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Tetranuclear Iron Complexes Bearing Benzenetetrathiolate Bridges as Four-Electron Transformation Templates and Their Electrocatalytic Properties for Proton Reduction
Vise andre og tillknytning
2013 (engelsk)Inngår i: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 52, nr 4, s. 1798-1806Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Two tetranuclear iron-sulfur complexes, (mu,mu-pbtt)[Fe-2(CO)(6)](2) (pbtt = benzene-1,2,4,5-tetrathiolato, 3) and (mu,mu-obtt)[Fe-2(CO)(6)](2) (obtt = benzene-1,2,3,4-tetrathiolato, 4), were prepared from reaction of Fe-3(CO)(12) and the corresponding tetramercaptobenzene in THF, respectively. Complexes 5 and 6, (mu,mu-pbtt)[Fe-2(CO)(5)L-1][Fe-2(CO)(5)L-2] (L-1 = CO, L-2 = PPyr(3) (Pyr = N-pyrrolyl), 5; L-1 = L-2 = PPyr(3), 6) were obtained by controlling CO displacement of 3 with PPyr(3). Molecular structures of 3-6 were determined by spectroscopic and single-crystal X-ray analyses. All-CO Fe4S4 complexes 3 and 4 each display four-electron reduction processes in consecutive chemically reversible two-electron reduction events with relatively narrow potential spans in the cyclic voltammograms. Phosphine-substituted Fe4S4 complexes 5 and 6 exhibit two consecutive two-electron reduction events, which are not fully reversible. The electrocatalytic properties of 3 and 4 for proton reduction were studied using a series of carboxylic acids of increasing strength (CH3COOH, CH2ClCOOH, CHCl2COOH, CCl3COOH, and CF3COOH). The mechanisms for electrochemical proton reduction to hydrogen catalyzed by complex 3 as a function of acid strength are discussed.

sted, utgiver, år, opplag, sider
2013. Vol. 52, nr 4, s. 1798-1806
Emneord [en]
Fe-Only Hydrogenases, Active-Site Models, X-Ray Structures, Electrochemical Properties, Organometallic Complex, Hexacarbonyl Complexes, H-2 Evolution, Diiron, Ligands, Catalysis
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-119736DOI: 10.1021/ic301647uISI: 000315255200022Scopus ID: 2-s2.0-84874023280OAI: oai:DiVA.org:kth-119736DiVA, id: diva2:612578
Forskningsfinansiär
Swedish Research CouncilKnut and Alice Wallenberg Foundation
Merknad

QC 20130322

Tilgjengelig fra: 2013-03-22 Laget: 2013-03-21 Sist oppdatert: 2017-12-06bibliografisk kontrollert

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