Priscila S. V. Lima, Gustavo H. Weimer, Leonardo P. Oliveira, Helivaldo D. S. Souza, Gabriela F. Fiss, Helio G. Bonacorso and Marcos A. P. Martins
CrystEngComm, 2023,25, 4976-4991
Abstract
The quest for understanding crystal structures using supramolecular cluster demarcation has been applied to various uncharged compounds, and, more recently, to charged compounds. So, what would be the supramolecular behavior of mesoionic compounds?
Jessica M. L. Rosa, Priscila S. V. Lima, Helio G. Bonacorso, Nilo Zanatta and Marcos A. P. Martins
CrystEngComm, 2024,26, 796-808
Abstract
The supramolecular organization of organic salts has been widely researched, revealing recurring patterns in crystalline lattices that describe their supramolecular properties.
Anderson B. Pagliari, Jéssica M. L. Rosa, Priscila S. V. de Lima, Geórgia C. Zimmer, Maria E. C. da Silva, Érica G. de Oliveira, Helio G. Bonacorso, Nilo Zanatta and Marcos A. P. Martins
CrystEngComm, 2023,25, 5118-5132
Abstract
Variations in solvents, flexibility, and the presence/absence of amide–amide interactions can modulate the competition between amide-containing isoxazole polymorphs.
Anderson B. Pagliari, Alexandre R. Meyer, Vanessa B. Solner, Jéssica M. L. Rosa, Manfredo Hörner, Helio G. Bonacorso, Nilo Zanatta and Marcos A. P. Martins
CrystEngComm, 2022,24, 5348-5363
From themed collection:
CrystEngComm up-and-coming articles
Abstract
Crystallization mechanisms were proposed to investigate hydrogen bond and aromatic donor–acceptor interactions in a series of phenyl–perfluorophenyl amides. The modulation of NH⋯O![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif)
C bonds and aryl complementarity drove a new cocrystal growth.
Patrick Teixeira Campos, Gabriel Machado Rodrigues, Luiza Pereira Afonso, Vanessa Uecker Krüger, Rubia Mara Siqueira da Silva and Marcéo Auler Milani
CrystEngComm, 2022,24, 2667-2678
Abstract
The current investigation provides energetic and contact surface data on intermolecular interactions, correlates theoretical data with experimental data and suggests a proposal for nucleation for halogenated aryl amides.