Literature DB >> 21842035

Chemistry and applications of flavylium compounds: a handful of colours.

Fernando Pina1, Maria J Melo, César A T Laia, A Jorge Parola, João C Lima.   

Abstract

Flavylium compounds are versatile molecules that comprise anthocyanins, the ubiquitous colorants used by Nature to confer colour to most flowers and fruits. They have found a wide range of applications in human technology, from the millenary colour paints described by the Roman architect Vitruvius, to their use as food additives, combining colour and antioxidant effects, and even as light absorbers in solar cells aiming at a greener solar energy conversion. Their rich complexity derives in part from their ability to switch between a variety of species (flavylium cations, neutral quinoidal bases, hemiketals and chalcones, and negatively charged phenolates) by means of external stimuli, such as pH, temperature and light. This critical review describes (i) the historical advancements in the understanding of the equilibria of their chemical reaction networks; (ii) their thermodynamics and kinetics; (iii) the mechanisms underlying their colour development, such as co-pigmentation and host-guest interactions; (iv) the photophysics and photochemistry that lead to photochromism; and (v) applications in solar cells, models for optical memories, photochromic soft materials such as ionic liquids and gels, and their properties in solid state materials (274 references).

Entities:  

Year:  2011        PMID: 21842035     DOI: 10.1039/c1cs15126f

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  33 in total

1.  Metalloradical approach to 2H-chromenes.

Authors:  Nanda D Paul; Sutanuva Mandal; Matthias Otte; Xin Cui; X Peter Zhang; Bas de Bruin
Journal:  J Am Chem Soc       Date:  2014-01-08       Impact factor: 15.419

2.  Nickel-catalyzed cross-coupling of chromene acetals and boronic acids.

Authors:  Thomas J A Graham; Abigail G Doyle
Journal:  Org Lett       Date:  2012-03-02       Impact factor: 6.005

3.  Preparation and pH Controlled Release of Fe3O4/Anthocyanin Magnetic Biocomposites.

Authors:  Xizhi Jiang; Qingbao Guan; Min Feng; Mengyang Wang; Nina Yan; Min Wang; Lei Xu; Zhongzheng Gui
Journal:  Polymers (Basel)       Date:  2019-12-12       Impact factor: 4.329

4.  Chlorophyll- and anthocyanin-rich cell organelles affect light scattering in apple skin.

Authors:  Stefan A Lohner; Konni Biegert; Ansgar Hohmann; Roy McCormick; Alwin Kienle
Journal:  Photochem Photobiol Sci       Date:  2022-01-09       Impact factor: 3.982

Review 5.  Biosynthesis and regulation of anthocyanin pathway genes.

Authors:  L Sunil; Nandini P Shetty
Journal:  Appl Microbiol Biotechnol       Date:  2022-02-16       Impact factor: 4.813

6.  Analogs of Natural 3-Deoxyanthocyanins: O-Glucosides of the 4',7-Dihydroxyflavylium Ion and the Deep Influence of Glycosidation on Color.

Authors:  Nuno Basílio; Sheiraz Al Bittar; Nathalie Mora; Olivier Dangles; Fernando Pina
Journal:  Int J Mol Sci       Date:  2016-10-20       Impact factor: 5.923

7.  p-Hydroxyphenyl-pyranoanthocyanins: An Experimental and Theoretical Investigation of Their Acid-Base Properties and Molecular Interactions.

Authors:  Anna Vallverdú-Queralt; Michal Biler; Emmanuelle Meudec; Christine Le Guernevé; Aude Vernhet; Jean-Paul Mazauric; Jean-Luc Legras; Michèle Loonis; Patrick Trouillas; Véronique Cheynier; Olivier Dangles
Journal:  Int J Mol Sci       Date:  2016-11-05       Impact factor: 5.923

8.  Oral interactions between a green tea flavanol extract and red wine anthocyanin extract using a new cell-based model: insights on the effect of different oral epithelia.

Authors:  Susana Soares; Sónia Soares; Elsa Brandão; Carlos Guerreiro; Nuno Mateus; Victor de Freitas
Journal:  Sci Rep       Date:  2020-07-28       Impact factor: 4.379

9.  Synthetic anthocyanidins and their antioxidant properties.

Authors:  Homar S Barcena; Peishan Chen; Abraham Tuachi
Journal:  Springerplus       Date:  2015-09-17

10.  Extending the Study of the 6,8 Rearrangement in Flavylium Compounds to Higher pH Values: Interconversion between 6-Bromo and 8-Bromo-apigeninidin.

Authors:  Luís M Cruz; Nuno M Basílio; Victor A de Freitas; João C Lima; Fernando J Pina
Journal:  ChemistryOpen       Date:  2016-02-25       Impact factor: 2.911

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