A beta-diketone dye was packed into the two-dimensional nanospace of a synthetic smectite (Sumecton SA), which is a cation-exchangeable layered silicate, to induce strong emission owing to molecular packing of the dye. An emissive dye, 1-(4-methoxyphenyl)-3-(4-pyridyl)-1,3-propandione, was prepared through a Claisen condensation reaction; the dye exhibited aggregation-induced emission, which is enhanced emission owing to clustering of molecules to form aggregates in poor solvents or in the solid state. The dye was nonemissive in solution. However, strong green emission was observed because of the restriction of molecular motion when the protonated dye was accommodated into the interlayer nanospace of the silicate layers through cation-exchange reactions. The restricted motion was confirmed by the smaller nonradiative relaxation rate constant obtained by time-resolved luminescence and quantum yield measurements. A moderate dye packing (0.11 mmol/g) in the interlayer space is important to obtain enhanced emission, whereas the intercalation of a large amount of dye (0.27 mmol/g) resulted in concentration quenching. Therefore, the interlayer space of the layered silicate used here was responsible for the strong emission because of moderate packing of the accommodated beta-diketones.