Ultrafast photoinduced processes in subphthalocyanine electron donor-acceptor conjugates linked by a single B-N bond

Org Lett. 2012 Nov 16;14(22):5656-9. doi: 10.1021/ol302632u. Epub 2012 Oct 26.

Abstract

We have prepared two different subphthalocyanine conjugates by linking these macrocycles either to an electron-accepting perylene diimide or to an electron-donating phenothiazine through a single B-N covalent bond. The short spacing between the two active building blocks results in ultrafast photoinduced electron-transfer reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Imides
  • Macrocyclic Compounds / chemistry*
  • Molecular Conformation
  • Molecular Structure
  • Perylene / analogs & derivatives
  • Phenothiazines / chemistry*
  • Photochemical Processes

Substances

  • Imides
  • Macrocyclic Compounds
  • Phenothiazines
  • perylenediimide
  • Perylene