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Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates

We report of the interactions between four amino acids lysine (Lys), arginine (Arg), histidine (His), and phenylalanine (Phe) with the J-aggregates of the protonated 5,10,15,20-tetrakis(4-sulfonatophenyl)-porphyrin H(4)TPPS. Several aspects of these self-assembled systems have been analyzed: (i) the...

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Autores principales: Randazzo, Rosalba, Gaeta, Massimiliano, Gangemi, Chiara Maria Antonietta, Fragalà, Maria Elena, Purrello, Roberto, D’Urso, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337589/
https://www.ncbi.nlm.nih.gov/pubmed/30591641
http://dx.doi.org/10.3390/molecules24010084
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author Randazzo, Rosalba
Gaeta, Massimiliano
Gangemi, Chiara Maria Antonietta
Fragalà, Maria Elena
Purrello, Roberto
D’Urso, Alessandro
author_facet Randazzo, Rosalba
Gaeta, Massimiliano
Gangemi, Chiara Maria Antonietta
Fragalà, Maria Elena
Purrello, Roberto
D’Urso, Alessandro
author_sort Randazzo, Rosalba
collection PubMed
description We report of the interactions between four amino acids lysine (Lys), arginine (Arg), histidine (His), and phenylalanine (Phe) with the J-aggregates of the protonated 5,10,15,20-tetrakis(4-sulfonatophenyl)-porphyrin H(4)TPPS. Several aspects of these self-assembled systems have been analyzed: (i) the chiral transfer process; (ii) the hierarchical effects leading to the aggregates formation; and, (iii) the influence of the amino acid concentrations on both transferring and storing chiral information. We have demonstrated that the efficient control on the J-aggregates chirality is obtained when all amino acids are tested and that the chirality transfer process is under hierarchical control. Finally, the chiral porphyrin aggregates obtained exhibit strong chiral inertia.
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spelling pubmed-63375892019-01-25 Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates Randazzo, Rosalba Gaeta, Massimiliano Gangemi, Chiara Maria Antonietta Fragalà, Maria Elena Purrello, Roberto D’Urso, Alessandro Molecules Article We report of the interactions between four amino acids lysine (Lys), arginine (Arg), histidine (His), and phenylalanine (Phe) with the J-aggregates of the protonated 5,10,15,20-tetrakis(4-sulfonatophenyl)-porphyrin H(4)TPPS. Several aspects of these self-assembled systems have been analyzed: (i) the chiral transfer process; (ii) the hierarchical effects leading to the aggregates formation; and, (iii) the influence of the amino acid concentrations on both transferring and storing chiral information. We have demonstrated that the efficient control on the J-aggregates chirality is obtained when all amino acids are tested and that the chirality transfer process is under hierarchical control. Finally, the chiral porphyrin aggregates obtained exhibit strong chiral inertia. MDPI 2018-12-27 /pmc/articles/PMC6337589/ /pubmed/30591641 http://dx.doi.org/10.3390/molecules24010084 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Randazzo, Rosalba
Gaeta, Massimiliano
Gangemi, Chiara Maria Antonietta
Fragalà, Maria Elena
Purrello, Roberto
D’Urso, Alessandro
Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title_full Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title_fullStr Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title_full_unstemmed Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title_short Chiral Recognition of L- and D- Amino Acid by Porphyrin Supramolecular Aggregates
title_sort chiral recognition of l- and d- amino acid by porphyrin supramolecular aggregates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337589/
https://www.ncbi.nlm.nih.gov/pubmed/30591641
http://dx.doi.org/10.3390/molecules24010084
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