Oligoethylene chains terminated by ferrocenyl end groups: Synthesis, structural properties, and two-dimensional self-assembly on surfaces

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Abstract

A series of unsaturated long-chain-bridged diferrocenes Fc-(CH 2)n-CH=CH-(CH2)n-Fc (4a-e) was synthesized by means of olefin metathesis. Subsequent catalytic hydrogenation furnished the saturated α,ω-bis-ferrrocenyl oligoethylene products Fc-(CH2)m-Fc (5). Members of both series formed highly ordered laminar structures at the highly oriented pyrolytic graphite (HOPG) solid/liquid interface or on the Ag(110) surface, which were characterized by STM. Details of the structural features of these ordered physisorbed surface assemblies of 4 and 5 were analyzed by comparison with DFT calculations on model systems and with the characteristic packing modes of these systems in the crystal. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.

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Wedeking, K., Mu, Z., Kehr, G., Sierra, J. C., Lichtenfeld, C. M., Grimme, S., … Fuchs, H. (2006). Oligoethylene chains terminated by ferrocenyl end groups: Synthesis, structural properties, and two-dimensional self-assembly on surfaces. Chemistry - A European Journal, 12(6), 1618–1628. https://doi.org/10.1002/chem.200500552

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