Supramolecular architectures of conformationally controlled 1,3-phenyl-dioxalamic molecular clefts through hydrogen bonding and steric restraints

In this contribution the supramolecular architecture of a series of six 1,3-phenyl-dioxalamic molecular clefts is described. The conformation was controlled by the use of Me and OMe group substitution in the phenyl spacer. The structural and conformational study was carried out by X-ray diffraction...

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Veröffentlicht in:CrystEngComm 2011-01, Vol.13 (14), p.4748-4761
Hauptverfasser: González-González, Juan Saulo, Martínez-Martínez, Francisco Javier, Peraza Campos, Ana Lilia, de Jesus Rosales-Hoz, Maria, García-Báez, Efrén V., Padilla-Martínez, Itzia I.
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Sprache:eng
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