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Bis{4-[(3-phenylallylidene)amino]cyclohexyl}methane trichloromethane solvate
The title compound, C(31)H(38)N(2), was prepared from bis(4-aminocyclohexyl)methane and two equivalents of cinnamaldehyde. The cyclohexyl groups each show a chair conformation and the α,β-unsaturated imine side chains are all-trans configured. Two molecules of the title compound as well as two...
| 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/PMC2959948/ https://www.ncbi.nlm.nih.gov/pubmed/21581335 http://dx.doi.org/10.1107/S1600536808037380 |
| Sumario: | The title compound, C(31)H(38)N(2), was prepared from bis(4-aminocyclohexyl)methane and two equivalents of cinnamaldehyde. The cyclohexyl groups each show a chair conformation and the α,β-unsaturated imine side chains are all-trans configured. Two molecules of the title compound as well as two trichloromethane solvent molecules are present in the asymmetric unit. The solvent molecules interact with the diimines via weak C—H⋯N hydrogen bonds. |
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