A new synthetic route to donor-acceptor porphyrins

M. John Plater, Stuart Aiken, Grant Bourhill

Research output: Contribution to journalArticle

84 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 porphyrin synthesis.

LanguageEnglish
Pages2405-2413
Number of pages9
JournalTetrahedron
Volume58
Issue number12
Early online date8 Feb 2002
DOIs
Publication statusPublished - 18 Mar 2002
Externally publishedYes

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Plater, M. John ; Aiken, Stuart ; Bourhill, Grant. / A new synthetic route to donor-acceptor porphyrins. In: Tetrahedron. 2002 ; Vol. 58, No. 12. pp. 2405-2413.
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A new synthetic route to donor-acceptor porphyrins. / Plater, M. John; Aiken, Stuart; Bourhill, Grant.

In: Tetrahedron, Vol. 58, No. 12, 18.03.2002, p. 2405-2413.

Research output: Contribution to journalArticle

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