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Monitoring the Reactivity of Formamide on Amorphous SiO2 by In-Situ UV-Raman Spectroscopy and DFT Modeling

机译:通过原位紫外拉曼光谱和DFT建模监测甲酰胺在无定形SiO2上的反应性

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摘要

Formamide has been recognized in the literature as a key species in the formation of the complex molecules of life, such as nucleobases. Furthermore, several studies reported the impact of mineral phases as catalysts for its decomposition/polymerization processes, increasing the conversion and also favoring the formation of specific products. Despite the progresses in the field, in situ studies on these mineral-catalyzed processes are missing. In this work, we present an in situ UV-Raman characterization of the chemical evolution of formamide over amorphous SiO samples, selected as a prototype of silicate minerals. The experiments were carried out after reaction of formamide at 160 °C on amorphous SiO (Aerosil OX50) either pristine or pre-calcined at 450 °C, to remove a large fraction of surface silanol groups. Our measurements, interpreted on the basis of density functional B3LYP-D3 calculations, allow to assign the spectra bands in terms of specific complex organic molecules, namely, diaminomaleonitrile (DAMN), 5-aminoimidazole (AI), and purine, showing the role of the mineral surface on the formation of relevant prebiotic molecules.
机译:甲酰胺在文献中已被认为是生命复杂分子(如核碱基)形成中的关键物种。此外,一些研究报道了矿物相作为其分解/聚合过程催化剂的影响,增加了转化率,也有利于特定产物的形成。尽管在该领域取得了进展,但仍缺少对这些矿物催化过程的原位研究。在这项工作中,我们提出了甲酰胺在无定形SiO样品上的化学演化的原位UV-拉曼表征,该样品被选作硅酸盐矿物的原型。实验是在甲酰胺在160°C的原始二氧化硅上或在450°C下预煅烧的无定形SiO(Aerosil OX50)上反应,以除去大部分表面硅烷醇基团之后进行的。我们的测量基于密度泛函B3LYP-D3计算来解释,可以根据特定的复杂有机分子(即二氨基马腈(DAMN),5-氨基咪唑(AI)和嘌呤)分配光谱带,从而显示了矿物质表面上会形成相关的益生元分子。

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