Sorption and Magnetic Properties of Oxalato-Based Trimetallic Open Framework Stabilized by Charge-Assisted Hydrogen Bonds.

We report a new structure of {[Co(bpy)(ox)][{Cu(bpy)(ox)}Fe(ox)]}·8.5nHO presenting a rare ladder topology among oxalate-based coordination polymers with anionic chains composed of alternately arranged [Cu(bpy)(ox)] and [Fe(ox)] moieties. Along the a axis, they are separated by Co(III) units to give porous material with voids of 963.7 Å (16.9% of cell volume). The stability of this structure is assured by a network of stacking interactions and charge-assisted C-H…O hydrogen bonds formed between adjacent chains, adjacent cobalt(III) units, and alternately arranged cobalt(III) and chain motifs. The soaking experiment with acetonitrile and bromobenzene showed that water molecules (8.5 water molecules dispersed over 15 positions) are bonded tightly, despite partial occupancy. Water adsorption experiments are described by a D'arcy and Watt model being the sum of Langmuir and Dubinin-Serpinski isotherms. The amount of primary adsorption sites calculated from this model is equal 8.2 mol HO/mol, being very close to the value obtained from the XRD experiments and indicates that water was adsorbed mainly on the primary sites. The antiferromagnetic properties could be only approximately described with the simple Cu-ox-Cu dimer using = -··, thus, considering non-trivial topology of the whole Cu-Fe chain, we developed our own general approach, based on the semiclassical model (SC) and molecular field (MF) model, to describe precisely the magnetic superexchange interactions in . We established that Cu(II)-Cu(II) coupling dominates over multiple Cu(II)-Fe(III) interactions, with = -275(29) and = -3.8(1.6) cm and discussed the obtained values against the literature data.