NIR-accelerated cascade reaction for degradation of organophosphorus compounds by Au/PTE/ZIF-8: cooperative effect and mechanism†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Fang Wang , Yi Ouyang , Pengfei Zhou , Yan Zhang , Renjun Gao , Bekir Engin Eser , Zheng Guo
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Abstract

Herein, we designed a NIR (near-infrared)-responsive multifunctional nanoreactor that can be used for precise and immediate regulation of chemoenzymatic degradation of organophosphates (OPs). The thermophilic phosphotriesterases (PTEs) and gold nanoparticles (AuNPs) were encapsulated in the ZIF-8 structure yielding an Au/PTE/ZIF-8 nanocomposite, which can be modulated by NIR as a result of the photothermal effect of AuNPs. The Au/PTE/ZIF-8 nanoreactor demonstrated excellent performance in mediating cascade reactions from enzymatic hydrolysis of OPs (>90% conversion in 10 min) to the subsequent reduction of the resulting 4-nitrophenol (4-NP) into 4-aminophenol (4-AP) by NaBH4 (>90% yield of 4-AP in 30 min). An immediate light-to-heat conversion when NIR was applied to Au/PTE/ZIF-8 at room temperature enables a 2-fold increase in the specific activity of phosphotriesterase from S. islandicus compared to thermo-heating at 70 °C. Based on the fact that there was a significant acceleration in 4-NP reduction by Au/PTE/ZIF-8, we proposed a plausible reaction mechanism (reaction pathway) suggesting that: 1) cooperative actions between Au, ZIF-8 and substrates take place by promoting polarization and cleavage of the B–H bond in NaBH4 for releasing hydride facilitating electron and hydride transfer to 4-NP; and 2) stabilizing the formation of intermediates or the transition state by coordination with a ZIF-8 delocalized network and/or Au.

Abstract Image

Abstract Image

金/PTE/ZIF-8降解有机磷化合物的近红外加速级联反应:协同效应与机理
在此,我们设计了一种近红外(NIR)响应型多功能纳米反应器,可用于对有机磷酸酯(OPs)的化学降解进行精确和即时的调节。嗜热磷酸酯酶(PTEs)和金纳米粒子(AuNPs)被封装在 ZIF-8 结构中,形成了 Au/PTE/ZIF-8 纳米复合材料,由于 AuNPs 的光热效应,该复合材料可通过近红外进行调节。Au/PTE/ZIF-8 纳米反应器在介导级联反应方面表现出色,从酶水解 OPs(10 分钟内转化率达 90%)到随后 NaBH4 将生成的 4-硝基苯酚(4-NP)还原为 4-氨基苯酚(4-AP)(30 分钟内 4-AP 生成率达 90%)。在室温下将近红外照射到 Au/PTE/ZIF-8 上时,可立即实现光热转换,与 70 °C 的热加热相比,岛菌磷酸酯酶的比活性提高了 2 倍。基于 Au/PTE/ZIF-8 显著加速了 4-NP 的还原这一事实,我们提出了一种合理的反应机制(反应途径),即:1)Au、PTE 和 ZIF-8 之间的协同作用;2)Au、PTE 和 ZIF-8 之间的协同作用;3)Au、PTE 和 ZIF-8 之间的协同作用:1) 金、ZIF-8 和底物之间通过促进极化和裂解 NaBH4 中的 B-H 键来释放氢化物,从而促进电子和氢化物转移到 4-NP 上;以及 2) 通过与 ZIF-8 脱定位网络和/或金配位来稳定中间体或过渡态的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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