Anthocyanin–aluminium and –gallium complexes in aqueous solution
Main Author: | |
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Publication Date: | 1997 |
Other Authors: | , , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
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RCAAP |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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1833602985233481728 |