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 language | English |
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Pages (from-to) | 457-461 |
Number of pages | 5 |
Journal | Dyes and Pigments |
Volume | 77 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2008 |
Funding
This work was supported by the Research Fund of the Technical University of Istanbul and TUBITAK-TBAG.
Funders | Funder number |
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TUBITAK-TBAG | |
Istanbul Teknik Üniversitesi |
Keywords
- Hexylthio
- Metallophthalocyanines
- Regioselective nucleophilic aromatic substituents