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Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons

The solubilization capacity of a series of sustainable phenylalanine-derived surface-active ionic liquids (SAILs) was evaluated towards polycyclic aromatic hydrocarbons—naphthalene, anthracene and pyrene. The key physico-chemical parameters of the studied systems (critical micelle concentration, spe...

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Autores principales: Kapitanov, Illia V., Sudheer, Surya M., Yadav, Toshikee, Ghosh, Kallol K., Gathergood, Nicholas, Gupta, Vijai K., Karpichev, Yevgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222739/
https://www.ncbi.nlm.nih.gov/pubmed/37241924
http://dx.doi.org/10.3390/molecules28104185
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author Kapitanov, Illia V.
Sudheer, Surya M.
Yadav, Toshikee
Ghosh, Kallol K.
Gathergood, Nicholas
Gupta, Vijai K.
Karpichev, Yevgen
author_facet Kapitanov, Illia V.
Sudheer, Surya M.
Yadav, Toshikee
Ghosh, Kallol K.
Gathergood, Nicholas
Gupta, Vijai K.
Karpichev, Yevgen
author_sort Kapitanov, Illia V.
collection PubMed
description The solubilization capacity of a series of sustainable phenylalanine-derived surface-active ionic liquids (SAILs) was evaluated towards polycyclic aromatic hydrocarbons—naphthalene, anthracene and pyrene. The key physico-chemical parameters of the studied systems (critical micelle concentration, spectral properties, solubilization parameters) were determined, analyzed and compared with conventional cationic surfactant, CTABr. For all studied PAH solubilization capacity increases with extension of alkyl chain length of PyPheOC(n) SAILs reaching the values comparable to CTABr for SAILs with n = 10–12. A remarkable advantage of the phenylalanine-derived SAILs PyPheOC(n) and PyPheNHC(n) is a possibility to cleave enzymatically ester and/or amide bonds under mild conditions, to separate polycyclic aromatic hydrocarbons in situ. A series of immobilized enzymes was tested to determine the most suitable candidates for tunable decomposition of SAILs. The decomposition pathway could be adjusted depending on the choice of the enzyme system, reaction conditions, and selection of SAILs type. The evaluated systems can provide selective cleavage of the ester and amide bond and help to choose the optimal decomposition method of SAILs for enzymatic recycling of SAILs transformation products or as a pretreatment towards biological mineralization. The concept of a possible practical application of studied systems for PAHs solubilization/separation was also discussed focusing on sustainability and a green chemistry approach.
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spelling pubmed-102227392023-05-28 Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons Kapitanov, Illia V. Sudheer, Surya M. Yadav, Toshikee Ghosh, Kallol K. Gathergood, Nicholas Gupta, Vijai K. Karpichev, Yevgen Molecules Article The solubilization capacity of a series of sustainable phenylalanine-derived surface-active ionic liquids (SAILs) was evaluated towards polycyclic aromatic hydrocarbons—naphthalene, anthracene and pyrene. The key physico-chemical parameters of the studied systems (critical micelle concentration, spectral properties, solubilization parameters) were determined, analyzed and compared with conventional cationic surfactant, CTABr. For all studied PAH solubilization capacity increases with extension of alkyl chain length of PyPheOC(n) SAILs reaching the values comparable to CTABr for SAILs with n = 10–12. A remarkable advantage of the phenylalanine-derived SAILs PyPheOC(n) and PyPheNHC(n) is a possibility to cleave enzymatically ester and/or amide bonds under mild conditions, to separate polycyclic aromatic hydrocarbons in situ. A series of immobilized enzymes was tested to determine the most suitable candidates for tunable decomposition of SAILs. The decomposition pathway could be adjusted depending on the choice of the enzyme system, reaction conditions, and selection of SAILs type. The evaluated systems can provide selective cleavage of the ester and amide bond and help to choose the optimal decomposition method of SAILs for enzymatic recycling of SAILs transformation products or as a pretreatment towards biological mineralization. The concept of a possible practical application of studied systems for PAHs solubilization/separation was also discussed focusing on sustainability and a green chemistry approach. MDPI 2023-05-19 /pmc/articles/PMC10222739/ /pubmed/37241924 http://dx.doi.org/10.3390/molecules28104185 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kapitanov, Illia V.
Sudheer, Surya M.
Yadav, Toshikee
Ghosh, Kallol K.
Gathergood, Nicholas
Gupta, Vijai K.
Karpichev, Yevgen
Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title_full Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title_fullStr Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title_full_unstemmed Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title_short Sustainable Phenylalanine-Derived SAILs for Solubilization of Polycyclic Aromatic Hydrocarbons
title_sort sustainable phenylalanine-derived sails for solubilization of polycyclic aromatic hydrocarbons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222739/
https://www.ncbi.nlm.nih.gov/pubmed/37241924
http://dx.doi.org/10.3390/molecules28104185
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