What is Common and Different

Anthocyanins, anthocyanidins, 3-deoxyanthocyanins, and 3-deoxyanthocyanidins share five common chemical species in acidic media: flavylium cation, quinoidal base, hemiketal, and cis and trans chalcones. These species are reversibly interconnected by four chemical reactions: proton transfer, hydration, tautomerization, and isomerization. The absence of a hydroxyl group or glycoside at position 3 of the flavylium cation in 3-deoxy species substantially alters their thermodynamic and kinetic properties compared to those of anthocyanins. This study compared these properties between anthocyanins and 3-deoxy species and investigated the chemistry and photochemistry of luteolinidin using an updated mathematical model. The extension of the study to basic media (holistic approach) revealed slower OH- nucleophilic addition in luteolinidin, consequently prolonging its color retention in comparison to anthocyanins. Furthermore, luteolinidin exhibit significantly slower degradation rates. While anthocyanins generally lack significant photochemistry, 3-deoxy species display efficient photochromism, presenting promising possibilities for diverse applications.

Publication Details

Journal
Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Published
2025-02-22
Primary Topic
Chemistry and Chemical Engineering
Type
article
Field-Weighted Citation Impact
0.00
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article

What is Common and Different

Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Chemistry and Chemical Engineering
article

What is Common and Different

article en

Abstract

Anthocyanins, anthocyanidins, 3-deoxyanthocyanins, and 3-deoxyanthocyanidins share five common chemical species in acidic media: flavylium cation, quinoidal base, hemiketal, and cis and trans chalcones. These species are reversibly interconnected by four chemical reactions: proton transfer, hydration, tautomerization, and isomerization. The absence of a hydroxyl group or glycoside at position 3 of the flavylium cation in 3-deoxy species substantially alters their thermodynamic and kinetic properties compared to those of anthocyanins. This study compared these properties between anthocyanins and 3-deoxy species and investigated the chemistry and photochemistry of luteolinidin using an updated mathematical model. The extension of the study to basic media (holistic approach) revealed slower OH- nucleophilic addition in luteolinidin, consequently prolonging its color retention in comparison to anthocyanins. Furthermore, luteolinidin exhibit significantly slower degradation rates. While anthocyanins generally lack significant photochemistry, 3-deoxy species display efficient photochromism, presenting promising possibilities for diverse applications.

Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Openalex Percentile: Top 41%
Chemistry and Chemical Engineering
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