RESUMO
In recent years, host-guest interactions of macrocycles have attracted much attention as an emerging method for enhancing the intersystem crossing of pure organic room-temperature phosphorescence. In this work, we utilize cucurbit[8]uril (Q[8]) to specifically recognize synthetic bromophenyl pyridine derivatives (BPCOOH) to construct a highly stable charge-transfer dimer, where the bromophenyl pyridine moiety of BPCOOH is encapsulated by Q[8] in a 1:2 host/guest ratio. The assemblies exhibit specific recognition and detection properties for dodine on both fluorescence and phosphorescence spectra. Subsequently, the solid films were prepared by introducing carboxymethylcellulose sodium into the assemblies, which greatly enhanced its RTP performance by increasing the noncovalent bonding interactions, enabling the visualization of high-strength RTP and quantitative testing of the solid state. Finally, this material was used for the application of portable indicator papers to achieve rapid and visualized detection of dodine in daily life, which provides more possibilities for the potential applications of cucurbit[n]uril-based room-temperature phosphorescence material.
RESUMO
Three different complexes, TMeQ[6]-TBT, Q[7]-TBT, and Q[8]-TBT are constructed by three different cucurbiturils and synthesized by guest melamine-cored Schiff bases (TBT) through outer-surface interaction and host-guest interactions. TBT forms a TMeQ[6]-TBT complex with TMeQ[6] through outer-surface interaction, while Q[7]-TBT and Q[8]-TBT form complexes with Q[7,8] through host-guest interactions. Among them, Q[7]-TBT is selected as a UV detector for the detection of silver ions (Ag+). This work makes full use of the characteristics of each cucurbituril and melamine-cored Schiff base to construct a series of complexes and these are applied to metal detection.
