Abstract
Two heteroleptic Ni(II) complexes combined the redox-active catecholate and 2,2'- bipyridine ligand platforms were synthesized to observe a photoinduced intramolecular ligand-to-ligand charge transfer (LL'CT, HOMO(catecholate) → LUMO(α-diimine)). A molecular design of compound [Ni(II)(3,6-Cat)(bipy)]∙CH(3)CN (1) on the base of bulky 3,6-di-tert-butyl-o-benzoquinone (3,6-DTBQ) was an annelation of the ligand with an electron donor glycol fragment, producing derivative [Ni(II)(3,6-Cat(gly))(bipy)]∙CH(2)Cl(2) (2), in order to influence the energy of LL'CT transition. A substantial longwave shift of the absorption peak was observed in the UV-Vis-NIR spectra of 2 compared with those in 1. In addition, the studied Ni(II) derivatives demonstrated a pronounced negative solvatochromism, which was established using a broad set of solvents. The molecular geometry of both compounds can be ascribed as an insignificantly distorted square-planar type, and the π-π intermolecular stacking of the neighboring α-diimines is realized in a crystal packing. There is a lamellar crystal structure for complex 1, whereas the perpendicular T-motifs with the inter-stacks attractive π-π interactions form the packing of complex 2. The redox-active nature of ligand systems was clearly shown through the electrochemical study: a quasi-reversible one-electron reduction of 2,2'-bipyridine and two reversible successive one-electron oxidative conversations ("catecholate dianion-o-benzosemiquinonato radical anion-neutral o-benzoquinone") were detected.