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Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines

p-Coumaric acid (pCA) and trans-ferulic acid (TFA) were co-crystallised with 2-amino-4-picoline (2A4MP) and 2-amino-6-picoline (2A6MP) producing organic salts of (pCA(−))(2A4MP(+)) (1), (pCA(–) )(2A6MP(+)) (2) and (TFA(–) )(2A4MP(+))·([Formula: see text] H(2)O) (3). For salt 3, water was included in...

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Autores principales: Kamanda, Sosthene Nyomba, Jacobs, Ayesha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037943/
https://www.ncbi.nlm.nih.gov/pubmed/32050511
http://dx.doi.org/10.3390/molecules25030751
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author Kamanda, Sosthene Nyomba
Jacobs, Ayesha
author_facet Kamanda, Sosthene Nyomba
Jacobs, Ayesha
author_sort Kamanda, Sosthene Nyomba
collection PubMed
description p-Coumaric acid (pCA) and trans-ferulic acid (TFA) were co-crystallised with 2-amino-4-picoline (2A4MP) and 2-amino-6-picoline (2A6MP) producing organic salts of (pCA(−))(2A4MP(+)) (1), (pCA(–) )(2A6MP(+)) (2) and (TFA(–) )(2A4MP(+))·([Formula: see text] H(2)O) (3). For salt 3, water was included in the crystal structure fulfilling a bridging role. pCA formed a 1:1 salt with 2A4MP (Z’ = 1) and a 4:4 salt with 2A6MP (Z’ = 4). The thermal stability of the salts was determined using differential scanning calorimetry (DSC). Salt 2 had the highest thermal stability followed by salt 1 and salt 3. The salts were also characterised using Fourier transform infrared (FTIR) spectroscopy. Hirshfeld surface analysis was used to study the different intermolecular interactions in the three salts. Solvent-assisted grinding was also investigated in attempts to reproduce the salts.
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spelling pubmed-70379432020-03-10 Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines Kamanda, Sosthene Nyomba Jacobs, Ayesha Molecules Article p-Coumaric acid (pCA) and trans-ferulic acid (TFA) were co-crystallised with 2-amino-4-picoline (2A4MP) and 2-amino-6-picoline (2A6MP) producing organic salts of (pCA(−))(2A4MP(+)) (1), (pCA(–) )(2A6MP(+)) (2) and (TFA(–) )(2A4MP(+))·([Formula: see text] H(2)O) (3). For salt 3, water was included in the crystal structure fulfilling a bridging role. pCA formed a 1:1 salt with 2A4MP (Z’ = 1) and a 4:4 salt with 2A6MP (Z’ = 4). The thermal stability of the salts was determined using differential scanning calorimetry (DSC). Salt 2 had the highest thermal stability followed by salt 1 and salt 3. The salts were also characterised using Fourier transform infrared (FTIR) spectroscopy. Hirshfeld surface analysis was used to study the different intermolecular interactions in the three salts. Solvent-assisted grinding was also investigated in attempts to reproduce the salts. MDPI 2020-02-10 /pmc/articles/PMC7037943/ /pubmed/32050511 http://dx.doi.org/10.3390/molecules25030751 Text en © 2020 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
Kamanda, Sosthene Nyomba
Jacobs, Ayesha
Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title_full Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title_fullStr Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title_full_unstemmed Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title_short Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines
title_sort organic salts of p-coumaric acid and trans-ferulic acid with aminopicolines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037943/
https://www.ncbi.nlm.nih.gov/pubmed/32050511
http://dx.doi.org/10.3390/molecules25030751
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