Three polyoxometalates (POMs) functionalized by tetrathiafulvalene (TTF) molecules have been synthesized by a coupling reaction between the Anderson-type POMs [MnMo₆O₁₈{(OCH₂)₃CNH₂}₂]^3- or [AlMo₆O₁₈(OH)₃{(OCH₂)₃CNH₂}]^3- and the TTF carboxylic acid derivative (MeS)₃TTF(S-CH₂-CO₂H). The monofunctionalized TTF-AlMo₆ POM contains one TTF group covalently grafted on an Al Anderson platform. The symmetrical TTF-MnMo₆-TTF POM possesses two TTF groups grafted on each side of a Mn Anderson derivative while the asymmetrical TTF-MnMo₆-SP POM contains a TTF and a spiropyran groups. These three trianionic species have been characterized by elemental analysis, ¹H and ¹³C NMR, FT-IR spectroscopy, ESI-MS spectrometry, and single-crystal X-ray diffraction (for TTF-MnMo₆-TTF). In the solid state, the grafted TTF molecules of TTF-MnMo₆-TTF POMs interact via S···S and π···π interactions and form chains. The electrochemical properties of the complexes reflect the contributions of both the inorganic POM and the TTF moieties. Despite adsorption of the oxidized hybrid species on the Pt grid working electrode, UV-vis-NIR spectroelectrochemical investigations evidence peaks characteristic of the oxidation of the TTF units. Finally, hyper-Rayleigh scattering (HRS) measurements show that the three novel TTF derivatives exhibit β values between 20 and 37 × 10^-30 esu. Moreover it is observed that the oxidation of the TTF moieties by Fe³⁺ ions increases the NLO response. These values are in the order of magnitude of that found for the well-known 4-dimethylamino- N-methyl-4-stilbazolium (DAS⁺) cation (β = 60 × 10^-30 esu).

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