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Synthesis 2010(18): 3097-3104  
DOI: 10.1055/s-0030-1258178
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

Synthesis of Octaglycosylated Zinc(II) Phthalocyanines

Zafar Iqbala, Alexey Lyubimtseva,b, Timo Herrmannc, Michael Hanack*a, Thomas Ziegler*a
a Institut für Organische Chemie, Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany
Fax: +49(7071)295268; e-Mail: hanack@uni-tuebingen.de ; e-Mail: thomas.ziegler@uni-tuebingen.de;
b Ivanovo State University of Chemistry and Technology, Organic Chemistry Department, F. Engels Str. 7, 153460 Ivanovo, Russian Federation
c Medical and Natural Sciences Research Centre, Universität Tübingen, Ob dem Himmelreich 7, 72074 Tübingen, Germany
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Publikationsverlauf

Received 24 March 2010
Publikationsdatum:
16. Juli 2010 (online)

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Abstract

For the first time, octaglycosylated zinc(II) phthalocyanines in which the sugar part is protected by acetyl groups and the deprotected zinc(II) phthalocyanines were synthesized and characterized. The sugars glucose, galactose, lactose, cellobiose, and maltose are anomerically attached either via oxygen or sulfur to the phthalocyanine ring. The necessary starting materials for the syntheses of the phthalocyanines, the anomerically 4,5-diglycosylated phthalonitriles, were obtained by reacting the anomerically deprotected sugars containing OH and SH groups with 4,5-difluorophthalonitrile. The acetyl protected octaglycosylated phthalocyanines were obtained in yields between 55 and 78% by heating the anomerically 4,5-diglycosylated phthalonitriles in DMF with hexamethyldisilazane, p-toluenesulfonic acid, and zinc acetate. The acetyl groups in sugar moieties were removed to afford corresponding water­-soluble phthalocyanines.

Key words

phthalocyanines - octaglycosylated - zinc - structural isomers