Incorporation of fluorine atoms into the tolane backbone constructed tight crystal packing structures to suppress molecular motions, which provided dramatic enhancement of photoluminescence efficiency in crystalline state.
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Halogen bond interactions, which take place between an electrophilic halogen and the electron-pair of a Lewis base and exhibit high directionality (approximately 180°), are non-covalent bond interactions similar to the hydrogen bond interaction. Many reports on halogen bond interactions have been published thus far, but many of them discuss halogen bond in the context of crystal engineering or supramolecular architecture. Since a seminal report by Bolm in 2008, halogen bond-assisted or -promoted organic synthesis has received significant attention. This review aims to introduce the molecular design of suitable halogen bond donors and organic transformations involving halogen bond interactions to afford a variety of organic compounds.
Light-emitting liquid-crystalline polymers showing PL in the pristine solid state can control their PL color from blue to light-blue via a thermal phase transition to LC phases, which originates from a dynamic change of aggregated structures.
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