Attempts to crystal engineer metallosupramolecular complexes from Cu(phen) 2+ building blocks and the prototypical, rod-like, exo-bidentate ligand 4,4'-bipyridine (4,4'-bipy) by layering techniques are described. Reactions of Cu(phen) 2+ (phen = 1,10-phenanthroline) with 4,4'-bipy in the presence of NO 3 counterions yielded two distinct, discrete, dinuclear, C i symmetric, dumbbell-type complexes,[{Cu(NO 3 ) 2 (phen)} 2 (4,4'-bipy)](1) and [{Cu(NO 3 )(phen)(H 2 O)} 2 (4,4'-bipy)](NO 3 ) 2 (2), depending upon the mixture of solvents used for crystallization. In compound 1, a monoand a bidentate nitrato group coordinate to Cu 2+ , whereas in 2 the monodentate nitrato groups are replaced by aqua ligands, which introduce additional hydrogen-bond donor functionality to the molecule. The crystal structure of 1 was determined by single-crystal X-ray analysis at 296 and 110 K. Upon cooling, a disorder-order transition oc-