Abstract

We report the synthesis of a key mononuclear intermediate complex based on a quinoid ligand and its further metalation to afford the corresponding hetero-bimetallic compound that revealed unique properties. An unprecedented hetero-bimetallic effect in coordination chemistry could be indeed observed and exploited to prepare, through selective ligand exchange, a tetranuclear complex (Pd-Ni-Ni-Pd) absorbing light up to the far-red region. Most importantly, we describe here to the best of our knowledge the first use of bischelating ligand for ligand exchange, and this approach can be considered as a new route for incorporating planar units to access multi-heteronuclear complexes. The origin of this specific ligand exchange as well as of the nature of the electronic excited states of the relevant structures were investigated by first-principle calculations.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call