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Synthesis of dimethacrylates monomers with low polymerization shrinkage and its application in dental composites materials

机译:低聚合收缩率的二甲基丙烯酸酯单体的合成及其在牙科复合材料中的应用

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In this work, a new dimethacrylate monomer named a,a'-Bis(4-(2'-hydroxy- 3'methacryloyloxy-propoxy)- 3,5-dimethylphenyl)-1,4-diisopropyl-benzene (a,a'- BHMPDDB) was synthesized to replace 2,2-bis[4-(2'-hydroxy- 3'-methacryloyloxy- propoxy)-phenyl]propane (Bis- GMA) as one component of dental composite materials. The structures of a,a'-BHMPDDB and its intermediate product a,a'-Bis(4-oxiranylmethoxy-3,5-dimethylphenyl)-1,4-diisopropylbenzene (a,a'-BODDB) were confirmed by FT-IR, 1HNMR, and elemental analysis. a,a'-BHMPDDB was mixed with TEGDMA to form a new dental resin, and double bond conversion, polymerization shrinkage, contact angle, water sorption and solubility, flexural strength and modulus before and after water immersion of this new dental resin were studied. Compared with the commonly used Bis-GMA/ TEGDMA dental resin, a,a'-BHMPDDB/TEGDMA had higher double bond conversion (60.5±0.3%), lower polymerization shrinkage (5.6 %), and comparable flexural strength before water immersion (94.1±3.9 MPa), which made a,a'- BHMPDDB/TEGDMA having potential to replace Bis- GMA/TEGDMA as matrix phase of dental composites materials. However, a,a'-BHMPDDB/TEGDMA also had drawbacks, such as higher water sorption (5.06±0.17 %), water solubility (2.37±0.1 %), and lower flexural strength after water immersion (71.4±14.6 MPa).
机译:在这项工作中,一种新的二甲基丙烯酸酯单体称为a,a'-双(4-(2'-羟基-3'甲基丙烯酰氧基-丙氧基)-3,5-二甲基苯基)-1,4-二异丙基苯(a,a' -合成了BHMPDDB)以代替2,2-双[4-(2'-羟基-3'-甲基丙烯酰氧基-丙氧基)-苯基]丙烷(Bis-GMA)作为牙科复合材料的一种组分。 FT-IR证实了a,a'-BHMPDDB及其中间产物a,a'-Bis(4-环氧乙烷基甲氧基-3,5-二甲基苯基)-1,4-二异丙基苯(a,a'-BODDB)的结构,1 HNMR和元素分析。将a,a'-BHMPDDB与TEGDMA混合形成一种新型牙科树脂,并研究了该新型牙科树脂在水浸之前和之后的双键转化率,聚合收缩率,接触角,吸水率和溶解度,弯曲强度和模量。与常用的Bis-GMA / TEGDMA牙科树脂相比,a,a'-BHMPDDB / TEGDMA具有更高的双键转化率(60.5±0.3%),更低的聚合收缩率(5.6%)和相当的水浸前抗弯强度(94.1) ±3.9 MPa),这使得a,a'- BHMPDDB / TEGDMA有潜力替代Bis-GMA / TEGDMA作为牙科复合材料的基质相。然而,a,a′-BHMPDDB / TEGDMA也具有缺点,例如较高的吸水率(5.06±0.17%),水溶性(2.37±0.1%)和较低的水浸后抗弯强度(71.4±14.6MPa)。

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