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Tautomeric properties, conformations and structure of N-(2-hydroxyphenyl)-4-amino-3-penten-2-on
Authors:M Kabak  A Elmali  Y Elerman
Institution:Department of Engineering Physics, Faculty of Sciences, University of Ankara, 06100 Be?evler, Ankara, Turkey
Abstract:N-(2-hydroxyphenyl)-4-amino-3-penten-2-on (C11H13NO2) has been studied by X-ray analysis. It crystallizes the orthorhombic space group P212121 with a=8.834(1), b=10.508(2), c=11.212(2) Å, V=1040.8(3) Å3, Z=4, Dc=1.22 g cm−3 and μ(MoKgreek small letter alpha)=0.084 mm−1. The structure was solved by direct methods and refined to R=0.038 for 1373 reflections (I>2σ(I)). The title compound is photochromic and the molecule is not planar. Intramolecular hydrogen bonds occur between the pairs of atoms N(1) and O(1) 2.631(2) Å], and N(1) and O(2) 2.641(2) Å], the H atom essentially being bonded to the N atom. There is also a strong intermolecular O–Hcdots, three dots, centeredO hydrogen bonding 2.647(2) Å] between neighbouring molecules. Tautomeric properties and conformations of the title compound were investigated by semi-empirical quantum mechanical AM1 calculations and the results are compared with the X-ray results.
Keywords:X-ray  Schiff base  AM1  Photochromic  Tautomerism
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