
Acta Cryst. (2011). C67, o85-o88 [ doi:10.1107/S0108270111002836 ]
Abstract: The structures of new oxaindane spiropyrans derived from 7-hydroxy-3',3'-dimethyl-3'H-spiro[chromene-2,1'-isobenzofuran]-8-carbaldehyde (SP1), namely N-benzyl-2-[(7-hydroxy-3',3'-dimethyl-3'H-spiro[chromene-2,1'-isobenzofuran]-8-yl)methylidene]hydrazinecarbothioamide, C27H25N3O3S, (I), at 120 (2) K, and N'-[(7-hydroxy-3',3'-dimethyl-3'H-spiro[chromene-2,1'-isobenzofuran]-8-yl)methylidene]-4-methylbenzohydrazide acetone monosolvate, C27H24N2O4·C3H6O, (II), at 100 (2) K, are reported. The photochromically active Cspiro-O bond length in (I) is close to that in the parent compound (SP1), and in (II) it is shorter. In (I), centrosymmetric pairs of molecules are bound by two equivalent N-H
S hydrogen bonds, forming an eight-membered ring with two donors and two acceptors.
Formula: C27H25N3O3S and C27H24N2O4·C3H6O
![]() ![]() Structure factor file (CIF format) (202.8 kbytes) | |
![]() ![]() Structure factor file (CIF format) (223.8 kbytes) | |
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