Water-Soluble Colorimetric Amino[bis(ethanesulfonate)] Azobenzene pH Indicators: A UV–Vis Absorption, DFT, and (1)H–(15)N NMR Spectroscopy Study

[Image: see text] Water-soluble azobenzene derivatives containing amino[bis(ethanesulfonate)] groups are demonstrated as colorful pH indicators in water and on filter paper. Vibrant color changes were observed from yellow/orange to pink between pH 1 and 4, which are attributed to an intramolecular c...

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Detalles Bibliográficos
Autores principales: Cardona, Maria A., Makuc, Damjan, Szaciłowski, Konrad, Plavec, Janez, Magri, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644513/
https://www.ncbi.nlm.nih.gov/pubmed/31457862
http://dx.doi.org/10.1021/acsomega.7b00887
Descripción
Sumario:[Image: see text] Water-soluble azobenzene derivatives containing amino[bis(ethanesulfonate)] groups are demonstrated as colorful pH indicators in water and on filter paper. Vibrant color changes were observed from yellow/orange to pink between pH 1 and 4, which are attributed to an intramolecular charge-transfer mechanism. The pK(a)s of the indicators range from 2.1 to 2.6. (1)H/(1)H–(15)N NMR studies in deuterium oxide reveal that the protonation of the azobenzene pH indicators occurs predominantly at the β-azo nitrogen atom, in agreement with the density functional theory calculations. Excellent selectivity for protons was confirmed in water over common biologically relevant metal ions. Studies in methanol, however, indicate that the pH indicator with a methoxy group ortho to the amino[bis(ethanesulfonate)] group facilitates the selective coordination of Cu(2+) with a binding constant pβ(Cu2+) of 4.6 ± 0.1. The indicators complement the existing library of azobenzene indicator dyes and may be useful for measuring the environmental pH at higher proton concentrations.