The construction and precise control of the face-to-face π-stacked arrangements of anthracene fluorophores in the crystalline state led to a remarkable red shift in the fluorescence spectrum due to unprecedented excited oligomer formation. The arrangements were regulated by using organic salts including anthracene-1,5-disulfonic acid (1,5-ADS) and a variety of aliphatic amines. Because of the smaller number of hydrogen atoms at the edge positions and the steric effect of the sulfonate groups, 1,5-ADS should prefer face-to-face π-stacked arrangements over the usual edge-to-face herringbone arrangement. Indeed, as the alkyl substituents were lengthened, the organic salts altered their anthracene arrangement to give two-dimensional (2D) edge-to-face and end-to-face herringbone arrangements, one-dimensional (1D) face-to-face zigzag and slipped stacking arrangements, a lateral 1D face-to-face arrangement like part of a brick wall, and a discrete monomer arrangement. The monomer arrangement behaved as a dilute solution even in the close-packed solid state to emit deep blue light. The 1D face-to-face zigzag and slipped stacking of the anthracene fluorophores caused a red shift of 30-40 nm in the fluorescence emission with respect to the discrete arrangement, probably owing to ground-state associations. On the other hand, the 2D end-to-face stacking induced a larger red shift of 60 nm, which is attributed to the excimer fluorescence. Surprisingly, the brick-like lateral face-to-face arrangement afforded a remarkable red shift of 150 nm to give yellow fluorescence. This anomalous red shift is probably due to excited oligomer formation in such a lateral 1D arrangement according to the long fluorescence lifetime and little shift in the excitation spectrum. The regulation of the π-stacked arrangement of anthracene fluorophores enabled the wide modulation of the fluorescence and a detailed investigation of the relationships between the photophysical properties and the arrangements.

Herein we report the first example of chiral recognition and kinetic resolution of aromatic amine guests using supramolecular nanocapsules assembled from cyclodextrin derivatives in nonpolar media. With these nanocapsules, an extremely high chiral recognition of 1-(1-naphthyl)ethylamine (1) in cyclohexane was achieved, with a binding selectivity of up to 41 for (S)-1 over (R)-1. In addition, kinetic resolution of 1 through enantioselective N-acylation was accomplished with an enantiomeric excess of up to 91%.

Luminescent jewels: Unusually shaped fluorescent supramolecular clusters assemble into one‐dimensional π‐stacked supramolecular beads to eventually crystallize with a wide range of solvent molecules (see picture). The included solvent molecules modulate the fluorescence colors of the inclusion crystals from blue to orange‐yellow as is known for the colors of gemstones.

Organic salts of anthracene-2,6-disulfonic acid (ADS) with a wide variety of primary amines have been fabricated, and their arrangements of anthracene molecules and solid-state fluorescence properties investigated. Single-crystal X-ray studies reveal that the salts show seven types of crystal forms and corresponding molecular arrangements of anthracene moieties depending on the amine, while anthracene shows only one form and arrangement in the solid state. Depending on the molecular arrangements, the ADS salts exhibit various solid-state fluorescence properties: spectral shift (30 nm) and suppression and enhancement of the fluorescence intensity. Especially the ADS salt with n-heptylamine (nHepA), which shows discrete anthracene moieties in the crystal, exhibits the highest quantum yield (Phi(F)=46.1+/-0.2%) in the series of ADS salts, which exceeds that of anthracene crystal (Phi(F)=42.9+/-0.2%). From these systematic investigations on the arrangements and the solid-state properties, the following factors are essential for high fluorescence quantum yield in the solid state: prevention of contact between pi planes of anthracene moieties and immobilization of anthracene rings. In addition, such organic salts have potential as a system for modulating the molecular arrangements of fluorophores and the concomitant solid-state properties. Thus, systematic investigation of this system constructs a library of arrangements and properties, and the library leads to remarkable strategies for the development of organic solid materials.

Voltammetric measurement was performed with a solid electrode surface which was renewed every several seconds by laser-ablation. The voltammograms obtained were, in appearance, quite similar to polarograms obtained with a dropping mercury electrode (DME). Oxidation waves of [Fe(CN)6]4− and l-ascorbic acid were examined by this voltammetry.