Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives

The one-pot synthesis of seven new (2-alkylthiobenzoyl)ferrocenes has been achieved by Friedel–Crafts acylation of ferrocene with acid chlorides generated in situ from the corresponding carboxylic acids and phosphorous trichloride. The obtained compounds were characterized by spectroscopic data (UV, IR, 1H and 13C NMR), whereas their electrochemical properties have been investigated by cyclic voltammetry. The single-crystal X-ray structure determinations for three of them are also reported. Each of the three derivatives exhibits the intramolecular C–H…O interaction which involves the donor from the cyclopentadienyl (Cp) ring and the carbonyl oxygen as acceptor. This interaction favors the coplanar arrangement of the two moieties. The angles between the vectors coinciding the C–O bonds and the corresponding Cp planes are all below 6.4°. Conventional hydrogen bonds do not exist in any of the three crystal structures but some weak intermolecular interactions of the C–H…O, C–H…S and C–H…π types have been found and analyzed in detail. Different geometrical parameters for these crystal structures as well as for 22 similar ones extracted from Cambridge Structural Database (CSD) have been compared and analyzed.

Several new (2-alkylthiobenzoyl)ferrocenes were synthesized and characterized by IR, UV and NMR spectroscopy, as well as by cyclovoltammetric measurements. Single-crystal X-ray structure determinations of three representative ketones (S-methyl, S-ethyl and S-isopropyl derivatives) are also reported.Figure optionsDownload as PowerPoint slide