掺杂 N 的碳点纳米共轭物中电子相互作用增强的 NO 光释放和光热转换。

Francesca Laneri, Cristina Parisi, Marta Maria Natile, Salvatore Sortino
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引用次数: 0

摘要

一种一氧化氮(NO)光诱导体(1)能够通过逐步机制释放出两个 NO 分子,它被共价接枝到蓝色发光的掺杂 N 的碳点(NCDs)上。由此产生的直径约为 10 纳米的水溶性纳米共轭物(NCDs-1)显示出一种新的吸收带,而这两种成分的简单物理混合物中并不存在,这归因于它们在基态时的强烈电子相互作用。蓝光激发 NCDs-1 会导致氮氧化物光生成,其效率几乎比单独观察到的 1 高一个数量级,这可能是由于 NCDs 和接枝 1 之间的光诱导电子转移。此外,与 1 相反,纳米共轭物在绿光激发下也能释放 NO。最后,NCDs 的典型蓝色荧光在 NCDs-1 中被淬灭,但在第二个 NO 分子的光弹作用下又会恢复,从而提供了有关光生成的 NO 量的可读和实时信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electronic interaction-enhanced NO photorelease and photothermal conversion in N-doped carbon dot nanoconjugates.

A nitric oxide (NO) photodonor (1) capable of releasing two NO molecules through a stepwise mechanism has been covalently grafted to blue-emitting N-doped carbon dots (NCDs). The resulting water-soluble nanoconjugate (NCDs-1), ca. 10 nm in diameter, exhibits a new absorption band not present in the simple physical mixture of the two components and is attributable to strong electronic interactions between them in the ground state. Blue light excitation of NCDs-1 leads to NO photogeneration with an efficiency almost one order of magnitude higher than that observed for 1 alone, probably due to a photoinduced electron transfer between the NCDs and the grafted 1. Photoexcitation of the nanoconjugate also results in effective photothermal conversion, which is negligible in the naked NCDs. Furthermore, in contrast to 1, the nanoconjugate liberates NO also under excitation with green light. Finally, the typical blue fluorescence of the NCDs is quenched in NCDs-1 but restored upon the photouncaging of the second NO molecule, providing readable and real-time information about the amount of NO photogenerated.

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来源期刊
Journal of materials chemistry. B
Journal of materials chemistry. B 化学科学, 工程与材料, 生命科学, 分析化学, 高分子组装与超分子结构, 高分子科学, 免疫生物学, 免疫学, 生化分析及生物传感, 组织工程学, 生物力学与组织工程学, 资源循环科学, 冶金与矿业, 生物医用高分子材料, 有机高分子材料, 金属材料的制备科学与跨学科应用基础, 金属材料, 样品前处理方法与技术, 有机分子功能材料化学, 有机化学
CiteScore
12.00
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1 months
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