Issue 40, 2024

A homoleptic Fe(iv) ketimide complex with a low-lying excited state

Abstract

The reaction of 4 equiv. of Li(N[double bond, length as m-dash]C(tBu)Ph) with FeIICl2 results in isolation of [Li(Et2O)]2[FeII(N[double bond, length as m-dash]C(tBu)Ph)4] (1), in good yields. The reaction of 1 with 1 equiv. of I2 leads to formation of [FeIV(N[double bond, length as m-dash]C(tBu)Ph)4] (2), in moderate yields. 57Fe Mössbauer spectroscopy confirms the Fe(IV) oxidation state of 2, and X-ray crystallography reveals that 2 has a square planar coordination geometry along with several intramolecular H⋯C interactions. Furthermore, SQUID magnetometry indicates a small magnetic moment at room temperature, suggestive of an accessible S = 1 state. Both density functional theory and multiconfigurational calculations were done to elucidate the nature of the ground state. Consistent with the experimental results, the ground state was found to be an S = 0 state with an S = 1 excited state close in energy.

Graphical abstract: A homoleptic Fe(iv) ketimide complex with a low-lying excited state

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Article information

Article type
Edge Article
Submitted
22 Jul 2024
Accepted
04 Sep 2024
First published
10 Sep 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2024,15, 16559-16566

A homoleptic Fe(IV) ketimide complex with a low-lying excited state

P. R. Hertler, A. Sauza-de la Vega, A. Darù, A. Sarkar, R. A. Lewis, G. Wu, L. Gagliardi and T. W. Hayton, Chem. Sci., 2024, 15, 16559 DOI: 10.1039/D4SC04880F

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