Li Zhang on Muck Rack

Li Zhang

  • College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou China
China
As seen in: Color Research & Application, Wiley, Wiley Online Library, British Pharmacological Society, New Phytologist, ACS Publications, Refinery29, JNeurosci, American Society for Microbiology (ASM), The Journal of Biological Chemistry and
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Articles

Curing-Induced Nanophase Engineering in Boronic-Ester Epoxy Vitrimers for Low-Loss, High-Breakdown, and Stress-Relaxed Insulation

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By Yiwei Wang, Li Zhang, Qingsong Liu
| Wiley Online Library Verified
, , , , , and , “Curing-Induced Nanophase Engineering in Boronic-Ester Epoxy Vitrimers for Low-Loss, High-Breakdown, and Stress-Relaxed Insulation.” Advanced Functional Materials (2026): e76568. https://doi.org/10.1002/adfm.76568 Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Charge-Directed Photothermal Methane Dry Reforming Enabled by Interfacial TiO x Nanodomains

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By Bifang Li, Li Zhang, Bo Su
| Wiley Online Library Verified
, , and et al., ““Charge-Directed Photothermal Methane Dry Reforming Enabled by Interfacial TiOx Nanodomains,” Angewandte Chemie International Edition ((2026): e4126002, https://doi.org/10.1002/anie.4126002 Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Light-Driven Epimerization: Diastereoconvergent Synthesis of [ 12 C, 13 C] β 2,3 -Amino Acids

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By Li Zhang, Yaxin Sun, Haiping Yu
| Wiley Online Library Verified
1 Introduction β-Amino acids serve as fundamental building blocks of life and perform vital functions in the fields of drug manufacturing, biochemistry, and organic synthesis [1-3]; notably, the C2, C3-disubstituted β2,3-amino acids could form more rigid spatial structures when incorporated into peptide chains [4, 5]. Typically, the spatial conformations of foldamers composed of β2,3-amino acids vary with their stereochemistry.
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