Redox-responsive organometallic foldamers from ferrocene amino acid: solid-phase synthesis, secondary structure and mixed-valence properties

Dalton Trans. 2011 Apr 14;40(14):3558-75. doi: 10.1039/c0dt01528h. Epub 2011 Mar 3.

Abstract

Oligoferrocenes Fmoc-Fca(n)-OMe (n=3-5) are assembled in a stepwise precise manner from Fmoc-protected ferrocene amino acid Fmoc-Fca-OH (H-Fca-OH = 1-amino-1'-ferrocene carboxylic acid; Fmoc = 9-fluorenylmethyloxycarbonyl) via amide bonds on solid supports by sequential Fmoc deprotection, acid activation and coupling steps. The resulting well-defined oligomers form ordered zigzag structures in THF solution with characteristic hydrogen bonding patterns. Electrochemical experiments reveal sequential oxidations of the individual ferrocene units in these peptides giving mixed-valent cations. Optical intervalence electron transfer is detected by intervalence transitions in the near-IR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry*
  • Dipeptides / chemistry
  • Ferrous Compounds / chemistry*
  • Fluorenes / chemistry
  • Metallocenes
  • Models, Molecular
  • Organometallic Compounds / chemistry*
  • Oxidation-Reduction
  • Peptidomimetics / chemical synthesis*
  • Peptidomimetics / chemistry*
  • Protein Structure, Secondary
  • Solutions
  • Spectrum Analysis

Substances

  • 9-fluorenylmethoxycarbonyl
  • Amino Acids
  • Dipeptides
  • Ferrous Compounds
  • Fluorenes
  • Metallocenes
  • Organometallic Compounds
  • Peptidomimetics
  • Solutions
  • ferrocene