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Syntheses and Functional Properties of Phthalocyanines

Metal phthalocyanine tetrasulfonic acids, metal phthalocyanine octacarboxylic acids, metal octakis(hexyloxymethyl)phthalocyanines, and metal anthraquinocyanines have been synthesized. Then, zinc bis(1,4-didecylbenzo)-bis(3,4-pyrido)porphyrazines, the cyclotetramerization products of a 1:1 mixture of...

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Autores principales: Sakamoto, Keiichi, Ohno-Okumura, Eiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445737/
http://dx.doi.org/10.3390/ma2031127
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author Sakamoto, Keiichi
Ohno-Okumura, Eiko
author_facet Sakamoto, Keiichi
Ohno-Okumura, Eiko
author_sort Sakamoto, Keiichi
collection PubMed
description Metal phthalocyanine tetrasulfonic acids, metal phthalocyanine octacarboxylic acids, metal octakis(hexyloxymethyl)phthalocyanines, and metal anthraquinocyanines have been synthesized. Then, zinc bis(1,4-didecylbenzo)-bis(3,4-pyrido)porphyrazines, the cyclotetramerization products of a 1:1 mixture of 3,6-didecylphthalonitrile and 3,4-dicyanopyridine, were synthesized. Futher, subphthalocyanine and its derivatives, with substituents such as thiobutyl and thiophenyl moieties were synthesized. Electrochemical measurements were performed on the abovementioned phthalocyanine derivatives and analogues in order to examine their electron transfer abilities and electrochemical reaction mechanisms in an organic solvent. Moreover, 1,4,8,11,15,18,22,25-octakis(thio-phenylmethyl)phthalocyanes were synthesized. The Q-bands of the latter compounds appeared in the near-infrared region. Furthermore, non-colored transparent films in the visible region can be produced.
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spelling pubmed-54457372017-07-28 Syntheses and Functional Properties of Phthalocyanines Sakamoto, Keiichi Ohno-Okumura, Eiko Materials (Basel) Article Metal phthalocyanine tetrasulfonic acids, metal phthalocyanine octacarboxylic acids, metal octakis(hexyloxymethyl)phthalocyanines, and metal anthraquinocyanines have been synthesized. Then, zinc bis(1,4-didecylbenzo)-bis(3,4-pyrido)porphyrazines, the cyclotetramerization products of a 1:1 mixture of 3,6-didecylphthalonitrile and 3,4-dicyanopyridine, were synthesized. Futher, subphthalocyanine and its derivatives, with substituents such as thiobutyl and thiophenyl moieties were synthesized. Electrochemical measurements were performed on the abovementioned phthalocyanine derivatives and analogues in order to examine their electron transfer abilities and electrochemical reaction mechanisms in an organic solvent. Moreover, 1,4,8,11,15,18,22,25-octakis(thio-phenylmethyl)phthalocyanes were synthesized. The Q-bands of the latter compounds appeared in the near-infrared region. Furthermore, non-colored transparent films in the visible region can be produced. Molecular Diversity Preservation International 2009-08-28 /pmc/articles/PMC5445737/ http://dx.doi.org/10.3390/ma2031127 Text en © 2009 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Sakamoto, Keiichi
Ohno-Okumura, Eiko
Syntheses and Functional Properties of Phthalocyanines
title Syntheses and Functional Properties of Phthalocyanines
title_full Syntheses and Functional Properties of Phthalocyanines
title_fullStr Syntheses and Functional Properties of Phthalocyanines
title_full_unstemmed Syntheses and Functional Properties of Phthalocyanines
title_short Syntheses and Functional Properties of Phthalocyanines
title_sort syntheses and functional properties of phthalocyanines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445737/
http://dx.doi.org/10.3390/ma2031127
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