Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers
The Journal of Organic Chemistry1999Vol. 64(6), pp. 2070–2079
Citations Over TimeTop 10% of 1999 papers
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.
Related Papers
- → Preparation and characterisation of C60(ferrocene)2(1992)169 cited
- → Stabilization of Langmuir monolayer of hydrophobic thiocholesterol molecules(2008)8 cited
- → Möissbauer Study of Fullerene (Ferrocene)2and Decamethyl-Ferrocene(1997)11 cited
- → Syntheses and Characterization of 1,1'-Bis(3-Pyridylethynyl)Ferrocene and 1,1'-Bis(4-Pyridylethynyl)Ferrocene(2001)10 cited
- Type of Ferrocenes on Sensitivities of Ultra-fine AP and Ferrocene Mixture(2011)