Abstract:A methylene- and adamantane-bridged macrocycle with biphenyl units showed selective co-inclusion of n-hexane among the hexane isomers through crystallization. In the use of n-pentane or n-heptane, inclusion crystals with alkanes were not formed.
“…6a). 35 We found that macrocycle (4) had a nearly rhombic structure with a cavity, in which dichloromethanes as crystallization solvent were contained by means of C-H⋯π and C-H⋯O interactions between the hydrogen atoms of the dichloromethanes and the biphenyl units or the oxygen atoms of the methoxy groups. The use of dibromomethane instead of dichloromethane resulted in the formation of crystal 4a.…”
Inclusion crystals containing several halocarbons were formed by three types of diimide-based macrocycles. Iodomethane was encapsulated within the cavity of the macrocycle through halogen-related interactions.
“…6a). 35 We found that macrocycle (4) had a nearly rhombic structure with a cavity, in which dichloromethanes as crystallization solvent were contained by means of C-H⋯π and C-H⋯O interactions between the hydrogen atoms of the dichloromethanes and the biphenyl units or the oxygen atoms of the methoxy groups. The use of dibromomethane instead of dichloromethane resulted in the formation of crystal 4a.…”
Inclusion crystals containing several halocarbons were formed by three types of diimide-based macrocycles. Iodomethane was encapsulated within the cavity of the macrocycle through halogen-related interactions.
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