Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/8664
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dc.contributor.authorKamanda, Sosthene Nyombaen_US
dc.contributor.authorJacobs, Ayeshaen_US
dc.date.accessioned2022-07-18T12:31:13Z-
dc.date.available2022-07-18T12:31:13Z-
dc.date.issued2020-
dc.identifier.citationKamanda, S.N. & Jacobs, A. 2020. Organic salts of p-coumaric acid and trans-ferulic acid with aminopicolines. Molecules, 25(3): 1-11. [https://doi.org/10.3390/molecules25030751]en_US
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/11189/8664-
dc.description.abstractp-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), (pCA̶ )(2A6MP+) (2) and (TFA̶ )(2A4MP+)·( 32 H2O) (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 saltsen_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofMoleculesen_US
dc.subjectp-Coumaric aciden_US
dc.subjecttrans-ferulic aciden_US
dc.subjectorganic salsen_US
dc.subjecthydroxycinnamic acidsen_US
dc.subjectmulticomponent crystalsen_US
dc.titleOrganic salts of p-coumaric acid and trans-ferulic acid with aminopicolinesen_US
dc.identifier.doihttps://doi.org/10.3390/molecules25030751-
dc.typeArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
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