Unconventional Kondo effect in redox active single organic macrocyclic transistors

J Am Chem Soc. 2011 Dec 7;133(48):19547-52. doi: 10.1021/ja208799q. Epub 2011 Nov 14.

Abstract

Cyclo[6]- and cyclo[8]pyrrole, two aromatic expanded porphyrins, were studied in a single-molecule transistor (SMT) setup. The analyses of these compounds allowed us to observe an uncommon absence of an even-odd effect in the Kondo resonance in discrete, metal-free organic macrocyclic compounds. The findings from the SMT measurements of these cyclopyrroles were in accord with those from cyclic voltammetry (CV) studies and theoretical analyses. These findings provide support for the notion that SMT measurements could be useful as a tool for the characterization of similar types of aromatic macrocyclic compounds.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electric Conductivity
  • Macrocyclic Compounds / chemistry*
  • Oxidation-Reduction
  • Porphyrins / chemistry*
  • Pyrroles / chemistry*
  • Transistors, Electronic*

Substances

  • Macrocyclic Compounds
  • Porphyrins
  • Pyrroles