Hirshfeld Surface Analysis of Substituted Phenols

Adam Martin, Karel Hartlieb, Alexandre Sobolev, Colin Raston

    Research output: Contribution to journalArticlepeer-review

    48 Citations (Scopus)

    Abstract

    The effect of para-substituents on the crystal packing of phenols has been investigated, for systems bearing nonpolar groups (tert-butyl and benzyl, compounds 1 and 2, respectively) and for methylene linked bis-phenol bearing polar nitro groups (compound 3). Remarkable for 1 and 2, the asymmetric unit has six molecules, which form infinite helical hydrogen bonded arrays in the extended structures, whereas compound 3 bearing nitro groups coplanar with the phenol rings forms almost columnar arrays. Hirshfeld surface analysis is used to show that despite packing in a nearly identical manner, 1 and 2 are distinctly different in their interactions, and these structures are compared to compound 3, where the solid-state interactions are dominated by the nitro moieties.

    Original languageEnglish
    Pages (from-to)5302-5306
    Number of pages5
    JournalCrystal Growth and Design
    Volume10
    Issue number12
    DOIs
    Publication statusPublished - 1 Dec 2010

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