Tunable electronic coupling in iron–chromium mixed-valence ions of methylated Cp-indene ligands

A series of heterobimetallic η6-[(ferrocenyl)indene]-Cr(CO)3 complexes differing for the position of the ferrocenyl group, 1-(ferrocenyl)indene and 2-(ferrocenyl)indene, and the degree of indene methylation (tetramethyl- and hexamethyl-) have been prepared and studied with the aim to stabilise the mono- and dications generated by chemical and electrochemical oxidation, and at same time to tune the metal–metal electronic coupling in the mixed-valence cations. The magnitude of electronic delocalisation and spin density in the cations have been monitored by means of optical techniques (UV–Vis, near-IR, mid-IR) and EPR spectroscopy. The results have been rationalised in the framework of Marcus-Hush theory and at quantum chemistry level by DFT and TD-DFT methods, establishing that a metal-to-metal electronic coupling occurs the magnitude of which depends on the degree of indene methylation.

Mixed-valence ions of a series of differently substituted (ferrocenyl)indenes cromotricarbonyl complexes display near-IR absorption bands, the energy and intensity of which increase with the degree of methylation. Metal-to-metal electronic coupling occurs and the rate of the electron transfer raises with methylation.Figure optionsDownload as PowerPoint slide