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3,6-Dihydroxy-2′-[(2-hydroxy-1-naphthyl)methyleneamino]xanthene-9-spiro-1′-isoindolin-3′-one acetonitrile solvate
The title compound, C(31)H(20)N(2)O(5)·C(2)H(3)N, was synthesized by the reaction of fluorescein hydrazide and excess 2-hydroxy-1-naphthaldehyde in acetonitrile. The spirolactam ring is planar and is nearly at right angles to the two benzene rings of the xanthene system. The dihedral angle between...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960338/ https://www.ncbi.nlm.nih.gov/pubmed/21201469 http://dx.doi.org/10.1107/S1600536808000974 |
Sumario: | The title compound, C(31)H(20)N(2)O(5)·C(2)H(3)N, was synthesized by the reaction of fluorescein hydrazide and excess 2-hydroxy-1-naphthaldehyde in acetonitrile. The spirolactam ring is planar and is nearly at right angles to the two benzene rings of the xanthene system. The dihedral angle between the two benzene rings of the xanthene system is 9.92 (4)°. In the crystal structure, the molecules are linked into extended two-dimensional networks by intermolecular hydrogen bonding. Acetonitrile molecules are located in the voids between the two-dimensional networks. |
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