Formation of anthocyanin ion-pairs. A co-pigmentation effect
Author(s) -
Paulo Figueiredo,
Fernando Piña
Publication year - 1994
Publication title -
journal of the chemical society. perkin transactions ii
Language(s) - English
Resource type - Journals
eISSN - 2050-8239
pISSN - 0300-9580
DOI - 10.1039/p29940000775
Subject(s) - chemistry , anthocyanin , anthocyanidin , ion , ionic bonding , salt (chemistry) , malvidin , photochemistry , inorganic chemistry , organic chemistry , cyanidin , food science
The influence of the addition of ionic salts (NaCl, NaBr, Nal, NaClO4) on anthocyanin equilibria is studied in this work. The effect of their addition is a colour enhancement through the formation of an ion-pair between the charged flavylium cation and the anion, which displaces the equilibria towards the coloured flavylium form. The ion-pair formation is an alternative model to that which suggests a preferable hydration of salt anions instead of the flavylium cation. Throughout this work two natural anthocyanins are studied (malvidin 3,5-diglucoside and malvidin 3-glucoside) as well as one anthocyanidin (malvidin). The thermal and photochemical stability of the ion-pairs formed is also examined.Experiments with a synthetic anthocyanin analogue (4′,7-dihydroxyflavylium chloride) which has photochromic properties are also described for comparison purposes.
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