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Crystal and molecular structure of an enantiomeric gossypol-acetic acid clathrate
Authors:Michael K Dowd  Leonard M Thomas  Millard C Calhoun
Affiliation:(1) Department of Chemistry, Iowa State University, 50011 Ames, Iowa;(2) Texas Agricultural Experiment Station, 76901 San Angelo, Texas;(3) Southern Regional Research Center, ARS, USDA, 1100 Robert E. Lee Blvd., 70124 New Orleans, LA;(4) School of Biological Sciences, 007 Biological Sciences Bldg., 5100 Rockhill Rd., 64110 Kansas City, MO
Abstract:Single crystals of gossypol with three molecules of acetic acid (gossypol triacetic acid) were grown from solutions of gossypol acetic acid and acetone. The crystals were unstable in air but could be stabilized for X-ray diffraction analysis by coating the crystal surfaces with a thin layer of mineral oil. The gossypol triacetic acid complex (C30H30O8·3C2H4O2) forms an orthorhombic crystal system with P212121 (Z=4) symmetry. Unit cell dimensions were a=9.0208(7) Å, b=17.4884(10) Å, and c=24.358(2), Å yielding a volume of 3842.7(5) Å3 and a density of 1.2077(2) g/cm3. As with all previously reported crystals of gossypol, the gossypol molecules were of the aldehyde tautomer, and the two planar naphthalene rings were approximately perpendicular. Acetic acid molecules were found to lie in channels within the gossypol matrix. Individual crystals contained only one gossypol enantiomer, but both enantiomers crystallized from solution. Although the crystal habit could not be used to distinguish between the gossypol enantiomers, a fragment of the crystal could be derivatized and analyzed by high-performance liquid chromatography for this purpose. The ability to grow large, nonracemic crystals leads to a simple procedure for separating small quantities of the individual gossypol enantiomers.
Keywords:Gossypol  gossypol acetic acid  gossypol enantiomers  inclusion compounds  isomers  isomer separation
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