Green Synthesis of Carbon Nanodots (CNDs) Moderated by Flavonoid Extracts from Moringa oleifera Leaves and Co-Doped Sulfur/Nitrogen (NS - CNDs - Fla) and Their Potential for Heavy Metals Sensing Application.

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Fluorescence Pub Date : 2024-09-25 DOI:10.1007/s10895-024-03931-2
Sriati Wahyudi, Ivan Rizoputra, Camellia Panatarani, Ferry Faizal, Ayi Bahtiar
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Abstract

Carbon nano dots (CNDs) has received a lot of attention in recent years due to their potential use in various kinds of applications. Many conventional chemical methods have been used to synthesis CNDs, but these processes have several drawbacks, such as hazardous by products, harsh chemicals, and high costs. To overcome these issues, green chemistry has an importance in the development of CNDs. Thus, it is essential to explore green synthesis approaches for production the CNDs. In this context, a novel precursor using flavonoid extraction from Moringa oleifera leaves is proposed. Moringa oleifera is the "magic tree" which contains many bioactive compounds such as flavonoids, especially in its leaves. Natural flavonoids and glycosides with specific components of structure can bind to metal ions. The content of bioactive compounds such as total flavonoids found in Moringa oleifera leaves is 172.10 mg/g. In addition, carbon (47.34%), nitrogen (51.67%), and sulfur (0.99%) are also the main composition. Then, the carbon nanodots (CNDs) synthesized in this research were moderated by flavonoid extract from Moringa oleifera using the hydrothermal method. The technique is easy, ecologically friendly, and requires neither specialized device or reagents. In practice, the CNDs produced are almost circular, with an average diameter of 3.49 nm. Furthermore, we enhanced synthesis CNDs - Fla with heteroatoms of nitrogen (N) and sulfur (S). They display a broad excitation-emission spectrum, excitation-dependent emission, and extraordinary fluorescence. Therefore, the synthesis of CNDs using flavonoids from Moringa oleifera as precursors would be a great potential candidate for the development of novel types of heavy metals sensing.

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用油辣木叶中的黄酮类提取物和共掺硫/氮(NS - CNDs - Fla)调制的碳纳米点(CNDs)的绿色合成及其在重金属传感方面的应用潜力。
近年来,碳纳米点(CNDs)因其在各种应用中的潜在用途而备受关注。许多传统化学方法已被用于合成 CND,但这些工艺存在一些缺点,如有害副产品、刺激性化学品和高成本。为了克服这些问题,绿色化学在 CND 的开发中具有重要意义。因此,探索生产 CND 的绿色合成方法至关重要。在此背景下,我们提出了一种利用从油辣木叶中提取黄酮类化合物的新型前体。油辣木是一种 "神奇的树",含有许多生物活性化合物,如黄酮类化合物,尤其是在其叶子中。具有特定结构成分的天然类黄酮和苷可与金属离子结合。油辣木叶中的生物活性化合物(如总黄酮)含量为 172.10 毫克/克。此外,碳(47.34%)、氮(51.67%)和硫(0.99%)也是主要成分。然后,本研究中合成的碳纳米点(CNDs)通过水热法从油橄榄中提取黄酮类化合物进行调节。该技术简单易行、生态友好,不需要专门的设备或试剂。实际上,生产出的 CND 几乎呈圆形,平均直径为 3.49 nm。此外,我们还增强了带有氮(N)和硫(S)杂原子的 CNDs - Fla 的合成。它们显示出宽广的激发-发射光谱、激发依赖性发射和非凡的荧光。因此,以油辣木中的黄酮类化合物为前体合成的 CNDs 将成为开发新型重金属传感技术的潜在候选物质。
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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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