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   <subfield code="a">Solvent-induced Polymorphism of 2-[(2-Amino-phenylimino)-phenyl-methyl]-phenol</subfield>
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   <subfield code="a">The title compound C19H16N2O crystallize as either triclinic or monoclinic polymorph depending on the solvent used. Polymorph [1] crystallizes from methanol in the space group P $$ \mathop 1\limits^ - $$ with unit cell dimensions: a=8.723(2), b=9.344(2), c=10.544(2)Å, α=71.54(2), ß=78.74(2), γ=74.15(2)°, and Z=2. Polymorph [2] crystallizes from benzene with space group P21/n with unit cell dimensions: a=10.230(3), b=20.536(7), c=14.563(4) Å, ß=97.14(3)°, and Z=8. The only similarity between molecules of [1] and two independent molecules of [2] can be found in almost co-planar phenyl moiety with chelate ring. Both structures are characterized with strong intramolecular O-H···N hydrogen bond. Whereas the molecular interconnections in [2] are based on van der Waals attractions between discrete molecules, molecules of [1] associate in dimers via intermolecular N-H···O hydrogen bonding by the operation of crystallographic centre of inversion.</subfield>
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