Department of Chemistry, Universitat de les Illes Balears, Ctra. de Valldemossa km. 7.5, 07122 Palma de Mallorca, Islas Baleares, Spain.
Int J Mol Sci. 2024 Jun 11;25(12):6436. doi: 10.3390/ijms25126436.
In this study, FeO nanoparticles (FeNPs) decorated with halogenated perylene diimides (PDIs) have been used for capturing VOCs (volatile organic compounds) through noncovalent binding. Concretely, we have used tetrachlorinated/brominated PDIs as well as a nonhalogenated PDI as a reference system. On the other hand, methanol, ethanol, propanol, and butanol were used as VOCs. Experimental studies along with theoretical calculations (the BP86-D3/def2-TZVPP level of theory) pointed to two possible and likely competitive binding modes (lone pair-π through the π-acidic surface of the PDI and a halogen bond via the σ-holes at the Cl/Br atoms). More in detail, thermal desorption (TD) experiments showed an increase in the VOC retention capacity upon increasing the length of the alkyl chain, suggesting a preference for the interaction with the PDI aromatic surface. In addition, the tetrachlorinated derivative showed larger VOC retention times compared to the tetrabrominated analog. These results were complemented by several state-of-the-art computational tools, such as the electrostatic surface potential analysis, the Quantum Theory of Atoms in Molecules (QTAIM), as well as the noncovalent interaction plot (NCIplot) visual index, which were helpful to rationalize the role of each interaction in the VOC···PDI recognition phenomena.
在这项研究中,使用了被卤化苝二酰亚胺(PDI)修饰的 FeO 纳米粒子(FeNPs)通过非共价键捕获 VOC(挥发性有机化合物)。具体来说,我们使用了四氯化/溴化 PDI 以及非卤化 PDI 作为参考体系。另一方面,甲醇、乙醇、丙醇和丁醇被用作 VOC。实验研究和理论计算(BP86-D3/def2-TZVPP 理论水平)表明存在两种可能的竞争性结合模式(通过 PDI 的π-酸性表面的孤对-π 和通过 Cl/Br 原子的σ-孔的卤素键)。更详细地说,热解吸(TD)实验表明,随着烷基链长度的增加,VOC 保留容量增加,表明与 PDI 芳香表面的相互作用具有优先性。此外,四氯化衍生物与四溴化类似物相比,具有更大的 VOC 保留时间。这些结果得到了一些最先进的计算工具的补充,例如静电表面势能分析、原子在分子中的量子理论(QTAIM),以及非共价相互作用图(NCIplot)可视指标,这有助于合理说明每种相互作用在 VOC···PDI 识别现象中的作用。