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4-巯基苯硼酸和过氧化氢以两种不同方式导致金纳米颗粒聚集。

Aggregation of Gold Nanoparticles Caused in Two Different Ways Involved in 4-Mercaptophenylboronic Acidand Hydrogen Peroxide.

作者信息

Li Runmei, Gu Xuefan, Liang Xingtang, Hou Shi, Hu Daodao

机构信息

Engineering Research Center of Historical and Cultural Heritage Protection, Ministry of Education, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an 710062, China.

College of Chemistry and Chemical Engineering, Xi'an Shiyou University, Xi'an 710065, China.

出版信息

Materials (Basel). 2019 Jun 3;12(11):1802. doi: 10.3390/ma12111802.

Abstract

The difference in gold nanoparticle (AuNPs) aggregation caused by different mixing orders of AuNPs, 4-mercaptophenylboronic acid (4-MPBA), and hydrogen peroxide (HO) has been scarcely reported. We have found that the color change of a ((4-MPBA + AuNPs) + HO) mixture caused by HO is more sensitive than that of a ((4-MPBA + HO) + AuNPs) mixture. For the former mixture, the color changes obviously with HO concentrations in the range of 00.025%. However, for the latter mixture, the corresponding HO concentration is in the range of 01.93%. The mechanisms on the color change originating from the aggregation of AuNPs occurring in the two mixtures were investigated in detail. For the ((4-MPBA + HO) + AuNPs) mixture, free 4-MPBA is oxidized by HO to form bis(4-hydroxyphenyl) disulfide (BHPD) and peroxoboric acid. However, for the ((4-MPBA+AuNPs) + HO) mixture, immobilized 4-MPBA is oxidized by HO to form 4-hydroxythiophenol (4-HTP) and boric acid. The decrease in charge on the surface of AuNPs caused by BHPD, which has alarger steric hindrance, is poorer than that caused by -4-HTP, and this is mainly responsible for the difference in the aggregation of AuNPs in the two mixtures. The formation of boric acid and peroxoboric acid in the reaction between 4-MPBA and HO can alter the pH of the medium, and the effect of the pH change on the aggregation of AuNPs should not be ignored. These findings not only offer a new strategy in colorimetric assays to expand the detection range of hydrogen peroxide concentrations but also assist in deepening the understanding of the aggregation of citrate-capped AuNPs involved in 4-MPBA and HO, as well as in developing other probes.

摘要

金纳米颗粒(AuNPs)、4-巯基苯硼酸(4-MPBA)和过氧化氢(HO)不同混合顺序导致的AuNPs聚集差异鲜有报道。我们发现,((4-MPBA + AuNPs)+ HO)混合物因HO引起的颜色变化比((4-MPBA + HO)+ AuNPs)混合物更敏感。对于前一种混合物,在00.025%的HO浓度范围内颜色明显变化。然而,对于后一种混合物,相应的HO浓度范围是01.93%。详细研究了两种混合物中因AuNPs聚集导致颜色变化的机制。对于((4-MPBA + HO)+ AuNPs)混合物,游离的4-MPBA被HO氧化形成双(4-羟基苯基)二硫化物(BHPD)和过硼酸。然而,对于((4-MPBA+AuNPs) + HO)混合物,固定化的4-MPBA被HO氧化形成4-羟基苯硫酚(4-HTP)和硼酸。空间位阻较大的BHPD导致AuNPs表面电荷减少的程度比-4-HTP导致的要差,这主要是两种混合物中AuNPs聚集差异的原因。4-MPBA与HO反应中硼酸和过硼酸的形成会改变介质的pH值,pH值变化对AuNPs聚集的影响不容忽视。这些发现不仅为比色测定提供了一种新策略以扩大过氧化氢浓度的检测范围,还有助于加深对参与4-MPBA和HO的柠檬酸盐包覆AuNPs聚集的理解,以及开发其他探针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21eb/6600739/c6acaecf7e90/materials-12-01802-g001.jpg

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