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Creators/Authors contains: "Fan, Yingjie"

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  1. ; (, Carbon Future)
    Full Text Available 
  2. ; ; ; ; ; ; (, ACS Catalysis)
    Free, publicly-accessible full text available November 15, 2025
  3. ; ; ; ; ; ; (, Angewandte Chemie International Edition)
    Abstract Abnormal cancer metabolism causes hypoxic and immunosuppressive tumor microenvironment (TME), which limits the antitumor efficacy of photodynamic therapy (PDT). Herein, we report a photosensitizing nanoscale metal–organic layer (MOL) with anchored 3‐bromopyruvate (BrP), BrP@MOL, as a metabolic reprogramming agent to enhance PDT and antitumor immunity. BrP@MOL inhibited mitochondrial respiration and glycolysis to oxygenate tumors and reduce lactate production. This metabolic reprogramming enhanced reactive oxygen species generation during PDT and reshaped the immunosuppressive TME to enhance antitumor immunity. BrP@MOL‐mediated PDT inhibited tumor growth by >90 % with 40 % of mice being tumor‐free, rejected tumor re‐challenge, and prevented lung metastasis. Further combination with immune checkpoint blockade potently regressed the tumors with >98 % tumor inhibition and 80 % of mice being tumor‐free. 
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  4. ; ; ; ; (, ACS Catalysis)
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  5. ; ; ; (, Chemical Science)
    A COF-based catalyst was synthesized to activate C–H bonds for C–C/C–N coupling via hydrogen atom transfer. The catalyst can be easily recycled, allowing downstream modification of the product to realize C–H to C–N/C–S/C–O transformations. 
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  6. ; ; ; (, Journal of the American Chemical Society)
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  7. ; ; ; (, Journal of the American Chemical Society)
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  8. ; ; ; (, Journal of the American Chemical Society)
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  9. ; ; ; (, Journal of the American Chemical Society)
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  10. ; ; ; ; (, Angewandte Chemie International Edition)
    Abstract Phosphine‐ligated transition metal complexes play a pivotal role in modern catalysis, but our understanding of the impact of ligand counts on the catalysis performance of the metal center is limited. Here we report the synthesis of a low‐coordinate mono(phosphine)‐Rh catalyst on a metal‐organic layer (MOL), P‐MOL • Rh, and its applications in the hydrogenation of mono‐, di‐, and tri‐substituted alkenes as well as aryl nitriles with turnover numbers (TONs) of up to 390000. Mechanistic investigations and density functional theory calculations revealed the lowering of reaction energy barriers by the low steric hindrance of site‐isolated mono(phosphine)‐Rh sites on the MOL to provide superior catalytic activity over homogeneous Rh catalysts. The MOL also prevents catalyst deactivation to enable recycle and reuse of P‐MOL • Rh in catalytic hydrogenation reactions. 
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