2018
DOI: 10.1134/s0036024418040271
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Crystallization and Simulation Studies in m-Dinitrobenzene–p-Chloroaniline Eutectic System

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“…The reported pK a values for the two amines of ED3A-OH are 9.9 and 5.4, the pK a of the first carboxylic acid is 2.4, and the remaining two carboxylic acids have pK a values less than 2. 49 As a result, at pH 2, the two amine groups of ED3A-OH are protonated, two of the carboxylates are deprotonated, and the third carboxylate is mostly protonated. In contrast, at pH 7, all three carboxylates and one of the amines are fully deprotonated.…”
Section: Resultsmentioning
confidence: 99%
“…The reported pK a values for the two amines of ED3A-OH are 9.9 and 5.4, the pK a of the first carboxylic acid is 2.4, and the remaining two carboxylic acids have pK a values less than 2. 49 As a result, at pH 2, the two amine groups of ED3A-OH are protonated, two of the carboxylates are deprotonated, and the third carboxylate is mostly protonated. In contrast, at pH 7, all three carboxylates and one of the amines are fully deprotonated.…”
Section: Resultsmentioning
confidence: 99%