Novel phthalocyanines with pentafluorobenzyloxy-substituents

Mukaddes Selçukoǧlu, Esin Hamuryudan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

62 Citations (Scopus)

Abstract

The synthesis of pentafluorobenzyloxy substituted metal-free phthalocyanine 4 was achieved by co-cyclotetramerization of 4-(2′,3′,4′,5′,6′-pentafluorobenzyloxy)phthalonitrile (3) with hydroquinone, whereas metallophthalocyanines (MPcs) 5-7 were synthesized in the presence of zinc, cobalt or nickel salts. The compounds were characterized by their elemental analyses, UV-vis, FT-IR, 1H NMR, 19F NMR and mass spectroscopic methods.

Original languageEnglish
Pages (from-to)17-20
Number of pages4
JournalDyes and Pigments
Volume74
Issue number1
DOIs
Publication statusPublished - 2007

Funding

This work was supported by the Research Fund of the Technical University of Istanbul and State Planning Organisation (DPT).

FundersFunder number
DPT
Technical University of Istanbul and State Planning Organisation

    Keywords

    • 2,3,4,5,6-Pentafluorobenzyl alcohol
    • Copper
    • Fluorocarbons
    • Phthalocyanines
    • Zinc

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