Synthesis, structure and electrochemistry of ferrocene-peptide macrocycles

Dalton Trans. 2004 Jun 7:(11):1726-30. doi: 10.1039/b401039f. Epub 2004 May 5.

Abstract

Redox active cyclopeptides Fc[CSA]2 (5), Fc[Gly-CSA]2 (6), Fc[Ala-CSA]2 (7), Fc[Val-CSA](2) and Fc[Leu-CSA]2 (9) (CSA = cysteamine) which are formed by the reaction of ferrocenedicarboxylic acid with peptide cystamines at high dilutions. These systems exhibit H-bonding involving the amide NH in solution as shown by their temperature dependent NMR spectra. With the exception of 5, the ferrocene macrocycles display intramolecular N...O cross-ring H-bonding in the solid state involving the amino acids proximal to the ferrocene.

MeSH terms

  • Amides / chemistry
  • Amino Acids / chemistry
  • Crystallography, X-Ray
  • Cystamine / chemistry
  • Electrochemistry / methods
  • Ferrous Compounds / chemical synthesis
  • Ferrous Compounds / chemistry*
  • Heterocyclic Compounds / chemical synthesis
  • Heterocyclic Compounds / chemistry*
  • Magnetic Resonance Spectroscopy / methods
  • Metallocenes
  • Molecular Structure
  • Oxidation-Reduction
  • Peptides / chemical synthesis
  • Peptides / chemistry*
  • Temperature

Substances

  • Amides
  • Amino Acids
  • Ferrous Compounds
  • Heterocyclic Compounds
  • Metallocenes
  • Peptides
  • Cystamine
  • ferrocene