The synthesis of single- and double-decked anthracenyl functionalized ruthenium(II) phthalocyanine complexes has been achieved through a controlled electrophilic aromatic substitution reaction of the free unsubstituted ruthenium(II) phthalocyanine with preformed 9-bromo-10-(2,3-dimethylacrylic acid)-anthracene and/or 9-bromo-10-(2,3-dimethylacrylic acid)-dianthracene using 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as catalyst. The complexes were characterized by IR, UV-Vis, fluorescence, 1H, 13C NMR, and elemental analyses. A dimeric complex (C 3 R ′ ′ R u P c, where R ′ ′ is 9-dianthracenyl-10-(2,3-dimethylacrylic acid), obtained as the major product of the dianthracenyl-substituted ruthenium phthalocyanine complex displays a strong near-infrared visible absorption band wavelength maxima at 1027 nm (ε = 5.47 × 10 3 M-1 cm-1), with an interesting photoluminescent and electroredox active properties. © 2014 Adewale O. Adeloye and Peter A. Ajibade.
CITATION STYLE
Adeloye, A. O., & Ajibade, P. A. (2014). Synthesis, characterization, electrochemistry, and spectroscopic properties of some anthracenyl functionalized phthalocyanine complexes of ruthenium(II). Journal of Chemistry, 2014. https://doi.org/10.1155/2014/257206
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