Intramolecular hydrogen bonding as a synthetic tool to induce chemical selectivity in acid catalyzed porphyrin synthesis

Jackson D. Megiatto, Dustin Patterson, Benjamin D. Sherman, Thomas Moore, Devens Gust, Ana Moore

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

A straightforward procedure based on the formation of intramolecular hydrogen bonds to impart selectivity in the preparation of multi-functionalized porphyrins has been developed. To illustrate the concept, the synthesis of a biomimetic artificial photosynthetic model able to undergo electron and proton transfer reactions upon irradiation is reported. This journal is

Original languageEnglish (US)
Pages (from-to)4558-4560
Number of pages3
JournalChemical Communications
Volume48
Issue number38
DOIs
StatePublished - May 14 2012

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Proton transfer
Porphyrins
Biomimetics
Hydrogen bonds
Irradiation
Acids
Electrons

ASJC Scopus subject areas

  • Metals and Alloys
  • Materials Chemistry
  • Surfaces, Coatings and Films
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Catalysis
  • Chemistry(all)

Cite this

Intramolecular hydrogen bonding as a synthetic tool to induce chemical selectivity in acid catalyzed porphyrin synthesis. / Megiatto, Jackson D.; Patterson, Dustin; Sherman, Benjamin D.; Moore, Thomas; Gust, Devens; Moore, Ana.

In: Chemical Communications, Vol. 48, No. 38, 14.05.2012, p. 4558-4560.

Research output: Contribution to journalArticle

Megiatto, Jackson D. ; Patterson, Dustin ; Sherman, Benjamin D. ; Moore, Thomas ; Gust, Devens ; Moore, Ana. / Intramolecular hydrogen bonding as a synthetic tool to induce chemical selectivity in acid catalyzed porphyrin synthesis. In: Chemical Communications. 2012 ; Vol. 48, No. 38. pp. 4558-4560.
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