0000000000807624

AUTHOR

Michael Linseis

0000-0003-0861-8537

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Oligonuclear Ferrocene Amides: Mixed‐Valent Peptides and Potential Redox‐Switchable Foldamers

2010

Trinuclear ferrocene tris-amides were synthesized from an Fmoc- or Boc-protected ferrocene amino acid, and hydrogen-bonded zigzag conformations were determined by NMR spectroscopy, molecular modelling, and X-ray diffraction. In these ordered secondary structures orientation of the individual amide dipole moments approximately in the same direction results in a macrodipole moment similar to that of α-helices composed of α-amino acids. Unlike ordinary α-amino acids, the building blocks in these ferrocene amides with defined secondary structure can be sequentially oxidized to mono-, di-, and trications. Singly and doubly charged mixed-valent cations were probed experimentally by Vis/NIR, param…

Models MolecularMagnetic Resonance SpectroscopyMolecular StructureMetallocenesHydrogen bondOrganic ChemistryInorganic chemistryMolecular ConformationGeneral ChemistryNuclear magnetic resonance spectroscopyIntervalence charge transferAmidesCatalysischemistry.chemical_compoundCrystallographyFerrocenechemistryIntramolecular forceAmideMoleculeFerrous CompoundsPeptidesOxidation-ReductionProtein secondary structureChemistry – A European Journal
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