Issue 2, 2019

Diiron(ii) pentacarbonyl complexes as CO-releasing molecules: their synthesis, characterization, CO-releasing behaviour and biocompatibility

Abstract

Four diiron(II) carbonyl complexes, [Fe2(μ-SR)3(CO)5X] (X = Br, I; R = CH2CH3, CH2CH2CH3) were facilely synthesized by reacting [Fe(CO)4X2] with monothiolates. Their potential as carbon monoxide-releasing molecules (CORMs) was systematically investigated, revealing that their CO-releasing behaviour is highly solvent-dependent. Specifically, in dimethyl sulfoxide (DMSO), the CO-releasing kinetics were fast. Intermediates with a lower oxidation state might be involved in the reaction. By contrast, in less polar solvents such as methanol, acetonitrile and dichloromethane, intermediates featuring the triiron carbonyl cation, [Fe3(μ-SCH2CH3)6(CO)6]+, were isolated. The triiron intermediate underwent further decomposition to liberate CO. One of the iodo complexes was also examined for its CO-release in PBS solution when solubilised with DMSO in the presence of deoxy-Mb and the CO-release was found to be quantitative. Furthermore, kinetic analyses were performed and the CO-release in general obeyed a first-order kinetic model. Plausible CO-releasing pathways are proposed for the parent complexes and the triiron intermediate. Assessments in cytotoxicity indicated that the cytoxicity of the diiron(II) complexes varied with both the halide and thiolate and those bearing bromide and the thiolate with longer chains were more biocompatible.

Graphical abstract: Diiron(ii) pentacarbonyl complexes as CO-releasing molecules: their synthesis, characterization, CO-releasing behaviour and biocompatibility

Supplementary files

Article information

Article type
Paper
Submitted
04 Oct 2018
Accepted
13 Nov 2018
First published
29 Nov 2018

Dalton Trans., 2019,48, 468-477

Diiron(II) pentacarbonyl complexes as CO-releasing molecules: their synthesis, characterization, CO-releasing behaviour and biocompatibility

Z. Xiao, R. Jiang, J. Jin, X. Yang, B. Xu, X. Liu, Y. He and Y. He, Dalton Trans., 2019, 48, 468 DOI: 10.1039/C8DT03982H

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