Success or Failure of Chiral Crystallization of Similar Heterocyclic Compounds

Single crystals of two achiral and planar heterocyclic compounds, C(9)H(8)H(3)O(CA1) and C(8)H(5)NO(2) (CA4), recrystallized from ethanol, were characterized by single crystal X-ray analysis, respectively, and chiral crystallization was observed only for CA1 as P2(1)2(1)2(1) (# 19), whereas it was n...

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Detalles Bibliográficos
Autores principales: Chunkang, Cyprian M., Ikome, Iris E., Nfor, Emmanuel N., Mitani, Yuta, Katsuumi, Natsuki, Haraguchi, Tomoyuki, Akitsu, Takashiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731153/
https://www.ncbi.nlm.nih.gov/pubmed/33276663
http://dx.doi.org/10.3390/molecules25235691
Descripción
Sumario:Single crystals of two achiral and planar heterocyclic compounds, C(9)H(8)H(3)O(CA1) and C(8)H(5)NO(2) (CA4), recrystallized from ethanol, were characterized by single crystal X-ray analysis, respectively, and chiral crystallization was observed only for CA1 as P2(1)2(1)2(1) (# 19), whereas it was not observed for CA4 P2(1)/c (# 14). In CA1, as a monohydrate, the hydrogen bonds were pronounced around the water of crystallization (O4), and the planar cyclic sites were arranged in parallel to slightly tilted positions. On the other hand, an anhydride CA4 formed a dimer by hydrogen bonds between adjacent molecules in the crystal, which were aggregated by van der Waals forces and placed in parallel planar cyclic sites.

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