1015 wileyonlinelibrary.com COMMUNICATION for all existing host matrices. Limited pore size is a problem for cyclodextrins, low solubility and dispersibility of guest emitters limits PMMA and hydroxyl-steroids, and aggregation of guest emitters over time is common. Here, we propose metal-organic frameworks (MOFs) as host materials to suppress nonradiative decay processes because of their rigid porous structure and pore structures that can trap and stabilize emitter molecules. MOFs are crystalline materials composed of metal ions and organic ligands and are attracting considerable interest because of their thermal and chemical stability and ability to encapsulate a wide variety of guest species in their cavities, including gases, [ 12-14 ] nanopar-ticles, [ 15-17 ] enzymes, [ 18,19 ] and organic molecules. [ 20-22 ] The individual pores of MOFs can isolate guest emitters and restrict molecular motion by their rigid frameworks. There are a few reports describing the suppression of molecular motion or concentration quenching in MOFs, such as the inhibition of cis-trans isomerization of stilbene, [ 23 ] amplifi cation of fl uores-cence quantum yield, [ 24 ] and demonstration of a two-photon pumped laser. [ 25 ] However, these are not realizing long-lived organic triplet excitons and related phosphorescence of guest molecules. Although a number of phosphorescent MOFs are known, most of these emit only at low temperatures (77 K), indicating that nonradiative deactivation is dominant at room temperature. [ 26,27 ] In contrast, in all of the MOFs that exhibit room-temperature phosphorescence, the well-known heavy-atom effect is used. Heavy atoms such as I, Br, Pb, and Ir [ 28-34 ] incorporated in the structure of the framework itself or encapsulated within the pores enhance the rate of radiative decay from the triplet state k phos , rather than reducing the rate of nonradiative deactivation k nr. As a result, the phosphorescence lifetime of these MOFs is quite short (10 −3-10 −6 s), signifi cantly less than the lifetime desired for many applications. Moreover, since the origin of the photoluminescence is not a pure guest emitter but a metal-coordinated ligand or an exciplex between ligand and guest molecule, careful design of both the linker and MOF is necessary to achieve effi cient room-temperature phosphorescence. In this work, we demonstrate that long-lived emission from triplet excitons can be achieved even at high temperature by encapsulating organic emitter in MOFs. In addition , we show that thermally activated delayed fl uorescence (TADF) [ 35 ] can be achieved from MOF-encapsulated emitters at temperatures >300 K. TADF is an effi cient process to harvest triplet excitons for light emission especially in OLEDs; however, it requires careful molecular design of the emitter to enable thermal up-conversion from triplet exciton to singlet exciton. Our method realizes TADF from common aromatic molecules without any chemical modifi cation. As a proof of concept we used the well-known long-lived phosphorescent An abili...