Exploring the acid-catalyzed substitution mechanism of [Fe4S4Cl4]2−
Author:
Affiliation:
1. School of Chemistry
2. Newcastle University
3. Newcastle upon Tyne
4. UK
5. Department of Chemistry
Abstract
Kinetic studies focussing on either the protonation or substitution step of the acid catalyzed substitution reactions of [Fe4S4Cl4]2− support a mechanism involving concomitant cluster protonation and Fe–(μ3-SH) bond cleavage.
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/DT/C5DT04008F
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2. Aconitase as Iron−Sulfur Protein, Enzyme, and Iron-Regulatory Protein
3. Mechanism of Molybdenum Nitrogenase
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2. X-ray crystal structures of [NHR3]2[Fe4S4X4] (X = PhS, R = Et or n Bu; X = Cl, R = n Bu): implications for sites of protonation in Fe–S clusters;Transition Metal Chemistry;2016-04-21
3. Binding small molecules and ions to [Fe4S4Cl4]2− modulates rate of protonation of the cluster;Dalton Transactions;2016
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