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Mono- and bi-iron chalcogenocarboxylate complexes

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Abstract

A series of thiocarboxylato and selenocarboxylato monomeric CpFe(CO)2ECORCOCl and dimeric [CpFe(CO)2ECO]2R iron complexes have been synthesized and characterized. The interaction of (μ-Ex)[CpFe(CO)2]2 (E = S; x = 2–4. E = Se; x = 1) with di-acid chlorides (ClCORCOCl) in a 1:1 molar ratio gave the monomeric complexes CpFe(CO)2ECORCOCl for R = 1,3-C6H4, 2,6-C5H3N, 1,2-C6H4. However, the dimeric complexes [CpFe(CO)2ECO]2R were obtained from the same reactants in a 2:1 metal-to-ligand molar ratio in which R is 1,3-C6H4, 2,6-C5H3N or C2H4. The monomer versus dimer production mainly depends on the electronic and steric factors of the R-moiety. The new monomeric and dimeric thio- and selenocarboxylato iron complexes have been characterized by spectroscopic techniques (1H- and 13C-NMR, IR) and by elemental analysis. The structures of [CpFe(CO)2SCO]2(1,3-C6H4) and its seleno analogue [CpFe(CO)2SeCO]2(1,3-C6H4) were determined by X-ray structure determination.

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Acknowledgments

The financial support (Grant no. 93/2011) from the Deanship of Scientific Research, Jordan University of Science and Technology is gratefully acknowledged.

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Correspondence to Mohammad El-khateeb.

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El-khateeb, M., Al-Noaimi, M., Al-Rejjal, N. et al. Mono- and bi-iron chalcogenocarboxylate complexes. Transition Met Chem 38, 529–534 (2013). https://doi.org/10.1007/s11243-013-9720-x

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