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Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Redox behavior of rhodium 9,10-phenanthrenediimine complexes
David W Shaffer1, Scott A Ryken, Ryan A Zarkesh
1Department of Chemistry, University of California, Irvine (UCI), California 92697-2025, USA.
Abstract:
New square-planar rhodium complexes of the redox-active ligand 9,10-phenenthrenediimine (phdi) have been prepared and studied. The complexes [dpp-nacnac(CH3)]Rh(phdi) (2a; [dpp-nacnac(CH3)](-) = CH[C(Me)(N-(i)Pr(2)C(6)H(3))](2)(-)) and [dpp-nacnac(CF3)]Rh(phdi) (2b; [dpp-nacnac(CF3)](-) = CH[C(CF(3))(N-(i)Pr(2)C(6)H(3))](2)(-)) have been prepared from the corresponding [nacnac]Rh(CO)(2) synthons by treatment with Me(3)NO in the presence of the phdi ligand. Complexes 2a and 2b are diamagnetic, and their absorption spectra are dominated by intense charge-transfer transitions throughout the visible region. Electrochemical studies indicate that both the phdi ligand and the rhodium metal center are redox-active, with the [nacnac](-) ligands serving to modulate the one-electron-oxidation and -reduction redox potentials. In the case of 2a, chemical oxidation and reduction reactions provided access to the one-electron-oxidized cation, [2a](+), and one-electron-reduced anion, [2a](-), the latter of which has been characterized in the solid state by single-crystal X-ray diffraction. Solution electron paramagnetic resonance spectra of [2a](+) and [2a](-) are consistent with S = (1)/(2) spin systems, but surprisingly the low-temperature spectrum of [2a](-) shows a high degree of rhombicity, suggestive of rhodium(II) character in the reduced anion.
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