The synthesis and characterization of functionalized polyfluorinated phthalocyanines

Mukaddes Özçeşmeci, Esin Hamuryudan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

4-(2′,3′,4′,5′,6′-Pentafluorobenzyloxy)phthalonitrile was employed with hexanethiol to prepare 4-(2′,3′,5′,6′-tetrafluoro-4′-hexylthio-benzyloxy)phthalonitrile, by the selective displacement of the para-fluorine atom using K2CO3 in DMF. The new Zn(II), Ni(II) and Co(II) phthalocyanines with four, peripheral fluoro-hexylthiobenzyloxy groups were synthesized from 4-(2′,3′,5′,6′-tetrafluoro-4′-hexylthio-benzyloxy)phthalonitrile and the corresponding divalent metal salt (Zn(CH3COO)2, NiCl2 or CoCl2). The blue-green phthalocyanines were soluble in common organic solvents. The structures of the target compounds were confirmed using elemental analysis, UV-vis, FT-IR, 1H NMR, 19F NMR and mass spectroscopic methods.

Original languageEnglish
Pages (from-to)457-461
Number of pages5
JournalDyes and Pigments
Volume77
Issue number2
DOIs
Publication statusPublished - 2008

Funding

This work was supported by the Research Fund of the Technical University of Istanbul and TUBITAK-TBAG.

FundersFunder number
TUBITAK-TBAG
Istanbul Teknik Üniversitesi

    Keywords

    • Hexylthio
    • Metallophthalocyanines
    • Regioselective nucleophilic aromatic substituents

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