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Synthesis and NMR Studies of a Single Isomer of an Alkynyl Substituted Binuclear Phthalocyanine

✍ Scribed by Hiroaki Isago; Dmitri S. Terekhov; Clifford C. Leznoff


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
149 KB
Volume
01
Category
Article
ISSN
1088-4246

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✦ Synopsis


By a mixed condensation of 1,3-bis(3β€³,4β€³-dicyanophenoxy)-2-ethyl-2-methylpropane with a large amount of 4,5-bis(3,3-dimethyl-1-butynyl)phthalonitrile, 1,3-bis-2β€³-(9β€³,10β€³,16β€³,17β€³,23β€³,24β€³-hexakis(3β€³,3β€³-dimethyl-1β€³-butynyl)phthalocyaninoxyl)-2-ethyl-2-methylpropane, was synthesized as a binuclear phthalocyanine having a single isomer. NMR studies at various temperatures and concentrations suggested that the interactions between the phthalocyanine macrocycles were dominated by intermolecular aggregation at lower temperatures or high concentrations whereas intramolecular aggregation was predominant at higher temperatures or lower concentrations.


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