4.1 Article

Unexpected but convenient synthesis of soluble meso-tetrakis(3,4-benzoquinone)-substituted porphyrins

Journal

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES
Volume 18, Issue 3, Pages 173-181

Publisher

WORLD SCI PUBL CO INC
DOI: 10.1142/S1088424613501071

Keywords

nitration; benzoquinone; porphyrin; lithium nitrate; oxidation

Funding

  1. World Premier International Research Center Initiative on Materials Nanoarchitectonics from MEXT, Japan
  2. Core Research for Evolutional Science and Technology (CREST) program of JST, Japan
  3. National Science Foundation [1110942]
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1110942] Funding Source: National Science Foundation
  6. Grants-in-Aid for Scientific Research [11F01760] Funding Source: KAKEN

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A new route to 3,4-benzoquinone-substituted porphyrins is reported. In attempted nitration reactions on the copper(II) or nickel(II) complexes of 5,10,15,20-tetrakis(3,5-di-t-butyl-4-hydroxyphenyl) porphyrin using lithium nitrate in acetic anhydride-acetic acid/chloroform no nitration products could be detected with the main products being the corresponding complexes of 5,10,15,20-tetrakis(3,4-dioxo-5-t-butylcyclohexa-1,5-dienyl) porphyrin. These o-quinone-substituted porphyrins are available in reasonable yield (> 50%), their synthesis is simple and they are of good solubility. The electrochemical and spectroelectrochemical properties of representative o-quinone-substituted Cu(II) and Ni(II) porphyrin derivatives are also reported.

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