Molecular bricklaying: The protonated benzimidazole moiety as a synthon for crystal engineering

Craig J. Matthews, Vanessa Broughton, Gérald Bernardinelli, Xavier Melich, Guy Brand, Anthony C. Willis, Alan F. Williams*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    42 Citations (Scopus)

    Abstract

    The crystal structures of three salts of diprotonated 1,2-bis(1H-benzimidazol-2-yl)ethane, 1, with tetrahalogenometallates are reported. The crystal lattices are constructed from two types of interactions, the stacking of the protonated benzimidazole groups and N-H⋯Cl hydrogen bonding between the cations and the complex anions. Depending on the conformation of the cation, two- or three-dimensionally stacked structures are formed. A similar packing motif is found with the related cation formed by 1,3-bis(1H-benzimidazol-2-yl)-propane, 2, and this suggests that the protonated benzimidazole group may be a useful synthon for crystal engineering.

    Original languageEnglish
    Pages (from-to)354-358
    Number of pages5
    JournalNew Journal of Chemistry
    Volume27
    Issue number2
    DOIs
    Publication statusPublished - 1 Feb 2003

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