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通过锰掺杂增强手性碳点的本征氧化酶样活性用于选择性催化氧化。

Enhanced the intrinsic oxidase-like activity of chiral carbon dots via manganese doping for selective catalytic oxidation.

机构信息

Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, Jiangsu, China.

Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, Jiangsu, China; Macao Institute of Materials Science and Engineering (MIMSE), MUST-SUDA Joint Research Center for Advanced Functional Materials, Macau University of Science and Technology, Taipa 999078, Macao.

出版信息

J Colloid Interface Sci. 2024 Apr;659:687-696. doi: 10.1016/j.jcis.2024.01.039. Epub 2024 Jan 6.

Abstract

It is highly desirable to design and construct chemical catalysts with high activity and specificity as the alternatives of natural enzymes for industrial application. Chiral carbon dots (CDs), possessing both the intrinsic enzyme-like activity and specific recognition ability, are one of good candidates for enzyme-like catalysts. However, their catalytic activity is far from that of natural enzymes and needs to be enhanced. In this work, the modulation of the chiral structure and catalytic activity of chiral CDs with intrinsic oxidase-like activity was implemented by manganese (Mn) doping. Under the light condition, chiral CDs (l-Ser-CDs and d-Ser-CDs) derived from chiral serine (Ser) show weak catalytic activity and low selectivity toward the oxidation of L type of dopamine (l-DOPA), whereas the Mn functionalized chiral CDs (l-Mn-CDs or d-Mn-CDs) exhibit 6.9 times higher in catalytic activity and 2.9 times in selectivity ratio (SR) than Ser-CDs. Mn-CDs involve two-path catalytic process, in which the photogenerated electrons could reduce O to O as the active species and the holes would oxidize DOPA directly. Moreover, doping of Mn enables the CDs to generate more O. Besides, l-Mn-CDs have higher catalytic activity than that of d-Mn-CDs (+54.2 %), and the chiral Mn-CDs have stronger selective adsorption capacity towards chiral DOPA than Ser-CDs. Our work provides a new method for designing and preparing novel chiral artificial enzymes.

摘要

设计和构建具有高活性和高特异性的化学催化剂,以替代天然酶用于工业应用,这是非常理想的。手性碳点(CDs)具有内在的类酶活性和特异性识别能力,是类酶催化剂的良好候选者之一。然而,它们的催化活性远不及天然酶,需要加以提高。在这项工作中,通过锰(Mn)掺杂来调节具有内在氧化酶样活性的手性 CD 的手性结构和催化活性。在光照条件下,来源于手性丝氨酸(Ser)的手性 CD(l-Ser-CDs 和 d-Ser-CDs)对 L 型多巴胺(l-DOPA)的氧化表现出较弱的催化活性和较低的选择性,而功能化的 Mn 手性 CD(l-Mn-CDs 或 d-Mn-CDs)的催化活性比 Ser-CDs 高 6.9 倍,选择性比 Ser-CDs 高 2.9 倍。Mn-CDs 涉及双路径催化过程,其中光生电子可将 O 还原为 O 作为活性物质,而空穴可直接将 DOPA 氧化。此外,Mn 的掺杂使得 CDs 能够产生更多的 O。此外,l-Mn-CDs 的催化活性高于 d-Mn-CDs(+54.2%),且手性 Mn-CDs 对手性 DOPA 的选择性吸附能力强于 Ser-CDs。我们的工作为设计和制备新型手性人工酶提供了一种新方法。

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