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Bildstein, B., Denifl, P., Wurst, K., André, M., Baumgarten, M., Friedrich, J. and Ellmerer-Müller, E. (1995) Tetraferrocenylethylene, a Chiral, Organometallic Propeller: Synthesis, Structure, and Electrochemistry. Organometallics, 14, 4334-4342.
https://doi.org/10.1021/om00009a042

has been cited by the following article:

• TITLE: Synthesis and Spectroscopic Properties of Ferrocenyl Derivative Containing Donor and Acceptor Groups

  AUTHORS: Makoto Minato, Chiharu Sorai, Takashi Ito, Masashi Kiguchi, Midori Kato

  KEYWORDS: Nonlinear Optical Material, Ferrocenyl Derivative, Solvatochromic Property, SHG Efficiency

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.7 No.3, September 7, 2017

  ABSTRACT: Much interest has been devoted to organometallic NLO materials. We have become interested in exploring the utility of ferrocenyl group as the conjugating bridge. Thus, we synthesized 1-{{[1,3-(5-methylbenzo)dithiol]-2-yli- dene}methyl}-1’-[2-(p-nitrophenyl)-(E)-ethenyl]ferrocene (1). This new ferrocenyl compound has a donor and an acceptor group in 1,1’-positions. Investigations of the solvatochromic property of the compound revealed that it has polarized structure in a polar solvent, such as DMF. SHG efficiency of the compound was estimated by an SHEW (second-harmonic generation with the evanescent wave) method.