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Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π--π stacking.
Yelgaonkar, Shweta P; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Afiliación
  • Yelgaonkar SP; Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA. len-macgillivray@uiowa.edu.
  • Kiani D; Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, Pennsylvania 18015, USA.
  • Baltrusaitis J; Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, Pennsylvania 18015, USA.
  • MacGillivray LR; Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA. len-macgillivray@uiowa.edu.
Chem Commun (Camb) ; 56(49): 6708-6710, 2020 Jun 18.
Article en En | MEDLINE | ID: mdl-32420555
ABSTRACT
Salt cocrystals with components that assemble by hydrogen bonds and aromatic anion-molecule stacks (π--π stacks) are reported. U-shaped bipyridines and an isocoumarin carboxylic acid self-assemble to form 5-, 6-, and 10-component aggregates with components in double and quadruple face-to-face stacks. DFT calculations support the π--π stacks to help stabilize the salt cocrystals.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article