JOURNAL ARTICLE

Synthesis, photochemical and photophysical properties of novel unsymmetrically substituted zinc(II) phthalocyanines

Shaya Y. Al‐Raqa

Year: 2006 Journal:   Journal of Porphyrins and Phthalocyanines Vol: 10 (01)Pages: 55-62   Publisher: World Scientific

Abstract

The synthesis of three novel unsymmetrical free base, zinc(II) phthalocyanine derivatives obtained from 3,6-di-(thiophen-3-yl)phthalonitrile and 3,6-didecylphthalonitrile are described. The synthesis of novel 3,6-substituted phthalonitriles bearing heteroaromatic derivatives were achieved through Suzuki-coupling reaction by treatment of 3,6-di(trifluoromethanesulfonyloxy)phthalonitriles and heteroaromatic boronic acids. Two of the newly synthesized complexes showed a high efficiency against a model biological substrate, such as N-acetyl-L-tryptophanamide NATA, and shows a high singlet oxygen quantum yield.

Keywords:
Chemistry Phthalonitrile Zinc Phthalocyanine Singlet oxygen Suzuki reaction Quantum yield Substrate (aquarium) Yield (engineering) Photochemistry Boronic acid Combinatorial chemistry Coupling reaction Polymer chemistry Organic chemistry Aryl Fluorescence Oxygen Catalysis

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Citation History

Topics

Porphyrin and Phthalocyanine Chemistry
Physical Sciences →  Materials Science →  Materials Chemistry
Photodynamic Therapy Research Studies
Health Sciences →  Medicine →  Pulmonary and Respiratory Medicine
Oxidative Organic Chemistry Reactions
Physical Sciences →  Chemistry →  Organic Chemistry
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