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. 2020 Feb 25;9(3):189. doi: 10.3390/antiox9030189

Table 5.

PA, ETE and ΔH of starting materials and fragments of compounds 1 and 2.

Molecule PA (kJ/mol) ETE (kJ/mol) ΔH (kJ/mol)
Compound 1 451 1017 1468
Starting material Vanillin (Y) 120 386 1518 a
Fragment 1 4-(Aminomethyl)-2-methoxyphenol (Y’) 151 335 1458 b
Fragment 2 4-Methyl-2-methoxyphenol (Y”) 155 328 1449 c
Compound 2 448 984 1432
Starting Material Syringaldehyde (X) 118 371 1484 d
Fragment 1 4-(Aminomethyl)-2,6-dimethoxyphenol (X’) 152 317 1424 e
Fragment 2 4-Methyl-2,6-dimethoxyphenol (X”) 155 310 1413 f

a ΔH = 3 equiv. PA (Y) + 3 equiv. ETE (Y), b ΔH = 3 equiv. PA (Y’) + 3 equiv. ETE (Y’), c ΔH = 3 equiv. PA (Y”) + 3 equiv. ETE (Y”), d ΔH = 2 equiv. PA (X) + 1 equiv. PA (Y) + 2 equiv. ETE (X) + 1 equiv. ETE (Y), e ΔH = 2 equiv. PA (X’) + 1 equiv. PA (Y’) + 2 equiv. ETE (X’) + 1 equiv. ETE (Y’), f ΔH = 2 equiv. PA (X”) + 1 equiv. PA (Y”) + 2 equiv. ETE (X”) + 1 equiv. ETE (Y”).