Synthesis and Properties of Triazol-5-one Substituted Phthalocyanines by Microwave Irradiation
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Dosyalar
Tarih
2006
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Turkish Journal of Chemistry
Erişim Hakkı
Özet
Triazol-5-one substituted phthalocyanines were prepared quickly by the reaction of 4-nitrophthalonitrile with anhydrous metal salts in DBU (1,8-diazabicyclo[5,4,0]undec-7-ene) and DMAE (dimethylaminoethanol) by microwave irradiation. Microwave yields were higher than those of the conventional synthesis methods. All of these complexes are insoluble in polar solvents such as ethanol, ethyl acetate and chloroform. The characterization of the compounds was accomplished by elemental analysis, 1H NMR (for I and II), 13C NMR (for I and II), IR and UV-Vis spectral data. In addition, the structure of the starting material (I) was determined by single crystal diffraction.
Açıklama
Anahtar Kelimeler
Phthalocyanine, Microwave synthesis
Kaynak
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Scopus Q Değeri
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Künye
Kahveci, B., Şaşmaz, S., Özil, M., Kantar, C., Koşar, B., Büyükgüngör, O. "Synthesis and Properties of Triazol-5-one Substituted Phthalocyanines by Microwave Irradiation" Turkish Journal of Chemistry, 30 (2006) , 681 – 689.
