Ultralarge Stokes Shift Phosphorescence Artificial Harvesting Supramolecular System with Near‐Infrared Emission

A two‐step sequential phosphorescence harvesting system with ultralarge Stokes shift and near‐infrared (NIR) emission at 825 nm is successfully constructed by racemic 1,2‐diaminocyclohexan‐derived 6‐bromoisoquinoline (BQ), cucurbit[8]uril (CB[8]), and amphipathic sulfonatocalix[4]arene (SC4AD) via cascaded assembly strategy in aqueous solution. In virtue of the confinement effect of CB[8] with rigid cavity, BQ can generate an emerging phosphorescent emission at 555 nm. Subsequently, the binary BQ⊂CB[8] further assemblies with SC4AD to form close‐packed spherical aggregate, which contributes to the dramatic enhancement of phosphorescence emission intensity ≈30 times with prolonged lifetime from 21.3 µs to 0.364 ms. Notably, the BQ⊂CB[8]@SC4AD assembly can serve as an energy donor to conduct stepwise phosphorescence harvesting process through successive introduction of primary acceptors, cyanine 5 (Cy5) or nile blue (NiB), and secondary acceptor, heptamethine cyanine (IR780). The final aggregate with remarkable ultralarge Stokes shift (≈525 nm) and long‐lived NIR photoluminescence (PL) emission at 825 nm is further employed as imaging agent for NIR cell labeling. A stepwise phosphorescence artificial harvesting supramolecular system is constructed using 1,2‐diaminocyclohexan‐derived 6‐bromoisoquinoline, cucurbit[8]uril, and amphipathic sulfonatocalix[4]arene in aqueous solution through successively introducing primary acceptors (Cy5 or NiB) and final acceptor (IR780), presenting ultralarge Stokes shift (≈525 nm) and long‐lived NIR photoluminescence emission at 825 nm, thus being successfully applied for NIR cell labeling.