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Yu CJ, Chong Y, Kayyem JF, et al. Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers. J Org Chem. 1999;64(6):2070-2079doi: 10.1021/jo982392m.
Yu, C. J., Chong, Y., Kayyem, J. F., & Gozin, M. (1999). Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers. The Journal of organic chemistry, 64(6), 2070-2079. https://doi.org/10.1021/jo982392m
Yu, C. J., et al. "Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers." The Journal of organic chemistry vol. 64,6 (1999): 2070-2079. doi: https://doi.org/10.1021/jo982392m
Yu CJ, Chong Y, Kayyem JF, Gozin M. Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers. J Org Chem. 1999 Mar 19;64(6):2070-2079. doi: 10.1021/jo982392m. PMID: 11674302.
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J Org Chem. 1999 Mar 19;64(6):2070-2079. doi: 10.1021/jo982392m.

Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers.

The Journal of organic chemistry

C. J. Yu, Yoochul Chong, Jon Faiz Kayyem, Michael Gozin

Affiliations

  1. Clinical Micro Sensors Inc., 101 Waverly Drive, Pasadena, California 91105.

PMID: 11674302 DOI: 10.1021/jo982392m

Abstract

A series of phenylethynyl oligomers (I-V) possessing a ferrocene and thiol at each termini have been synthesized. These oligomers have been designed to overcome the inherent insolubility of this class of complexes by substitution at the phenyl groups with methyl and propoxy substituents. Several new reactions for preparing arenethiol-protected compounds are described. Interestingly, the generation of an arenethiol anion during base- or fluoride-catalyzed deprotection has been characterized.

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