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Zong Q, Zhou S, Ye J, Peng X, Wu H, Li M, Ye X, Tian N, Sun W, Zhai Y. Aliphatic polycarbonate-based hydrogel dressing for wound healing. Journal of Drug Delivery Science and Technology 2023;79:104083. [DOI: 10.1016/j.jddst.2022.104083] [Reference Citation Analysis]
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Oh J, Khan A. Main-Chain Polysulfonium Salts: Development of Non-Ammonium Antibacterial Polymers Similar in Their Activity to Antibiotic Drugs Vancomycin and Kanamycin. Biomacromolecules 2021;22:3534-42. [PMID: 34251178 DOI: 10.1021/acs.biomac.1c00627] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
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Zhu S, Xue R, Yu Z, Zhang X, Luan S, Tang H. Transition of Conformation and Solubility in β-Sheet-Structured Poly(l-cysteine)s with Methylthio or Sulfonium Pendants. Biomacromolecules 2021;22:1211-9. [PMID: 33533606 DOI: 10.1021/acs.biomac.0c01715] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
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Jimaja S, Xie Y, Foster JC, Taton D, Dove AP, O'reilly RK. Functional nanostructures by NiCCo-PISA of helical poly(aryl isocyanide) copolymers. Polym Chem 2021;12:105-12. [DOI: 10.1039/d0py00791a] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
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Jiang Y, Dong S, Qin G, Liu L, Zhao H. Oxidation and ATP dual-responsive block copolymer containing tertiary sulfoniums: self-assembly, protein complexation and triggered release. Polym Chem 2021;12:1125-35. [DOI: 10.1039/d0py01622e] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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Dong Y, Zhou J, Wang C, Wang Y, Deng L, Zhang J, Dong A. Comb‐Like Amphiphilic Polycarbonates with Different Lengths of Cationic Branches for Enhanced siRNA Delivery. Macromol Biosci 2020;20:2000143. [DOI: 10.1002/mabi.202000143] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
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Yeo H, Khan A. Photoinduced Proton-Transfer Polymerization: A Practical Synthetic Tool for Soft Lithography Applications. J Am Chem Soc 2020;142:3479-88. [PMID: 32040308 DOI: 10.1021/jacs.9b11958] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 8.7] [Reference Citation Analysis]
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Gao L, Dong B, Zhang J, Chen Y, Qiao H, Liu Z, Chen E, Dong Y, Cao C, Huang D, Chen W. Functional Biodegradable Nitric Oxide Donor-Containing Polycarbonate-Based Micelles for Reduction-Triggered Drug Release and Overcoming Multidrug Resistance. ACS Macro Lett 2019;8:1552-8. [PMID: 35619381 DOI: 10.1021/acsmacrolett.9b00758] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 6.0] [Reference Citation Analysis]
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Yan B, Hou J, Wei C, Xiao Y, Lang M, Huang F. Synthesis of main chain sulfur-containing aliphatic polycarbonates by organocatalytic ring-opening polymerization of macrocyclic carbonates. Polym Chem 2019;10:5191-9. [DOI: 10.1039/c9py01205b] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
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Hwang J, Lee DG, Yeo H, Rao J, Zhu Z, Shin J, Jeong K, Kim S, Jung HW, Khan A. Proton Transfer Hydrogels: Versatility and Applications. J Am Chem Soc 2018;140:6700-9. [DOI: 10.1021/jacs.8b03514] [Cited by in Crossref: 30] [Cited by in F6Publishing: 31] [Article Influence: 6.0] [Reference Citation Analysis]
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Wei C, Xu Y, Yan B, Hou J, Du Z, Lang M. Well-Defined Selenium-Containing Aliphatic Polycarbonates via Lipase-Catalyzed Ring-Opening Polymerization of Selenic Macrocyclic Carbonate Monomer. ACS Macro Lett 2018;7:336-40. [PMID: 35632908 DOI: 10.1021/acsmacrolett.8b00039] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 6.8] [Reference Citation Analysis]
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Zhang J, Li M, Cheng L, Li T. Self-Healable and Tough Thermoplastic Materials from Metal-Thioether Block Polymers. Macromol Chem Phys 2018;219:1700430. [DOI: 10.1002/macp.201700430] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
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Ge C, Zhao L, Ling Y, Tang H. Thermo and pH dual responsive polypeptides derived from “clickable” poly(γ-3-methylthiopropyl- l -glutamate). Polym Chem 2017;8:1895-905. [DOI: 10.1039/c7py00170c] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
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Zhang J, Li M, Cheng L, Li T. Multifunctional polymers built on copper–thioether coordination. Polym Chem 2017;8:6527-33. [DOI: 10.1039/c7py01359k] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 2.7] [Reference Citation Analysis]
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