
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), (pCA̶ )(2A6MP+) (2) and (TFA̶ )(2A4MP+)·( 3 2 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 salts.
p-coumaric acid, multicomponent crystals, Calorimetry, Differential Scanning, Coumaric Acids, Spectrophotometry, Infrared, Organic chemistry, Hydrogen Bonding, hydroxycinnamic acids, Crystallography, X-Ray, Article, organic sals, QD241-441, Picolines, Spectroscopy, Fourier Transform Infrared, Solvents, Salts, Propionates, trans-ferulic acid, Crystallization
p-coumaric acid, multicomponent crystals, Calorimetry, Differential Scanning, Coumaric Acids, Spectrophotometry, Infrared, Organic chemistry, Hydrogen Bonding, hydroxycinnamic acids, Crystallography, X-Ray, Article, organic sals, QD241-441, Picolines, Spectroscopy, Fourier Transform Infrared, Solvents, Salts, Propionates, trans-ferulic acid, Crystallization
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