Ferrocene Groups (ferrocene + groups)

Distribution by Scientific Domains


Selected Abstracts


Synthesis of Fullerene-Stoppered Rotaxanes Bearing Ferrocene Groups on the Macrocycle,

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 7 2010
Aurelio Mateo-Alonso
Abstract The synthesis, characterisation and behaviour of a series of rotaxanes containing a fulleropyrrolidine stopper and two ferrocene moieties on the macrocycle is reported. Remarkably, the presence of large and bulky ferrocene groups does not interfere either in the synthesis or in the translocation of the macrocycle induced by ,,, interactions between the macrocycle and the fullerene. The synthetic routes developed can also be applied to the preparation of rotaxane scaffolds that can be complexed to [Ru(CO)TPP] by axial coordination. Overall, the synthetic routes presented herein provide an efficient way to prepare a variety of rotaxanes and molecular shuttles with potential applications in different fields. [source]


Attachment of Amine- and Maleimide-Containing Ferrocene Derivatives onto Self-Assembled Alkanethiol and Alkanedithiol Monolayers: Voltammetric Evaluation of Cross-Linking Efficiencies and Surface Coverage of Electroactive Groups

ELECTROANALYSIS, Issue 21 2004
Yunfeng Wang
Abstract Ferrocene derivatives containing primary amines and maleimide groups were attached covalently onto N -hydrosuccinimidyl (NHS)-terminated alkanethiol self-assembled monolayers (SAMs) and SAMs of alkanedithiol. The surface coverage and efficiencies of the two cross-linking reactions were evaluated with cyclic voltammetry. All the ferrocene derivatives attached onto the alkanethiol or alkanedithiol SAMs exhibit reversible redox waves. The surface coverage of the aminated ferrocene groups was compared to that of N -hydrosuccinimidyl (NHS)-terminated alkanethiol SAM. The covalent attachment of ,-ferrocenylethylamine onto a 11,11,-dithio-bis(succinimidylundecanoate) SAM yielded an efficiency as high as 63.1%. The cross-linking efficiency of this reaction was found to increase with the nucleophilicity of the amino groups. SAMs of longer alkyl chains favor the attachment of a greater number of ferrocene derivatives. As for the Michael-type electrophilic addition between the sulfhydryl groups of the alkanedithiol SAMs and the ferrocenyl maleimide, the cross-linking efficiencies were found to range from 6.5% to 25.7%, depending on the alkanedithiol chain length. The difference in the efficiencies between the two types of cross-linking reactions might be partially attributable to the steric hindrance imposed by the SAMs and the relative sizes of the functional groups. [source]


Modulation of the Communication between Redox Centers in a Tris(ferrocene)-tren Ligand by Complexation of Lanthanide Ions

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 23 2003
Marie Heitzmann
The tripodal ligand L built on the tren platform and bearing three chemically equivalent ferrocene units was prepared and characterized. Electrochemical investigations indicate that electrostatic communication occurs between the three ferrocene groups in L, which leads to the observation of two distinct voltammetric waves. The electrochemical communication between the three ferrocene moieties is disrupted in 1:1 (L:M3+) type complexes formed between L and Y3+ or Eu3+ metal cations and their electrochemical response tends towards that of a single three-independent-electrons oxidation wave. Modulation of the electrochemical properties of L in the presence of lanthanide ions might be exploited with a view to their electrochemical sensing in organic and aqueous media. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source]


Synthesis of Fullerene-Stoppered Rotaxanes Bearing Ferrocene Groups on the Macrocycle,

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 7 2010
Aurelio Mateo-Alonso
Abstract The synthesis, characterisation and behaviour of a series of rotaxanes containing a fulleropyrrolidine stopper and two ferrocene moieties on the macrocycle is reported. Remarkably, the presence of large and bulky ferrocene groups does not interfere either in the synthesis or in the translocation of the macrocycle induced by ,,, interactions between the macrocycle and the fullerene. The synthetic routes developed can also be applied to the preparation of rotaxane scaffolds that can be complexed to [Ru(CO)TPP] by axial coordination. Overall, the synthetic routes presented herein provide an efficient way to prepare a variety of rotaxanes and molecular shuttles with potential applications in different fields. [source]