2015
DOI: 10.1134/s1070363215100205
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Phthalocyanines with peripheral azo chromophores

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Cited by 4 publications
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“…It was also noted that FT-IR spectra of sulfonic acids are more diffuse compared to the initial ones, as was previously noted for phthalocyanines sulfonic acids. [20][21] The solubility in the synthesized phthalocyanines (4-7) in organic solvents or aqueous-alkaline solutions allowed us to study their spectral characteristics. So, electronic absorbance spectra of all synthesized complexes are characterized by intense absorption in the wavelength region of 660-680 nm, caused by the π-π* electronic transition in the main conjugation circuit of the phthalocyanine ring.…”
Section: Scheme 4 Sulfonation Of Phthalocyanine Complexesmentioning
confidence: 99%
“…It was also noted that FT-IR spectra of sulfonic acids are more diffuse compared to the initial ones, as was previously noted for phthalocyanines sulfonic acids. [20][21] The solubility in the synthesized phthalocyanines (4-7) in organic solvents or aqueous-alkaline solutions allowed us to study their spectral characteristics. So, electronic absorbance spectra of all synthesized complexes are characterized by intense absorption in the wavelength region of 660-680 nm, caused by the π-π* electronic transition in the main conjugation circuit of the phthalocyanine ring.…”
Section: Scheme 4 Sulfonation Of Phthalocyanine Complexesmentioning
confidence: 99%