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Comprehensive Summary Polycatenane gels have attracted extensive attention due to their high degree of freedom and mobility. However, the syntheses of poly[2]catenane gels reported to date all rely on the polymer as the backbone. Herein, we prepared poly[2]catenane gels based on entirely sequential assembly of small molecules. Monomer M1 with two unclosed rings was first prepared, which self‐assembled to form supramolecular polymers (SPs) via hydrogen bonding and π‐π interactions. Upon adding small molecule monomers M2 and M3 with aldehyde groups, ring closing of SPs occurred because the amino groups in the SPs reacted with M2 to form imine bonds. In addition, M3, which had twice the number of aldehyde groups as M2, enabled SPs to ring‐close, causing the proceeding of crosslinking process at the same time. Thus linear SPs were transformed into poly[2]catenane gel networks. Due to the presence of hydrogen bonds in the poly[2]catenane gel, the gel also possessed stimulus responsiveness and self‐healing properties. [ABSTRACT FROM AUTHOR]

Traditional multicolor fluorescent hydrogels are generated through the assembly of discrete fluorescent hydrogels, which is not a complete integration much distinct from living organisms. On the basis of aggregation‐induced emission (AIE), a special solvent polar‐responsive AIE molecule possessing a twisted intramolecular charge transfer (TICT) effect was noticed. By incorporating it into the gel network, an AIE gel that displays continuous gradient fluorescence was fabricated. First, hydrogel A containing the solvent polar‐responsive AIE‐gen was prepared to show orange fluorescence. After soaking in the organic solvents, the fluorescence color transition of hydrogel A ranging from orange to green occurred when being immersed in high‐polarity organic solvents ascribed to the embedded AIE‐gen owning TICT effect. Then, hydrogel A was successively lifted up from organic solvents. Due to the different immersion time of each section for the hydrogel, the polarity difference occurred. Then, the produced gel B showed continuous gradient fluorescence ranging from orange to green under the irradiation of UV light. [ABSTRACT FROM AUTHOR]

A probe, MITO-TPE, was developed for imaging mitochondrial SO2 with good selectivity, high sensitivity, and a fast response time. Cell imaging indicated that SO2-induced oxidative stress may cause damage to cells through O2˙− bursting. MITO-TPE has here been used to image the misregulation of SO2 levels in mitochondria during heat stroke for the first time. [ABSTRACT FROM AUTHOR]

A probe, MITO-TPE, was developed for imaging mitochondrial SO 2 with good selectivity, high sensitivity, and a fast response time. Cell imaging indicated that SO 2 -induced oxidative stress may cause damage to cells through O 2 ˙ - bursting. MITO-TPE has here been used to image the misregulation of SO 2 levels in mitochondria during heat stroke for the first time.