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Optically active dendrimers, containing a planar chiral [2.2]paracyclophane as the X ‐ shaped core unit, were synthesized. Gram ‐ scale optical resolution and transformations of 4,7,12,15 ‐ tetrasubstituted [2.2]paracyclophanes were also carried out. The high ‐ generation dendrons effectively absorbed UV light and transferred the energy to the core, resulting in high photoluminescence from the core. In addition, the dendrons sufficiently isolated the emissive X ‐ shaped core, and intense circularly polarized luminescence was observed from thin dendrimer films. More information can be found in the Full Paper by Y. Morisaki, Y. Chujo et al. on page 2291 ff. [ABSTRACT FROM AUTHOR]

Planar chiral 4,7,12,15 ‐ tetrasubstituted [2.2]paracyclophane scaffolds stacked two AIE ‐ active monomers in close proximity at a chiral position. The resulting dimer exhibited strong emission even in a diluted solution by the suppression of the molecular motion. In particular, this binding effect could be readily released by heating. As a result, drastic changes in luminescent behavior were observed around room temperature regions. The dimers also showed excellent circular dichroism (CD) and circularly polarized luminescence (CPL) profiles. More information can be found in the Full Paper by M. Gon, Y. Morisaki and Y. Chujo on page 6323 ff. [ABSTRACT FROM AUTHOR]

Optically active, Fréchet-type dendrimers containing an emissive X-shaped π-electron system as the core unit were synthesized. Gram-scale optical resolution and transformations of 4,7,12,15-tetrasubstituted [2.2]paracyclophanes were also carried out. The high-generation dendrons effectively absorbed UV light and transferred energy to the core, resulting in high photoluminescence (PL) from the core. In addition, the dendrons sufficiently isolated the emissive X-shaped conjugated core and bright emission was observed from both thin films and solutions. Intense circularly polarized luminescence (CPL) was observed from the thin film. The dendrimer films exhibited excellent optical properties, such as large molar extinction coefficients, high fluorescence quantum efficiencies, intense PL and CPL, and large CPL dissymmetry factors. [ABSTRACT FROM AUTHOR]

Herein, we report a simple one-pot route to enantiopure copper(I) complexes featuring a unique [2.2]paracyclophane-based P,N-ligand system. Phosphine and pyridine moieties can be varied allowing the modular synthesis of these rigid and stable [2.2]paracyclophane-based P,N-ligands. These P,N-ligands are a new ligand class for different transition-metal complexes, which is shown exemplarily for palladium(II). [ABSTRACT FROM AUTHOR]