A. Mucha et al., RESOLUTION, CRYSTAL-STRUCTURE AND ABSOLUTE-CONFIGURATION OF THE ENANTIOMERS OF AMINOPHENYLMETHANEPHOSPHONOUS ACID HYDRATE, Phosphorus, sulfur and silicon and the related elements, 92(1-4), 1994, pp. 129-138
Enantiomers of aminophenylmethanephosphonous acid have been obtained b
y resolution of the racemic acid using optically active isomers of l-p
henylethylamine. The crystal and molecular structures of the enantiome
rs of the acid monohydrate (C7H10PO2N . H2O) have been determined by s
ingle-crystal X-ray diffraction method. The crystals are monclinic, of
space grup P2(1)2(1)2(1) and Z = 4. Cell constants: a = 5.410(2) Angs
trom, b = 6.603(2) Angstrom, c = 25.061(5) Angstrom for (+)-(R)-enanti
omer and a = 5.414(2) Angstrom, b = 6.602(2) Angstrom, c = 25.056(5) A
ngstrom for (-)-(S)-enantiomer. The structures solved by direct method
have been refined to final R = 0.033 and R = 0.029 respectively.