Analysis of Weak Interactions in the Crystal Packing of Inorganic Metalorganic Hybrids Based on Keggin Polyoxometalates and Dinuclear Copper(II)−Acetate Complexes

Reaction of in situ generated copper-monosubstituted Keggin polyoxometalate (POM) and copper−phenanthroline
complexes in potassium or sodium acetate buffers led to the formation of the potassium salt of
[{SiW11O39Cu(H2O)}{Cu2(phen)2(H2O)(ac)2}]4- (1) and [{Si2W22Cu2O78(H2O)}{Cu2(phen)2(H2O)(ac)2}2]8- (2, where
phen = phenanthroline and ac = acetate) hybrid polyanions, respectively. Both compounds are the first discrete
mono- and bimolecular transition-metal-substituted Keggin POMs that support a binuclear copper−acetate complex.
Despite the different nature of the POMs, the crystal packing of the two compounds is closely related, being
formed of hybrid parallel layers that give rise to an alternate sequence of inorganic and metalorganic regions. This
packing type seems to be determined by the extensive network of weak intermolecular interactions established by
the dicopper complexes, as a Hirshfeld surface analysis shows. Electron paramagnetic resonance studies indicate
that both the supported [Cu2(ac)2(phen)2(H2O)]2+ complexes and the copper(II)-monosubstituted POMs are magnetically
isolated.