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Synthesis and characterization of two novel antibacterial dendritic methacrylate-based dental monomers

机译:两种新型抗菌树突甲基丙烯酸酯类牙科单体的合成与表征

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This study explores the synthesis and characterization of two novel antibacterial dendritic methacrylate-based dental monomers. For this purpose, two dendritic esters have been synthesized via condensation reaction and then reacted with methacryloyl chloride to afford methacrylate-end caped dendritic esters. These compounds are subsequently converted to quaternary ammonium ?uoride monomers (QAFMs) with decyl substituted side chain to produce two novel antibacterial dendreticdental monomers. The chemical structures of synthesized samples have been characterized using Fourier transform infrared (FTIR) and proton nuclear magnetic resonance ( 1 H NMR) spectroscopies.The obtained monomers can be used to replace 2,2-bis[4-(2-hydroxy-3-methacryloyloxypropyl)-phenyl]propane (Bis-GMA) as the base monomer of universal resin-based dental composites in the presence of a diluting monomer ( e.g., triethyleneglycoldimethacrylate; TEGDMA), mainly due to their superior characteristics such as multifunctionalities as well as antibacterial activities.
机译:该研究探讨了两种新型抗菌树突甲基丙烯酸酯类牙科单体的合成和表征。为此目的,通过缩合反应合成了两个树突酯,然后与甲基丙烯酰氯反应,得到甲基丙烯酸酯端封闭的树突酯。随后将这些化合物与癸基取代的侧链转化为季铵的单体(QAFM)以产生两种新型抗菌树枝状单体。合成样品的化学结构已经用傅里叶变换红外(FTIR)和质子核磁共振(1 H NMR)光谱特征。所得单体可用于代替2,2-双[4-(2-羟基-3 - 甲基丙烯酰氧基丙基) - 苯基]作为稀释单体(例如三乙烯基丙烯二甲基丙烯酸酯; TEGDMA)存在的通用树脂基牙科复合材料的基础单体,主要是由于它们的优异特性,如多功能和多功能抗菌活性。

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