Fusing pyrene and ferrocene into a chiral, redox-active triangle
Chemical Communications, vol. 57, pp. 6660–6663
Abstract
A macrocycle that integrates three ferrocene-pyrene dyads in a triangular C2-symmetric arrangement is synthesised as a racemate in a simple one-pot approach. Crystal structural analysis reveals two enantiomeric conformers that pack alternatingly via π-π stacking and interconvert dynamically in solution. Electrochemical investigations indicate weak electrostatic interactions between Fc groups upon oxidation to a mixed valence triangle.
Authors 6
-
Affiliation as printed
Aachen 52074
Germany
Institute of Inorganic Chemistry
RWTH Aachen University
Institute of Inorganic Chemistry, RWTH Aachen University, Aachen 52074, Germany
-
Affiliation as printed
Forschungszentrum Jülich GmbH
Germany
Jülich 52425
Peter Grünberg Institute (PGI-6)
-
Affiliation as printed
Aachen 52074
Germany
Institute of Inorganic Chemistry
Peter Grünberg Institute (PGI-6)
RWTH Aachen University
Institute of Inorganic Chemistry, RWTH Aachen University, Aachen 52074, Germany
-
Affiliation as printed
Forschungszentrum Jülich GmbH
Germany
Institute of Biological Information Processing (IBI-7)
Jülich 52425
-
Affiliation as printed
Forschungszentrum Jülich GmbH
Germany
Jülich 52425
Peter Grünberg Institute (PGI-6)
-
Affiliation as printed
Aachen 52074
Germany
Institute of Inorganic Chemistry
Peter Grünberg Institute (PGI-6)
RWTH Aachen University
Institute of Inorganic Chemistry, RWTH Aachen University, Aachen 52074, Germany
Cited by 7 stored of 7
7 results
No patents citing this paper on Lens.org (checked 2026-10-06).