Supramolecular architecture based on [Fe(CN)6]3− metallotectons and melaminium synthons

Assembly involving [Fe(CN)6]3− metallotectons as building units and melaminium organic cation has been envisioned in order to elaborate a hybrid supramolecular based on ionic H-bonds with formula {(H-mel)4[Fe(CN)6]Cl} (H-mel+: melaminium cation). The compound has been prepared by diffusion method an...

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Veröffentlicht in:Journal of molecular structure 2017-10, Vol.1146, p.409-416
Hauptverfasser: Krichen, Firas, Walha, Siwar, Lhoste, Jérôme, Bulou, Alain, Kabadou, Ahlem, Goutenoire, François
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Sprache:eng
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Zusammenfassung:Assembly involving [Fe(CN)6]3− metallotectons as building units and melaminium organic cation has been envisioned in order to elaborate a hybrid supramolecular based on ionic H-bonds with formula {(H-mel)4[Fe(CN)6]Cl} (H-mel+: melaminium cation). The compound has been prepared by diffusion method and characterized by single-crystal X-ray diffraction, EDX analysis, and Raman-IR spectroscopies with assignment from ab initio calculations. The melaminium exhibit self cationic coupling with cyclic hydrogen bonds to give a one dimensional {[H-mel]+}∝ synthon. Therefore, these cationic ribbons are inter-linked via hydrogen bonds by the anionic tectons [Fe(CN)6]3− and chlorine anion resulting on a 3D network. Molecular hirshfeld surfaces revealed that the crystal structure has been supported mainly by NH⋯N and NH⋯Cl intermolecular Hydrogen bonds and by favoured C⋯C and C⋯N weak interactions. [Display omitted] •The (H-mel)4[Fe(CN)6]Cl compound was prepared by diffusion method and characterized by single crystal X-ray diffraction.•EDS and PXRD analysis, and Raman-IR spectroscopies with assignment from ab initio calculations were performed.•One dimensional {[H-mel]+}µ synthons are inter-linked via H-bonds by the anionic tectons [Fe(CN)6]3− and chlorine anions.•Intermolecular interactions were analyzed by hirshfeld surfaces and resulting enrichment ratio calculations.
ISSN:0022-2860
1872-8014
0022-2860
DOI:10.1016/j.molstruc.2017.05.123