Anthocyanin–aluminium and –gallium complexes in aqueous solution

Bibliographic Details
Main Author: Elhabiri, Mourad
Publication Date: 1997
Other Authors: Figueiredo, Paulo, Toki, Kenjiro, Saito, Norio, Brouillard, Raymond
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10884/501
Summary: Complexation of aluminium and gallium ions with synthetic anthocyanin models and natural anthocyanins extracted from the blue flowers of Evolvulus pilosus cv ‘Blue Daze’ and the violet flowers of Matthiola incana has been thoroughly investigated in aqueous solution. From UV–VIS spectroscopic data collected at pH 2–5, the presence of complexes, involving not only the coloured forms but also the colourless forms of the pigments is demonstrated. A theoretical treatment is developed for the calculation of the corresponding stability constants. The pigments studied throughout this work can be divided into two series, one sharing a cyanidin chromophore and the other a delphinidin one. Within both series, individual pigments are distinguished according to the degree and type of glycosylation and/or acylation. Intramolecular effects such as copigmentation of anthocyanin–aluminium complexes and the effect of the presence of a malonyl group on the formation of those complexes are discussed. These results are important to plant pigmentation and, for instance, a narrow pH domain in which colour amplification due to complexation is at a maximum has been found.
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spelling Anthocyanin–aluminium and –gallium complexes in aqueous solutionAnthocyaninMetalic complexationAluminiumGalliumComplexation of aluminium and gallium ions with synthetic anthocyanin models and natural anthocyanins extracted from the blue flowers of Evolvulus pilosus cv ‘Blue Daze’ and the violet flowers of Matthiola incana has been thoroughly investigated in aqueous solution. From UV–VIS spectroscopic data collected at pH 2–5, the presence of complexes, involving not only the coloured forms but also the colourless forms of the pigments is demonstrated. A theoretical treatment is developed for the calculation of the corresponding stability constants. The pigments studied throughout this work can be divided into two series, one sharing a cyanidin chromophore and the other a delphinidin one. Within both series, individual pigments are distinguished according to the degree and type of glycosylation and/or acylation. Intramolecular effects such as copigmentation of anthocyanin–aluminium complexes and the effect of the presence of a malonyl group on the formation of those complexes are discussed. These results are important to plant pigmentation and, for instance, a narrow pH domain in which colour amplification due to complexation is at a maximum has been found.2012-03-06T15:56:59Z2012-03-061997-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10884/501http://hdl.handle.net/10884/501engJ. Chem. Soc., Perkin Trans. 2, 1997, 355-362Elhabiri, MouradFigueiredo, PauloToki, KenjiroSaito, NorioBrouillard, Raymondinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-05-15T17:40:44Zoai:repositorio-cientifico.uatlantica.pt:10884/501Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T07:27:13.348594Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Anthocyanin–aluminium and –gallium complexes in aqueous solution
title Anthocyanin–aluminium and –gallium complexes in aqueous solution
spellingShingle Anthocyanin–aluminium and –gallium complexes in aqueous solution
Elhabiri, Mourad
Anthocyanin
Metalic complexation
Aluminium
Gallium
title_short Anthocyanin–aluminium and –gallium complexes in aqueous solution
title_full Anthocyanin–aluminium and –gallium complexes in aqueous solution
title_fullStr Anthocyanin–aluminium and –gallium complexes in aqueous solution
title_full_unstemmed Anthocyanin–aluminium and –gallium complexes in aqueous solution
title_sort Anthocyanin–aluminium and –gallium complexes in aqueous solution
author Elhabiri, Mourad
author_facet Elhabiri, Mourad
Figueiredo, Paulo
Toki, Kenjiro
Saito, Norio
Brouillard, Raymond
author_role author
author2 Figueiredo, Paulo
Toki, Kenjiro
Saito, Norio
Brouillard, Raymond
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Elhabiri, Mourad
Figueiredo, Paulo
Toki, Kenjiro
Saito, Norio
Brouillard, Raymond
dc.subject.por.fl_str_mv Anthocyanin
Metalic complexation
Aluminium
Gallium
topic Anthocyanin
Metalic complexation
Aluminium
Gallium
description Complexation of aluminium and gallium ions with synthetic anthocyanin models and natural anthocyanins extracted from the blue flowers of Evolvulus pilosus cv ‘Blue Daze’ and the violet flowers of Matthiola incana has been thoroughly investigated in aqueous solution. From UV–VIS spectroscopic data collected at pH 2–5, the presence of complexes, involving not only the coloured forms but also the colourless forms of the pigments is demonstrated. A theoretical treatment is developed for the calculation of the corresponding stability constants. The pigments studied throughout this work can be divided into two series, one sharing a cyanidin chromophore and the other a delphinidin one. Within both series, individual pigments are distinguished according to the degree and type of glycosylation and/or acylation. Intramolecular effects such as copigmentation of anthocyanin–aluminium complexes and the effect of the presence of a malonyl group on the formation of those complexes are discussed. These results are important to plant pigmentation and, for instance, a narrow pH domain in which colour amplification due to complexation is at a maximum has been found.
publishDate 1997
dc.date.none.fl_str_mv 1997-01-01T00:00:00Z
2012-03-06T15:56:59Z
2012-03-06
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dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10884/501
http://hdl.handle.net/10884/501
url http://hdl.handle.net/10884/501
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv J. Chem. Soc., Perkin Trans. 2, 1997, 355-362
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