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。
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.