Ultrasonically induced phthalocyanine degradation: decolouration vs. metal release.

The ultrasonically induced degradations of nickel(II) 2,9,16,23-tetraphenoxy-29H, 31H-phthalocyanine and vanadyl 2,9,16,23-tetraphenoxy-29H, 31H-phthalocyanine in a biphasic system consisting of chloroform and water are investigated. Decolourisation of the organic phase containing the metallo-phthal...

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Bibliographic Details
Main Authors: Banks, C, Wylie, A, Compton, R
Format: Journal article
Language:English
Published: 2004
Description
Summary:The ultrasonically induced degradations of nickel(II) 2,9,16,23-tetraphenoxy-29H, 31H-phthalocyanine and vanadyl 2,9,16,23-tetraphenoxy-29H, 31H-phthalocyanine in a biphasic system consisting of chloroform and water are investigated. Decolourisation of the organic phase containing the metallo-phthalocyanines is found to occur rapidly (approximately minutes for 8 ml of ca. 5 microM solution). Analysis of the aqueous solute via ICP-OES, reveals significant amounts of the released nickel ultimately transfers into the aqueous phase but at a rate much slower than that of decolourisation, whereas the vanadium remains within the organic phase suggesting only partial degradation despite efficient decolourisation.