Abstract
Metal-free and Co(II)-phthalocyanines carrying eight dodecaborate substituents (96 boron atoms) on the peripheral positions were synthesized in a multistep reaction sequence. The first step of the preparation of metal-free and Co(II) target phthalocyanines was cyclotetramerization of 4-(3,5- dimethoxyphenoxy)phthalonitrile in pentanol in the presence of lithium pentanolate and Co(II) salt, respectively. After cleavage of methyl groups the reaction of (Bu4N)[B12H11O(CH 2CH2)2O] with hydroxyphenoxy substituted phthalocyanines gives the novel phthalocyanines 7, 8 with eight dodecaborate units. The new phthalocyanine compounds were characterized by NMR, FT-IR and UV-VIS spectral data. The electrochemical investigations of cobalt(II) phthalocyanine together with Zn(II) derivative having identical substituents were studied.
Original language | English |
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Pages (from-to) | 64-71 |
Number of pages | 8 |
Journal | Journal of Organometallic Chemistry |
Volume | 755 |
DOIs | |
Publication status | Published - 1 Apr 2014 |
Keywords
- BNCT
- closo-Dodecaborate
- Cobalt
- Phthalocyanine
- Synthesis
- Zinc