Synthesis and reactivity of [penta(4-halogenophenyl)cyclopentadienyl][hydrotris(indazolyl)borato]ruthenium(II) complexes: rotation-induced Fosbury flop in an organometallic molecular turnstile.

ABSTRACT

The preparation of ruthenium(II) complexes coordinated to a penta(4-halogeno)phenylcyclopentadienyl ligand and to the hydrotris(indazolyl)borate ligand are detailed. Our strategy involves first the coordination of the penta(4-bromo)phenylcyclopentadienyl ligand by reaction with the ruthenium-carbonyl cluster followed by the coordination of the tripodal ligand. The pentabrominated precursor was successfully converted to the pentaiodinated derivative by using the Klapars-Buchwald methodology, applied for the first time on organometallic substrates. Cross-coupling reactions were performed on both pentabromo and pentaiodo complexes to introduce in a single step the five peripheric ferrocenyl fragments required to obtain a potential molecular motor. The two ligands present in the ruthenium complexes undergo a correlated rotation that was established both experimentally by NMR experiments and an X-ray diffraction study, and theoretically by DFT calculations. The potential-energy curve obtained by DFT revealed the energy barrier of the gearing mechanism to be only 4.5 kcal mol(-1). These sterically highly constrained complexes can be regarded as organometallic molecular turnstiles.