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Mechanochemically Assisted Synthesis of Hexaazatriphenylenehexacarbonitrile

[Image: see text] 1,4,5,8,9,11-hexaazatriphenylenehexacarbonitrile (HAT CN) was synthesized mechanochemically at room temperature. The coupling of hexaketocyclohexane and diaminomaleonitrile was conducted in 10 min by vibratory ball milling. The effects of milling parameters, acids, dehydrating agen...

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Detalles Bibliográficos
Autores principales: Pickhardt, Wilm, Wohlgemuth, Maximilian, Grätz, Sven, Borchardt, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524413/
https://www.ncbi.nlm.nih.gov/pubmed/34014673
http://dx.doi.org/10.1021/acs.joc.1c00253
Descripción
Sumario:[Image: see text] 1,4,5,8,9,11-hexaazatriphenylenehexacarbonitrile (HAT CN) was synthesized mechanochemically at room temperature. The coupling of hexaketocyclohexane and diaminomaleonitrile was conducted in 10 min by vibratory ball milling. The effects of milling parameters, acids, dehydrating agents, and liquid-assisted grinding were rationalized. With 67%, the yield of this mechanochemical approach exceeds that of state-of-the-art wet-chemical syntheses while being superior with respect to time-, resource-, and energy-efficiency as quantified via green metrics.