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[Hydroxy(aryl)methylene]diphos­phonic acids,a class of drugs in bone pathology treatments,crystallize as head‐to‐head dimers
Authors:Marc Lecouvey  Carole Barbey  Alda Navaza  Alain Neuman  Thierry Prang
Institution:Marc Lecouvey,Carole Barbey,Alda Navaza,Alain Neuman,Thierry Prangé
Abstract:Two hydroxy­(aryl)­methyl­ene]­di­phospho­nic acids have been crystallized as dimers. The first compound, hydroxy­(phenyl)­methyl­ene]­di­phospho­nic acid monohydrate, C7H10O7P2·H2O, crystallizes in the non‐centrosymmetric space group P21, with the two enantiomers related by a non‐crystallographic centre of inversion, while the second compound, hydroxy(4‐nitro­phenyl)­methyl­ene]­di­phospho­nic acid tetra­hydro­furan disolvate, C7H9NO9P2·2C4H8O, crystallizes in the centrosymmetric space group P21/c and uses the centre of symmetry to form the same dimer.
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