An efficient PIFA-mediated synthesis of fused diporphyrin and triply-singly interlacedly linked porphyrin array

Org Lett. 2009 Nov 19;11(22):5266-9. doi: 10.1021/ol902198w.

Abstract

An efficient and metal-free oxidative method was reported for synthesis of triply linked diporphyrins with 2.5 equiv of phenyliodine bis(trifluoroacetate) (PIFA). This reaction showed high selectivity for Zn(II) porphyrins and had been successfully applied in the synthesis of a novel triply-singly interlacedly linked porphyrin array with lower energy gap.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fluoroacetates*
  • Iodobenzenes
  • Molecular Structure
  • Organometallic Compounds / chemical synthesis*
  • Organometallic Compounds / chemistry
  • Oxidation-Reduction
  • Porphyrins / chemistry*
  • Stereoisomerism
  • Trifluoroacetic Acid / chemistry
  • Zinc / chemistry

Substances

  • Fluoroacetates
  • Iodobenzenes
  • Organometallic Compounds
  • Porphyrins
  • phenyliodine(III) bis(trifluoroacetate)
  • Trifluoroacetic Acid
  • Zinc