[:pb]Different classical hydrogen-bonding patterns in three salicylaldoxime derivatives, 2-HO-4- C H C=NOH ( = Me, OH and MeO)[:]

[:pb]Authors: Gomes, L. R.; De Souza, M. V. N.; Da Costa, C. F.; Wardell, J. L.; Low, J. N.
Source: Acta Crystallographica Section e, Crystallographic Communications, v. 74, p. 1480-1485, 2018
Publisher: Science Direct

Abstract

The crystal structures of three salicyaldoxime compounds, namely 2-hy­droxy-4-methyl­benzaldehyde oxime, C₈H₉NO₂, 1, 2,4-di­hydroxy­benzaldehyde oxime, C₇H₇NO₃, 2, and 2-hy­droxy-4-meth­oxy­benzaldehyde oxime, C₈H₉NO₃, 3, are discussed. In each compound, the hydroxyl groups are essentially coplanar with their attached phenyl group. The inter­planar angles between the C=N—O moieties of the oxime unit and their attached phenyl rings are 0.08 (9), 1.08 (15) and 6.65 (15)° in 1, 2 and 3, respectively. In all three mol­ecules, the 2-hy­droxy group forms an intra­molecular O—HN(oxime) hydrogen bond. In compound (1), inter­molecular O—H(oxime)O(hydrox­yl) hydrogen bonds generate R²₂(14) dimers, related by inversion centres. In compound 2, inter­molecular O—H(oxime)O(4-hy­droxy) hydrogen bonds generate C9 chains along the b-axis direction, while O—H(4-hydrox­yl)O(2-hydrox­yl) inter­actions form zigzag C6 spiral chains along the c-axis direction, generated by a screw axis at 1, y, 1/4: the combination of the two chains provides a bimolecular sheet running parallel to the b axis, which lies between 0–1/2 c and 1/2–1 c. In compound 3, similar C9 chains, along the b-axis direction are generated by O—H(oxime)O(4-meth­oxy) hydrogen bonds. Further weaker, C—Hπ (in 1), π–π (in 2) and both C—Hπ and π–π inter­actions (in 3) further cement the three-dimensional structures. Hirshfeld surface and fingerprint analyses are discussed.

Keywords: crystal structure; hydrogen bonding; salicylaldoxime; Hirshfeld surface analysis

Document Type: Research Article

DOI: 10.1107/S2056989018013361

Publication date: 2018

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