Insight into the deprotonation at the half-equivalence point of (thio)amido-benzimidazoles in the presence of anions
2017
Three crystallographic structures highlight the acid–base half-equivalence point of hydrogen-bond donor (thio)amido-benzimidazoles induced by fluoride or benzoate salts with concomitant hydrogen-bonding and deprotonation as a merged synergic process.
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