Volume 58, Issue 11 pp. o1315-o1317

Salicyl­aldoximium 3,5-di­nitro­salicyl­ate dihydrate

First published: 29 July 2004
Graham Smith, e-mail: [email protected]

Abstract

The crystal structure of the dihydrate of the 1:1 proton-transfer compound of 3,5-di­nitro­salicylic acid with 2-hydroxy­benz­aldehyde oxime (salicyl­aldoxime), C7H8NO2+·C7H3­N2O7·2H2O, is a three-dimensional hydrogen-bonded polymer. In this, the oxime-N atom of salicyl­aldoxime is protonated and, together with the adjacent O—H group, gives primary cyclic asymmetric hydrogen-bonding associations with both carboxyl O atoms of the acid. These, together with hydrogen-bonding interactions among all species present, including the two water mol­ecules, give an essentially planar ten-membered ring. Peripheral hydrogen bonding also links the water mol­ecules to carboxyl and nitro-O atoms, giving rise to a three-dimensional polymer structure.

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