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Ultra‐low molecular weight (ULMW) CO2‐polyols with well‐defined hydroxyl end groups represent useful soft segments for the preparation of high‐performance polyurethane foams. However, owing to the poor proton tolerance of catalysts towards CO2/epoxide telomerization, it remains challenging to synthesize ULMW yet colorless CO2‐polyols. Herein, we propose an immobilization strategy of constructing supported catalysts by chemical anchoring of aluminum porphyrin on Merrifield resin. The resulting supported catalyst displays both extremely high proton tolerance (≈8000 times the equivalents of metal centers) and independence of cocatalyst, affording CO2‐polyols with ULMW (580 g mol−1) and high polymer selectivity (>99 %). Moreover, the ULMW CO2‐polyols with various architectures (tri‐, quadra‐, and hexa‐arm) can be obtained, suggesting the wide proton universality of supported catalysts. Notably, benefiting from the heterogeneous nature of the supported catalyst, colorless products can be facilely achieved by simple filtration. The present strategy provides a platform for the synthesis of colorless ULMW polyols derived from not only CO2/epoxides, but also lactone, anhydrides etc. or their combinations. [ABSTRACT FROM AUTHOR]

Activatable photosensitizers (PSs) have been widely used for the simultaneous fluorescence imaging and photodynamic ablation of cancer cells. However, the ready aggregation of traditional PSs in aqueous media can lead to fluorescence quenching as well as reduced phototoxicity even in the activated form. We have developed a series of PSs that show aggregation-enhanced emission and phototoxicity and thus the exact opposite behavior to that of previously reported PSs. We further developed a dual-targeted enzyme-activatable bioprobe based on the optimized photosensitizer and describe simultaneous light-up fluorescence imaging and activated photodynamic therapy for specific cancer cells. The design of smart probes should thus open new opportunities for targeted and image-guided photodynamic therapy. [ABSTRACT FROM AUTHOR]