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Derivatization and in situ metallation of phthalocyanines using click chemistry

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PERGAMON-ELSEVIER SCIENCE LTD

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10.1016/j.poly.2009.07.033

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Dialkyl (3,4-dicyanophenyl)propargylmalonates were prepared by the reaction of propargyl bromide and the potassium salt of dialkyl-3,4-dicyanophenylmalonates. A cyclotetramerization reaction was achieved in pentanol in the presence of DBU without protective/deprotective chemistry, affording the peripherally tetrasubstituted alkynyl phthalocyanines. Subsequently, in situ metallation and 'clicking' were employed for the first time as an efficient and quantitative route to tetratriazole-functionalized phthalocyanines. (c) 2009 Elsevier Ltd. All rights reserved.

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POLYHEDRON

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0277-5387

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