A co-crystal strategy for the solidification of liquid pyrazine derivatives: X-ray structures and Hirshfeld surface analyses
Autor: | Cui-Min Yan, Ya-an Zhang, Chen Chen, Xiao-Qing Zhao, Bai-Wang Sun, Abul Monsur Showkot Hossain |
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Rok vydání: | 2020 |
Předmět: |
Diffraction
Pyrazine 010405 organic chemistry Hydrogen bond Organic Chemistry Intermolecular force Supramolecular chemistry Stacking 010402 general chemistry 01 natural sciences 0104 chemical sciences Analytical Chemistry Inorganic Chemistry Crystal Crystallography chemistry.chemical_compound chemistry Melting point Spectroscopy |
Zdroj: | Journal of Molecular Structure. 1218:128505 |
ISSN: | 0022-2860 |
DOI: | 10.1016/j.molstruc.2020.128505 |
Popis: | Here we described a co-crystal strategy for the solidification of liquid 2,3-dimethylpyrazine (2,3-DMP), 2,5-dimethylpyrazine (2,5-DMP), 2,6-dimethylpyrazine (2,6-DMP) with the poly-substituted salicylic acids [3,5,6-trichlorosalicylic acid (TCSA) and 3,5-dinitrosalicylic acid (DNSA)] under identical conditions. Those newly grown co-crystals (2,3-DMP:TCSA = 1:1 for 1; 2,5-DMP:TCSA = 1:2 for 2; 2,6-DMP:DNSA = 1:1 for 3) were characterized by single-crystal X-ray diffraction. The structure determination shows that strong O-H⋯N hydrogen bonds play an important role in connection of pyrazine derivatives and poly-substituted salicylic acids. Moreover, aromatic cycle stacking interactions play a crucial role in the 3D supramolecular network. Hirshfeld surfaces and fingerprint plots of the reported co-crystals were analyzed, which showed that O-H⋯N, C-H⋯O, H⋯H, H⋯Cl and aromatic cycle stacking intermolecular interactions are the main stabilizing factors of the co-crystal structures. The melting points studies showed that the co-crystal strategy is effective for solidification of liquid pyrazine derivatives. |
Databáze: | OpenAIRE |
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