S Mahesh, Narasaiah Boya Palajonnala, B Himabindu, G L Balaji, Pradeepkiran Jangampalli Adi, Padhy Harihara
PG&Research Department of Chemistry, Thanthai Hans Roever Collage (Autonomous), Affiliated to Bharathidasan University, Perambalur 621220, India.
Department of Physics, Indian Institute of Technology (IIT), Tirupati 517506, India.
Antioxidants (Basel). 2022 Mar 31;11(4):688. doi: 10.3390/antiox11040688.
The present report presents a green method for the rapid biogenic synthesis of nanoparticles that offers several advantages over the current chemical and physical procedures. It is easy and fast, eco-friendly, and does not involve any precious elements, hazardous chemicals, or harmful solvents. The synthesized ZnO nanoparticles were characterized using different techniques, such as UV-Visible spectroscopy. The surface plasmon resonance confirmed the formation of ZnO nanoparticles at 344 nm, using UV-Visible spectroscopy. The leaf extract acts as a source of phytochemicals and is primarily used for the reduction and then the formation of stable ZnO nanoparticles by the characteristic functional groups of the extract; the synthesized ZnO nanoparticles were identified using FTIR spectroscopy. The crystalline nature of ZnO-NPs was confirmed via powder X-ray diffraction (XRD). Size and morphology were measured via high resolution transmission electron microscopy (HR-TEM) analysis. The stability of the nanoparticles is established using dynamic light scattering (DLS) and thermogravimetric analysis (TGA). The synthesized ZnO nanoparticles have been found to be a good and efficient catalyst for the synthesis of novel 1,2-dihydro quinazoline derivatives under the green method via a one-pot reaction of 2-amino benzophenone, 1,3-diphenyl-1H-pyrazole carbaldehydes, and ammonium acetate. The synthesized compounds (-) were characterized by the H NMR, C NMR, and HRMS spectra and were further validated for free-radical scavenging activity. The synthesized ZnO nanoparticles exhibited good antioxidant activity.
本报告介绍了一种绿色方法,用于快速生物合成纳米颗粒,该方法比目前的化学和物理方法具有多个优势。它简便快捷、环保,且不涉及任何贵金属元素、危险化学品或有害溶剂。使用不同技术对合成的氧化锌纳米颗粒进行了表征,如紫外可见光谱法。表面等离子体共振通过紫外可见光谱法证实了在344 nm处形成了氧化锌纳米颗粒。叶提取物作为植物化学物质的来源,主要用于还原,然后通过提取物的特征官能团形成稳定的氧化锌纳米颗粒;使用傅里叶变换红外光谱法对合成的氧化锌纳米颗粒进行了鉴定。通过粉末X射线衍射(XRD)证实了氧化锌纳米颗粒的晶体性质。通过高分辨率透射电子显微镜(HR-TEM)分析测量了尺寸和形态。使用动态光散射(DLS)和热重分析(TGA)确定了纳米颗粒的稳定性。已发现合成的氧化锌纳米颗粒是一种良好且高效的催化剂,可通过2-氨基二苯甲酮、1,3-二苯基-1H-吡唑甲醛和醋酸铵的一锅反应,在绿色方法下合成新型1,2-二氢喹唑啉衍生物。通过1H NMR、13C NMR和高分辨质谱(HRMS)光谱对合成的化合物进行了表征,并进一步验证了其自由基清除活性。合成的氧化锌纳米颗粒表现出良好的抗氧化活性。