posted on 2020-10-22, 22:08authored byStefan Henfling, Roman Kempt, Jennifer Klose, Agnieszka Kuc, Berthold Kersting, Harald Krautscheid
A promising
strategy for new electrically conductive coordination
polymers is the combination of d10 metal ions, which tolerate
short metal···metal distances, with dithiolene linkers,
known for their “non-innocent” redox behavior. This
study explores the coordination chemistry of 2,3-pyrazinedithiol (H2pdt) toward Cu+ and Ag+ ions, highlighting
similarities and differences. The synthetic approach, starting with
the fully protonated ligand, allowed the isolation of a homoleptic
bis(dithiolene) complex with formal CuI atoms, [Cu(H2pdt)2]Cl (1). This complex was further
transformed to a 1D coordination polymer with short metal···metal
distances, 1D[Cu(Hpdt)] (2Cu). The larger Ag+ ion directly built up a very similar
coordination polymer, 1D[Ag(Hpdt)] (2Ag), without any appearance of an intermediate
metal complex. The coordination polymer 1D[Cu(H2pdt)I] (4), like complex 1, bears fully
protonated H2pdt ligands in their dithione form. Upon heating,
both compounds underwent auto-oxidation coupled with a dehydrogenation
of the ligand to form the open-shell neutral copper(II) complex [Cu(Hpdt)2] (3) and the coordination polymer 1D[Cu2I2(H2pdt)(Hpdt)] (5), respectively. For all presented compounds, crystal structures
are discussed in-depth. Furthermore, properties of 1, 3, and those of the three 1D coordination polymers, 2Ag, 2Cu, and 4, were investigated by UV–vis–NIR
spectroscopy, cyclic voltammetry, and variable-temperature magnetic
susceptibility, and direct current (dc)-conductivity measurements.
The experimental results are compared and discussed with the aid of
DFT simulations.