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Journal of Structural Chemistry

2011 year, number 4

CRYSTAL STRUCTURES OF NEW 4-HYDROXY-N′-(3,5-DIIODO-2-HYDROXYBENZYLIDENE)BENZOHYDRAZIDE METHANOL AND 4-HYDROXY-N′-(2-METHOXYNAPHTH-1-YL-METHYLENE)BENZOHYDRAZIDE DIMETHANOL SOLVATE

Y.-J. Wei, F.-W. Wang
Department of Chemistry, Huainan Normal College
huainanweiyijun@163.com
Keywords: hydrazone, crystal structure, hydrogen bonding
Pages: 776-780

Abstract

Two new hydrazone compounds C14H10I2N2O3·CH3OH (1) and C19H16N2O3·2CH3OH (2) are synthesized by the condensation reactions of the equimolar quantities of 4-hydroxybenzohydrazide with 3,5-diiodo-2-hydroxybenzaldehyde and 2-methoxynaphth-1-yl-methylene respectively in methanol solutions. Compound 1 consists of a hydrazone molecule and a methanol molecule of crystallization, and compound 2 consists of a hydrazone molecule and two methanol molecules of crystallization. Both compounds are characterized by elemental analysis, IR spectra, and single crystal X-ray diffraction. As expected, each hydrazone molecule adopts an E configuration about the C=N double bond. In the crystal structures of both compounds, the hydrazone and methanol molecules are linked through intermolecular N-H⋯O and O-H⋯O hydrogen bonds, forming layers along the bc direction.