Assembly of High-Spin [Fe-3] Clusters by Ligand-Based Multielectron Reduction

Marinella Mazzanti, Rosario Scopelliti, Davide Toniolo, Ivica Zivkovic
AMER CHEMICAL SOC, 2020
Journal paper

The hexanuclear [Na12Fe6(tris-cyclo-salophen)(2)(THF)(14)], 1-THF, and the trinuclear [Na6Fe3(tris-cyclo-salophen)(py)(9)], 1-py, Fe(II) clusters can be easily assembled in one step from the ligand-based reduction of the [FeII(salophen)(THF)] complex. These complexes consist of triangular cores where three Fe(II) ions are held together, within range of bonding interaction, by the hexa-amide, hexaphenolate macrocyclic ligand tris-cyclo-salophen(12-). The tris-cyclo-salophen(12-) ligand is perfectly suited for binding three Fe(II) centers at short distances, allowing for strong magnetic coupling between the Fe(II) centers. The macrocyclic ligand is generated by the reductive coupling of the imino groups of three salophen ligands, resulting in three new C-C bonds. The six electrons stored in the ligand become available for the reduction of carbon dioxide with selective formation of carbonate.

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Marinella Mazzanti, Rosario Scopelliti, Davide Toniolo, Ivica Zivkovic
AMER CHEMICAL SOC, 2020
Journal paper

Abstract

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https://infoscience.epfl.ch/record/277503?ln=en

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Related concepts (10)

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Ligand

In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves for

Carbon dioxide

Carbon dioxide (chemical formula ) is a chemical compound made up of molecules that each have one carbon atom covalently double bonded to two oxygen atoms. It is found in the gas state at room tempera

Reductionism

Reductionism is any of several related philosophical ideas regarding the associations between phenomena which can be described in terms of other simpler or more fundamental phenomena.

Carbon dioxide reduction by lanthanide(iii) complexes supported by redox-active Schiff base ligands

Nadir Jori, Marinella Mazzanti, Rosario Scopelliti, Davide Toniolo

Here we have explored the ability of Schiff bases to act as electron reservoirs and to enable the multi-electron reduction of small molecules by lanthanide complexes. We report the reductive chemistry of the Ln(iii) complexes of the tripodal heptadentate Schiff base H(3)trensal (2,2 ',2 ''-tris(salicylideneimino)triethylamine), [Ln(III)(trensal)],1-Ln(Ln = Sm, Nd, Eu). We show that the reduction of the [Eu-III(trensal)] complex leads to the first example of a Eu(ii) Schiff base complex [{K(mu-THF)(THF)(2)}(2){Eu-II(trensal)}(2)],3-Eu. In contrast the one- and two-electron reduction of the [Nd-III(trensal)] and [Sm-III(trensal)] leads to the intermolecular reductive coupling of the imino groups of the trensal ligand and to the formation of one and two C-C bonds leaving the metal center in the +3 oxidation state. The resulting one- and two electron reduced complexes [{K(THF)(3)}(2)Ln(2)(bis-trensal)],2-Ln, and [{K(THF)(3)}(2){K(THF)}(2)Ln(2)(cyclo-trensal)],4-Ln(Ln = Sm, Nd) are able to effect the reductive disproportionation of carbon dioxide by transferring the electrons stored in the C-C bonds to CO(2)to selectively afford carbonate and CO. The selectivity of the reaction contrasts with the formation of multiple CO(2)reduction products previously reported for a U(iv)-trensal system.

ROYAL SOC CHEMISTRY2020

Synthesis of Electron-Rich Uranium(IV) Complexes Supported by Tridentate Schiff Base Ligands and Their Multi-Electron Redox Chemistry

Julie Renée Michelle Andrez, Marinella Mazzanti

The synthesis, structure, and reactivity of a new complex of U(IV) with the tridentate Schiff base ligand Menaphtquinolen are reported. The reduction of the bis-ligand complexes [UX2(Menaphtquinolen) 2] (X = Cl, (1-Cl); I (1-I)) with potassium metal affords the U(IV) complex of the new tetranionic hexadentate ligand μ-bis- Menaphtquinolen formed through the intramolecular reductive coupling of the imino groups of each Menaphtquinolen unit. The solid state structure of the [U(μ-bis-Menaphtquinolen)]2 dimer 2 isolated from toluene confirms the presence of a U(IV) complex of the reduced ligand. Reactivity studies with molecular oxygen and 9,10-phenanthrenequinone show that complex 2 can act as a multielectron reducing agent releasing two electrons through the cleavage of the C-C bond to restore the original imino function of the ligand. In the resulting U(IV) and U(VI) complexes [U(9,10-phenanthrenediol)(Menaphtquinolen)2], 3, and [UO2(Menaphtquinolen)2], 4, the restored tridentate Schiff base allows for the coordination of the reduced substrate to the metal. Electrochemical studies of complex 2 show the presence of irreversible ligand centered reduction processes and of a reversible U(IV)/U(III) couple. © 2013 American Chemical Society.

2013

Ligand and Metal Based Multielectron Redox Chemistry of Cobalt Supported by Tetradentate Schiff Bases

Julie Renée Michelle Andrez, Marinella Mazzanti, Rosario Scopelliti

We have investigated the influence of bound cations on the reduction of cobalt complexes of redox active ligands and explored the reactivity of reduced species with CO2. The one electron reduction of [CoII(Rsalophen)] with alkali metals (M = Li, Na, K) leads to either ligand-centered or metal-centered reduction depending on the alkali ion. It affords either the [CoI(Rsalophen)K] complexes or the [CoII2(bis-salophen)M2] (M = Li, Na) dimers that are present in solution in equilibrium with the respective [CoI(salophen)M] complexes. The two electron reduction of [CoII(OMesalophen)] results in both ligand centered and metal centered reduction affording the Co(I)–Co(II)–Co(I) [Co3(tris-OMesalophen)Na6(THF)6], 6 complex supported by a bridging deca-anionic tris-OMesalophen10– ligand where three OMesalophen units are connected by two C–C bonds. Removal of the Na ion from 6 leads to a redistribution of the electrons affording the complex [(Co(OMesalophen))2Na][Na(cryptand)]3, 7. The EPR spectrum of 7 suggests the presence of a Co(I) bound to a radical anionic ligand. Dissolution of 7 in pyridine leads to the isolation of [CoI2(bis-OMesalophen)Na2Py4][Na(cryptand)]2, 8. Complex 6 reacts with ambient CO2 leading to multiple CO2 reduction products. The product of CO2 addition to the OMesalophen ligand, [Co(OMesalophen-CO2)Na]2[Na(cryptand)]2, 9, was isolated but CO32– formation in 53% yield was also detected. Thus, the electrons stored in the reversible C–C bonds may be used for the transformation of carbon dioxide.

2017