Direct and Reversible Esterification of a Phosphonic Acid under Ambient Conditions through a Dissociative Mechanism

Abstract We report the synthesis of 1-dimethylaminonaphthyl-8-phosphonic acid, which, in contrast with typical phosphonic acids, undergoes spontaneous condensation with alcohols to give monoesters under ambient conditions. The selectivity and reversibility of the reaction suggest that it occurs through a dissociative mechanism, inaccessible to typical phosphonic acids.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-09-29
DOI
https://doi.org/10.1021/acs.inorgchem.6c03183
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
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article

Direct and Reversible Esterification of a Phosphonic Acid under Ambient Conditions through a Dissociative Mechanism

Marc‐André Légaré, Yuxiang Wei, Christina K. McCabe
Inorganic Chemistry
Organophosphorus compounds synthesis
article

Direct and Reversible Esterification of a Phosphonic Acid under Ambient Conditions through a Dissociative Mechanism

Marc‐André Légaré, Yuxiang Wei, Christina K. McCabe
article en

Abstract

Abstract We report the synthesis of 1-dimethylaminonaphthyl-8-phosphonic acid, which, in contrast with typical phosphonic acids, undergoes spontaneous condensation with alcohols to give monoesters under ambient conditions. The selectivity and reversibility of the reaction suggest that it occurs through a dissociative mechanism, inaccessible to typical phosphonic acids.

Inorganic Chemistry
Université de Sherbrooke (CA), McGill University (CA)
Openalex Percentile: Top 22%
Organophosphorus compounds synthesis
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