al(dppd)(3)] 3 and [Al(dmppd)(3)] 4 have been prepared. These complexes adopt molecular structures in which the metal centres contain distorted octahedral geometries. In contrast, the copper(II) and zinc(II) complexes [Cu(dppd)(2)] 5 and [Zn(dmppd)(2)] 6 both form polymeric structures in which coordination of the pyridyl groups into the axial positions of neighbouring metal centres links discrete square-planar complexes into two-dimensional networks.

Dipyridyl beta-diketonate complexes: versatile polydentate metalloligands for metal-organic frameworks and hydrogen-bonded networks.

The Group 13 metal complexes [M(L(2))(3)], where M is Al or Ga and L(2) is 1,3-di(4-pyridyl)-1,3-propanedionato, are hexatopic metalloligands that have been used to prepare mixed-metal-organic frameworks containing interpenetrated primitive cubic networks. In contrast, the europium complex [Eu(HL(2))(3)(H(2)L(2))]Cl(4) x EtOH forms a hydrogen-bonded network following partial protonation of the pyridyl groups.