Ion‐Pairing Assemblies of Polarized Charged Porphyrin

The ion pairs, consisting of the polarized porphyrin Au^III complex as a dipolar π-electronic cation, formed crystal-state ion-pairing assemblies based on antiparallel stacking structures stabilized by dispersion forces along with reduced electrostatic repulsion originating from the dipole–dipole interactions.

Abstract

A porphyrin Au^III complex comprising 5,10-penatafluorophenyl units was synthesized as a dipolar π-electronic cation. The π-electronic cation was combined with anions, including a bulky borate anion and planar π-electronic anions. The dipolar π-electronic cation formed crystal-state ion-pairing assemblies based on antiparallel stacking structures, which were stabilized by interionic dipole–dipole interactions.

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