Pentamethylcyclopentadienyl organoiron(II) hydrazone complexes: Synthesis, spectroscopic characterization, and second-order nonlinear optical properties. X-ray crystal structure of image

A series of novel pentamethylated sandwich complexes based on the [Cp∗Fe(η6-C6H5)]+ core (Cp∗ = η5-C5Me5) has been prepared. The new organometallic π-conjugated push–pull chromophores View the MathML source[Cp∗Fe(η6-C6H5)-NHNCHR]+PF6- (R = 2,4,6-Me3C6H2, 4; (η5-C5H5)Fe(η5-C5H4), 5) were prepared through condensations between the organometallic hydrazine precursor View the MathML source[Cp∗Fe(η6-C6H5NHNH2)]+PF6- (3), and either the mesitaldehyde or the ferrocenecarboxaldehyde, respectively. Their original design combines the cationic mixed sandwich acceptor (A) associated with an organic or organometallic donor (D) through the asymmetric hydrazone spacer –NH–Ndouble bond; length as m-dashCH–. The mesityl ring of 4 has been complexed by the arenophile Cp∗Ru+, leading to the first η6:η6-coordinated dinucleating hydrazone complex, View the MathML source[Cp∗Fe(η6-C6H5)-NHNCH-{(η6-2,4,6-Me3C6H2)RuCp∗}]2+[PF6-]2 (6). Both the mono- and dinuclear hydrazones were stereoselectively obtained as their trans-isomers about the Ndouble bond; length as m-dashC double bond. All the new compounds were thoroughly characterized by a combination of elemental analysis and spectroscopic techniques (1H and 13C NMR, IR and UV–Vis). In addition, the solid-state structure of the organometallic hydrazine precursor 3 has been determined by X-ray diffraction study. Spectroscopic and electrochemical data of the organometallic hydrazones 4 and 5 clearly indicate a mutual donor–acceptor electronic influence resulting from conjugation between the end groups through the entire hydrazone backbone. Compounds 4 and 5 are strongly polarized D–π–A systems exhibiting low-lying intramolecular charge transfer bands in their electronic absorption spectra and enhanced second-order NLO properties (μβ), as measured by EFISH technique at 1.907 μm.