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Theoretical study of the water oxidation mechanism with non-heme Fe (Pytacn) iron complexes. Evidence that the FeIV(O)(Pytacn) species cannot react with the water molecule to form the O-O bond

Recent studies have shown that non-heme iron complexes [Fe(L N4)X2], where LN4 stands for a tetradentate nitrogen based aminopyridine ligand (LN4 = Pytacn, mcp or mep, Pytacn = 1-(2-pyridylmethyl)-4,7-dimethyl-1,4,7-triazacyclononane, mcp = N,N-dimethyl-N,N-bis(2-pyridylmethyl)cyclohexane-trans-1,2-diamine, mep = N,N-dimethyl-N,N-bis(2-pyridylmethyl)ethylendiamine), and X are monodentate ligands (X = Cl, CH3CN, CF3SO3 -, or H2O), catalyze the oxidation of water using cerium(IV) ammonium nitrate (CAN) as oxidant. Spectroscopic monitoring of catalytic water oxidation with [Fe(CF3SO3)2(Pytacn)] established [Fe IV(O)(OH2)(Pytacn)]2+ as an intermediate along the catalytic pathway, raising the question if these high valent species could be directly responsible for the O-O bond formation event. Herein, this question is addressed by a computational analysis of the thermodynamic and kinetic parameters associated with the reaction of non-heme iron complexes [Fe IV(O)(OH)(Pytacn)]+, [FeIV(O)(OH 2)(Pytacn)]2+, and [FeIV(OH)(OH)(Pytacn)] 2+ with water. Two different mechanisms have been studied for [FeIV(O)(OH)(Pytacn)]+; the nucleophilic water attack assisted by the hydroxyl group as internal base, which is the lowest energy path, and the external nucleophilic water attack. For [FeIV(OH)(OH) (Pytacn)]2+, only the attack assisted by the internal base has been studied, while in the case of [FeIV(O)(OH2)(Pytacn)] 2+, the only viable mechanism is the external nucleophilic water attack. Up to four water molecules were needed to be included in modeling of the O-O bond formation event for a proper description of the external nucleophilic water attack. The lowest Gibbs energy barrier and reaction free energy found for the direct water nucleophilic attack to the oxo ligand are of 32.2 and 28.3 kcal·mol-1 for [FeIV(O)(OH)(Pytacn)]+, 52.0 and 40.5 kcal·mol-1 for [FeIV(O)(OH 2)(Pytacn)]2+, and 28.3 and 28.3 kcal·mol -1 for [FeIV(OH)(OH)(Pytacn)]2+, respectively. These energy barriers and endergonic reaction energies are too high for the reaction to proceed and inconsistent with the relatively rapid reaction rates determined experimentally (δG‡ (exp.) = 17.6 kcal·mol-1). Therefore, this study provides strong evidence against the O-O bond formation by these species. The energetic accessibilities of FeV(O) and FeVI(O) intermediates have also been investigated, showing that FeV is the higher oxidation state accessible under catalytic conditions, consistent with our previous results

We thank the European Research Foundation for Projects FP7-PEOPLE-2010-ERG-268445 (J.L.-F.) and ERC-2009-StG-239910 (M.C.), MICINN for projects CTQ2012-37420-C02-01/BQU (M.C.) and CTQ2011-23156/BQU (J.M.L.) and for a Ramon y Cajal contract (J.L.-F), and Generalitat de Catalunya for an ICREA Academia Award and Project 2009SGR637

© Inorganic Chemistry, 2014, vol. 53, p. 5474-5485

American Chemical Society (ACS)

Author: Acuña-Parés, Ferran
Costas Salgueiro, Miquel
Luis Luis, Josep Maria
Lloret Fillol, Julio
Date: 2014
Abstract: Recent studies have shown that non-heme iron complexes [Fe(L N4)X2], where LN4 stands for a tetradentate nitrogen based aminopyridine ligand (LN4 = Pytacn, mcp or mep, Pytacn = 1-(2-pyridylmethyl)-4,7-dimethyl-1,4,7-triazacyclononane, mcp = N,N-dimethyl-N,N-bis(2-pyridylmethyl)cyclohexane-trans-1,2-diamine, mep = N,N-dimethyl-N,N-bis(2-pyridylmethyl)ethylendiamine), and X are monodentate ligands (X = Cl, CH3CN, CF3SO3 -, or H2O), catalyze the oxidation of water using cerium(IV) ammonium nitrate (CAN) as oxidant. Spectroscopic monitoring of catalytic water oxidation with [Fe(CF3SO3)2(Pytacn)] established [Fe IV(O)(OH2)(Pytacn)]2+ as an intermediate along the catalytic pathway, raising the question if these high valent species could be directly responsible for the O-O bond formation event. Herein, this question is addressed by a computational analysis of the thermodynamic and kinetic parameters associated with the reaction of non-heme iron complexes [Fe IV(O)(OH)(Pytacn)]+, [FeIV(O)(OH 2)(Pytacn)]2+, and [FeIV(OH)(OH)(Pytacn)] 2+ with water. Two different mechanisms have been studied for [FeIV(O)(OH)(Pytacn)]+; the nucleophilic water attack assisted by the hydroxyl group as internal base, which is the lowest energy path, and the external nucleophilic water attack. For [FeIV(OH)(OH) (Pytacn)]2+, only the attack assisted by the internal base has been studied, while in the case of [FeIV(O)(OH2)(Pytacn)] 2+, the only viable mechanism is the external nucleophilic water attack. Up to four water molecules were needed to be included in modeling of the O-O bond formation event for a proper description of the external nucleophilic water attack. The lowest Gibbs energy barrier and reaction free energy found for the direct water nucleophilic attack to the oxo ligand are of 32.2 and 28.3 kcal·mol-1 for [FeIV(O)(OH)(Pytacn)]+, 52.0 and 40.5 kcal·mol-1 for [FeIV(O)(OH 2)(Pytacn)]2+, and 28.3 and 28.3 kcal·mol -1 for [FeIV(OH)(OH)(Pytacn)]2+, respectively. These energy barriers and endergonic reaction energies are too high for the reaction to proceed and inconsistent with the relatively rapid reaction rates determined experimentally (δG‡ (exp.) = 17.6 kcal·mol-1). Therefore, this study provides strong evidence against the O-O bond formation by these species. The energetic accessibilities of FeV(O) and FeVI(O) intermediates have also been investigated, showing that FeV is the higher oxidation state accessible under catalytic conditions, consistent with our previous results
We thank the European Research Foundation for Projects FP7-PEOPLE-2010-ERG-268445 (J.L.-F.) and ERC-2009-StG-239910 (M.C.), MICINN for projects CTQ2012-37420-C02-01/BQU (M.C.) and CTQ2011-23156/BQU (J.M.L.) and for a Ramon y Cajal contract (J.L.-F), and Generalitat de Catalunya for an ICREA Academia Award and Project 2009SGR637
Format: application/pdf
ISSN: 0020-1669 (versió paper)
1520-510X (versió electrònica)
Document access: http://hdl.handle.net/10256/10209
Language: eng
Publisher: American Chemical Society (ACS)
Collection: MINECO/PN 2013-2015/CTQ2012-37420-C02-01
MICINN/PN 2012-2014/CTQ2011-23156
AGAUR/2009-2014/2009 SGR-637
Reproducció digital del document publicat a: http://dx.doi.org/10.1021/ic500108g
Articles publicats (D-Q)
info:eu-repo/grantAgreement/EC/FP7/268445
info:eu-repo/grantAgreement/EC/FP7/239910
Is part of: © Inorganic Chemistry, 2014, vol. 53, p. 5474-5485
Rights: Tots els drets reservats
Subject: Ferro -- Compostos
Iron compounds
Oxidació
Oxidation
Catàlisi homogènia
Homogeneous catalysis
Title: Theoretical study of the water oxidation mechanism with non-heme Fe (Pytacn) iron complexes. Evidence that the FeIV(O)(Pytacn) species cannot react with the water molecule to form the O-O bond
Type: info:eu-repo/semantics/article
Repository: DUGiDocs

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