Synthesis, structures and electrochemical properties of Group 6 metal carbonyl complexes containing ferrocenylpyrazole ligands

Abstract

A series of carbonylchromium, molybdenum and tungsten complexes containing ferrocenylpyrazole ligands, (M(CO) 5L) (M=Cr, Mo or W; L represents ferrocenyl pyrazole), have been prepared by the photochemical reactions of ferrocenylpyrazole ligands with M(CO) 6. Their electrochemical behaviors have also been investigated by cyclic voltammetry, indicating that chromium complexes exhibit two one-electron reversible or quasi-reversible couples, while molybdenum and tungsten complexes have one reversible couple corresponding to the ferrocenyl group and one irreversible oxidation process for the molybdenum or tungsten center. The crystal structures of 3-ferrocenylpyrazole pentacarbonyltungsten ( 3) and 3-methyl-5-ferrocenylpyrazole pentacarbonyltungsten ( 6) are determined by X-ray diffraction method, indicating that both 3(5)-ferrocenylpyrazole and 3(5)-methyl-5(3)-ferrocenylpyrazole act as a monodentate ligand, and the central metal of W is six-coordinate with a quasi-octahedral coordination geometry in both complexes. Complex 3 is linked into a one-dimensional chain in solid through intermolecular hydrogen bonds formed by metal carbonyl as hydrogen bond acceptors, while complex 6 forms a dimer by similar intermolecular hydrogen bond interactions. The N–H⋯O distances in complexes 3 and 6 are 2.932(11) and 2.900 Å, respectively. All new compounds have been characterized by elemental analyses, IR, 1H-NMR. 13C-NMR spectra of molybdenum and tungsten complexes have also been determined.