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Tunable electronic coupling in ironchromium mixed-valence ions (Articolo in rivista)

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Tunable electronic coupling in ironchromium mixed-valence ions (Articolo in rivista) (literal)

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Santi S. 1,Orian L. 1, Donoli A. 1, Durante C. 1, Bisello A. 1, Di Valentin M. 1, Ganis P.1, Benetollo F. 2, Ceccon A. 1 (2008)
Tunable electronic coupling in ironchromium mixed-valence ions
in Journal of organometallic chemistry (Print)
(literal)

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Santi S. 1,Orian L. 1, Donoli A. 1, Durante C. 1, Bisello A. 1, Di Valentin M. 1, Ganis P.1, Benetollo F. 2, Ceccon A. 1 (literal)

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1. Dipartimento di Scienze Chimiche, Università degli Studi di Padova. 2. CNR, Istituto di Chimica Inorganica e delle Superfici, Padova. (literal)

Titolo

Abstract

A series of heterobimetallic n6-((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 monoand dications generated by chemical and electrochemical oxidation, and at same time to tune the metalmetal 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 (UVVis, 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. (literal)

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