A new synthetic route to donor -acceptor Porphyrins

Michael John Plater, S. Aiken, G. Bourhill

Research output: Contribution to journalArticle

85 Citations (Scopus)

Abstract

Some new donor-acceptor porphyrins have been prepared based on a metallated bis(ethynyl) porphyrin core. 4-(Dimethylamino)phenyl was used as the donor group and 4-nitrophenyl, 4-cyanophenyl and 5-nitrothiazoyl as the acceptor groups. Dipyrrylmethane was used for large scale porphyrin ring synthesis because the absence of methylene substituents reduces the difficulty of substituent scrambling that occurs during parphyrin synthesis. (C) 2002 Elsevier Science Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)2405-2413
Number of pages8
JournalTetrahedron
Volume58
DOIs
Publication statusPublished - 2002

Keywords

  • porphyrins and analogues
  • palladium and compounds
  • ELECTRONIC-STRUCTURE
  • CRYSTAL
  • PHTHALOCYANINE
  • POLYMER
  • SYSTEMS

Cite this

A new synthetic route to donor -acceptor Porphyrins. / Plater, Michael John; Aiken, S.; Bourhill, G.

In: Tetrahedron, Vol. 58, 2002, p. 2405-2413.

Research output: Contribution to journalArticle

Plater, Michael John ; Aiken, S. ; Bourhill, G. / A new synthetic route to donor -acceptor Porphyrins. In: Tetrahedron. 2002 ; Vol. 58. pp. 2405-2413.
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