Letteratura scientifica selezionata sul tema "RAFT photo-polymerization"
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Articoli di riviste sul tema "RAFT photo-polymerization":
Hartlieb, Matthias. "Photo‐Iniferter RAFT Polymerization". Macromolecular Rapid Communications 43, n. 1 (19 novembre 2021): 2100514. http://dx.doi.org/10.1002/marc.202100514.
Hartlieb, Matthias. "Photo‐Iniferter RAFT Polymerization". Macromolecular Rapid Communications 43, n. 1 (gennaio 2022): 2270003. http://dx.doi.org/10.1002/marc.202270003.
Li, Jiajia, Xiangqiang Pan, Na Li, Jian Zhu e Xiulin Zhu. "Photoinduced controlled radical polymerization of methyl acrylate and vinyl acetate by xanthate". Polymer Chemistry 9, n. 21 (2018): 2897–904. http://dx.doi.org/10.1039/c8py00050f.
Jiang, Ruming, Meiying Liu, Qiang Huang, Hongye Huang, Qing Wan, Yuanqing Wen, Jianwen Tian, Qian-yong Cao, Xiaoyong Zhang e Yen Wei. "Fabrication of multifunctional fluorescent organic nanoparticles with AIE feature through photo-initiated RAFT polymerization". Polymer Chemistry 8, n. 47 (2017): 7390–99. http://dx.doi.org/10.1039/c7py01563a.
Zhang, Junle, Mengya Li, Yanjie He, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Xiaoguang Qiao, Qingxiang Zhao e Xinchang Pang. "From 0-dimension to 1-dimensions: Au nanocrystals as versatile plasmonic photocatalyst for broadband light induced RAFT polymerization". Polymer Chemistry 12, n. 16 (2021): 2439–46. http://dx.doi.org/10.1039/d1py00088h.
Quan, Qinzhi, Honghong Gong e Mao Chen. "Preparation of semifluorinated poly(meth)acrylates by improved photo-controlled radical polymerization without the use of a fluorinated RAFT agent: facilitating surface fabrication with fluorinated materials". Polymer Chemistry 9, n. 30 (2018): 4161–71. http://dx.doi.org/10.1039/c8py00990b.
An, Nankai, Xi Chen e Jinying Yuan. "Non-thermally initiated RAFT polymerization-induced self-assembly". Polymer Chemistry 12, n. 22 (2021): 3220–32. http://dx.doi.org/10.1039/d1py00216c.
Wang, Wulong, Sheng Zhong, Guicheng Wang, Hongliang Cao, Yun Gao e Weian Zhang. "Photo-controlled RAFT polymerization mediated by organic/inorganic hybrid photoredox catalysts: enhanced catalytic efficiency". Polymer Chemistry 11, n. 18 (2020): 3188–94. http://dx.doi.org/10.1039/d0py00171f.
Chen, Mao, Honghong Gong e Yu Gu. "Controlled/Living Radical Polymerization of Semifluorinated (Meth)acrylates". Synlett 29, n. 12 (18 aprile 2018): 1543–51. http://dx.doi.org/10.1055/s-0036-1591974.
Cabannes-Boué, Benjamin, Qizhi Yang, Jacques Lalevée, Fabrice Morlet-Savary e Julien Poly. "Investigation into the mechanism of photo-mediated RAFT polymerization involving the reversible photolysis of the chain-transfer agent". Polymer Chemistry 8, n. 11 (2017): 1760–70. http://dx.doi.org/10.1039/c6py02220k.
Tesi sul tema "RAFT photo-polymerization":
Allegrezza, Michael LeGrande. "Mechanistic Insight Into Photo-Polymerization Techniques Through Kinetic Analysis". Miami University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=miami1605182244121264.
Ikkene, Djallal. "Glyco-nanostructures formulées via autoassemblage induit par photo-polymérisation RAFT en dispersion aqueuse". Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0035.
Soft nanostructures obtained by the self-assembly of amphiphilic copolymers (ACP) are of great relevance for nanomedecine, where they can be used as Drug Delivery Systems (DDSs). Among these DDSs, those with vesicular morphology (polymersomes) are under intense scrutiny, thanks to their interesting multi-compartmental morphology allowing the simultaneous encapsulation of both hydrophilic and hydrophobic drugs. Amphiphilic glycopolymers (AGPs), amphiphilic copolymers associating hydrophilic polysaccharides and hydrophobic polymers, are potential candidates for the formulation of DDSs due to the biodegradability, non-toxicity and tunable biocompatibility of polysaccharides. However, spherical micelles and core/shell nanoparticles have been frequently reported in case of the self-assembly of AGPs, which could be a limitation to their development. Herein, an emerging one-pot methodology named Polymerization-Induced Self-Assembly (PISA) in aqueous dispersion, enables producing self-assembled polymeric nanostructures directly in aqueous media, was used to fill the lack of AGPs in terms of self-assembly. More precisely, in the framework of this Ph.D., a water-soluble monomer (2-hydroxypropyl methacrylate, HPMA), forming a hydrophobic polymer, is polymerized from a water-soluble dextran derivative containing multiple chain transfer agent groups (DexCTA). Photo-mediated reversible addition-fragmentation chain transfer (photo-RAFT) was used to grow hydrophobic grafts of PHPMA from DexCTA to produce dextran-gN-PHPMAx, where N and X are respectively the number and the degree of polymerization of PHPMA grafts. As the PHPMA grafts increase, the glycopolymers become amphiphilic inducing its self-assembly to form glyco-nanostructures (GNSs). A deep physico-chemical investigation on such GNSs was carried out using advanced techniques, including radiation scattering (scattering of light, neutrons and small angle X-rays) and imaging techniques such as (cryo-) transmission electron microscopy (cryo-) TEM. This investigation revealed the ability of dextran-gN-PHPMAX to form nano-objects of advanced morphology (including vesicular one) in water via PISA process. These first observations encouraged us to study the impact of the macromolecular parameters of these AGPs (number and size of grafts) and the experimental conditions (weight concentration and temperature) on the generated self-assembly morphology. In-situ monitoring of the morphology evolution during the PISA revealed the formulation of an original morphology (multi-hydrophilic core vesicles) never reported in case of AGPs. The use of dextran-gN-PHPMAX-based vesicles as DSSs was evaluated by examining: i) the cytotoxicity of such AGPs toward various cell models, ii) their stability in various hypotonic and hypertonic environments miming biologic media, iii) and their ability to encapsulate hydrophilic and hydrophobic drugs