Novel water-soluble metal-free and metallophthalocyanines: Synthesis, spectroscopic characterization and aggregation properties
In this study, the preparation of novel metal-free phthalocyanine 2, metallophthalocyanine complexes 3, 4, 5, 6 (MPcs, M = Ni, Co, Cu, Fe) with 6-oxyquinoline functional group and quaternized metallophthalocyanine derivatives 3a, 4a, 6a (MPcs, M = Ni, Co, Fe), was achieved. The reaction of 4-(quinol...
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Veröffentlicht in: | Synthetic metals 2011-03, Vol.161 (5), p.508-515 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, the preparation of novel metal-free phthalocyanine
2, metallophthalocyanine complexes
3,
4,
5,
6 (MPcs, M
=
Ni, Co, Cu, Fe) with 6-oxyquinoline functional group and quaternized metallophthalocyanine derivatives
3a,
4a,
6a (MPcs, M
=
Ni, Co, Fe), was achieved. The reaction of 4-(quinolin-6-yloxy)phthalonitrile
1 in 2-(dimethylamino)ethanol as the solvent, the metal-free phthalocyanine
2 was synthesized. The synthesis of metallophthalocyanines
3–
6 derived from 4-(quinolin-6-yloxy)phthalonitrile
1 were carried out by microwave irradiation. Aggregation properties of Pcs were investigated at different concentrations in chloroform, dimethylsulfoxide, dimethylformamide and water. The metal-free phthalocyanine
2 showed the aggregation in polar solvent DMSO, whereas in chloroform no aggregation was observed. The effect of the concentration on the aggregation properties of complexes
2,
3,
4 and
5 were studied in chloroform. No aggregation was demonstrated in chloroform from concentration between 1
×
10
−5 and 0.4
×
10
−5
M. The new compounds have been characterized by using elemental analysis, UV–Vis, IR,
1H NMR,
13C NMR and MS spectroscopic data. |
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ISSN: | 0379-6779 1879-3290 |
DOI: | 10.1016/j.synthmet.2010.12.035 |