...
首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >5,6-Dihydroxyindole-2-carboxylic-Acid-TiO2 Charge Transfer Complexes in the Radical Polymerization of Melanogenic Precursor(s)
【24h】

5,6-Dihydroxyindole-2-carboxylic-Acid-TiO2 Charge Transfer Complexes in the Radical Polymerization of Melanogenic Precursor(s)

机译:黑色素生成前体的自由基聚合反应中的5,6-二羟基吲哚-2-羧酸-TiO2电荷转移配合物

获取原文
获取原文并翻译 | 示例

摘要

A combination of biomedical and technological applications is generating, over the past decades, the well established interest toward melanins and melanogenesis. Several compounds have been explored to promote/catalyze oxidative polymerization of melanogenic precursors, such as 5,6-dihydroxyindole-2-carboxylic acid (DHICA), to melanin-like biopolymers in vitro. TiO2 has shown a photocatalytic activity driving DHICA polymerization and leading to the formation of melanin-TiO2 hybrid nanostructures with unique biocide behavior even under visible light. However, the mechanism of melanin formation in those hybrids is not yet well understood although a ligand to metal charge transfer (LMCT) process involving DHICA and Ti4+ ions was hypothesized. Here, we focus on melanin formation and apply a complementary analysis, by using photoluminescence (PL), UV-vis, electron paramagnetic resonance (EPR), and nuclear magnetic resonance (NMR) spectroscopy to reveal the mechanism of DHICA polymerization in the presence of a TiO2-sol. This study discloses TiO2 potentialities to drive and template DHICA polymerization to melanin via LMCT-based photo-oxidative process.
机译:在过去的几十年中,生物医学和技术应用的结合产生了对黑色素和黑色素生成的公认兴趣。已经探索了几种化合物在体外促进/催化黑色素生成前体例如5,6-二羟基吲哚-2-羧酸(DHICA)的氧化聚合为类黑色素生物聚合物。 TiO2具有光催化活性,可驱动DHICA聚合并导致形成黑色素-TiO2杂化纳米结构,即使在可见光下也具有独特的杀菌作用。然而,尽管假设了涉及DHICA和Ti4 +离子的配体到金属电荷转移(LMCT)过程,但尚未很好地理解这些杂种中黑色素的形成机理。在这里,我们专注于黑色素的形成,并通过使用光致发光(PL),紫外可见光,电子顺磁共振(EPR)和核磁共振(NMR)光谱进行补充分析,以揭示存在DHICA的机理。 TiO2-溶胶。这项研究揭示了通过基于LMCT的光氧化过程驱动TiO2并使其模板化至黑色素的TiO2潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号