Carbonyl–carbonyl, carbonyl–π and carbonyl–halogen dipolar interactions as the directing motifs of the supramolecular structure of ethyl 6-chloro-2-oxo-2H-chromene-3-carboxylate and ethyl 6-bromo-2-oxo-2H-chromene-3-carboxylate
Copyright policy )Carbonyl–carbonyl, carbonyl–π and carbonyl–halogen dipolar interactions as the directing motifs of the supramolecular structure of ethyl 6-chloro-2-oxo-2H-chromene-3-carboxylate and ethyl 6-bromo-2-oxo-2H-chromene-3-carboxylate
The title compounds, C(12)H(9)ClO(4), (I), and C(12)H(9)BrO(4), (II), are isomorphous and crystallize in the monoclinic space group P2(1)/c. Both compounds present an anti conformation between the 3-carboxy and the lactone carbonyl groups. Both carbonyl groups are out of the plane defined by the remaining chromene atoms, by 8.37 (6) and 17.57 (6) degrees for (I), and by 9.07 (8) and 18.96 (18) degrees for (II), owing to their involvement in intermolecular interactions. In both compounds, layers of centrosymmetric hydrogen-bonded dimers are developed in the [-5 -2 22] plane through C-H...O interactions, involving both carbonyl groups as acceptors. Two families of dimers stack through C=O...C=O, C=O...pi and C-X...C=O (X = Cl and Br) dipolar interactions, as well as a C-H...pi interaction, developing the three-dimensional structure along the c axis.
- Universidad Autónoma del Estado de Morelos Mexico
- University of Colima Mexico
- Instituto Politécnico Nacional Mexico
Coumarins, Hydrocarbons, Chlorinated, Heterocyclic Compounds, 2-Ring, Hydrocarbons, Brominated
Coumarins, Hydrocarbons, Chlorinated, Heterocyclic Compounds, 2-Ring, Hydrocarbons, Brominated
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