Chemistry and photochemistry of novel aromatic spiroketals derived from 2,6-bis(5-bromo-2-hydroxybenzylidene) cyclohexanone

Natural colorants such as flavylium and xanthylium derivatives have attracted considerable interest in the last decades due to their potential health effects and replacement of synthetic pigments. In addition, these type of compounds exhibit versatile photochromic properties by switching from a vari...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Deveseleanu-Corîci Livia
Şova Sergiu
Badea Valentin
Costisor Otilia
Cseh Liliana
Testületi szerző: International Symposium on Analytical and Environmental Problems (22.) (2016) (Szeged)
Dokumentumtípus: Könyv része
Megjelent: 2016
Sorozat:Proceedings of the International Symposium on Analytical and Environmental Problems 22
Kulcsszavak:Kémia - előadáskivonat
Online Access:http://acta.bibl.u-szeged.hu/56054
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245 1 0 |a Chemistry and photochemistry of novel aromatic spiroketals derived from 2,6-bis(5-bromo-2-hydroxybenzylidene) cyclohexanone  |h [elektronikus dokumentum] /  |c  Deveseleanu-Corîci Livia 
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490 0 |a Proceedings of the International Symposium on Analytical and Environmental Problems  |v 22 
520 3 |a Natural colorants such as flavylium and xanthylium derivatives have attracted considerable interest in the last decades due to their potential health effects and replacement of synthetic pigments. In addition, these type of compounds exhibit versatile photochromic properties by switching from a variety of colourswhen submitted to different external stimuli[1-3]. The aim of the present work was to design novel photochromic systems based on xanthylium derivatives. Therefore, we have synthesized and characterized 2,6-bis(5-bromo-2- hydroxybenzylidene)cyclohexanone. The network of chemical reactions when submitted to light and different pH values has been investigated. A new colorless compound 3,11-dibromo7,8-dihydro-6H-chromeno[3,2-d]xanthenes(Scheme 1) isolated from the equilibrated solution of trans-chalcone specie in methanolhave been isolated and fully characterized by NMR and X-ray diffraction. The rate of the reaction increased when the solution of trans-chalcone was exposed to sunlight. The spiroketal form was stable at in neutral and basic conditions, while at low pH values it converts into xantylium cationic form. 
695 |a Kémia - előadáskivonat 
700 0 1 |a Şova Sergiu  |e aut 
700 0 1 |a Badea Valentin  |e aut 
700 0 1 |a Costisor Otilia  |e aut 
700 0 1 |a Cseh Liliana  |e aut 
710 |a International Symposium on Analytical and Environmental Problems (22.) (2016) (Szeged) 
856 4 0 |u http://acta.bibl.u-szeged.hu/56054/1/proceedings_of_isaep_2016_124.pdf  |z Dokumentum-elérés