The addition of bis(2,4,6-triisopropylphenyl)tin dichloride (1) to a hexane/THF slurry of 1,1‘-dilithioferrocene−tmeda produces the corresponding stannyleneferrocenophane (2) in good yield. Structural analysis of 2 reveals a dihedral angle between the two cyclopentadienyl rings of 14.7° and a relatively short Fe−Sn atomic distance of 2.994(2) Å. Cyclic voltammetry of 2 exhibits reversible redox behavior. Whereas treatment with MeOH and H2O failed to produce ring-opened compounds, silica gel catalyzed hydrolysis of 1 leads to ring-opened Fc(i-Pr3C6H2)2SnOH (3), which crystallizes as a H-bonded dimer. Thermal treatment of 2 at 180 °C leads to the ring-opened polymerization product 4, which after precipitation from toluene remains insoluble in organic solvents. Solid-state 13C and 119Sn NMR spectra of 4 confirm the structure of the material. The X-ray structural analysis of 1 is reported and compared to that of 2.

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