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首页> 外文期刊>Scientific reports. >C70 Fullerene Cage as a Novel Catalyst for Efficient Proton Transfer Reactions between Small Molecules: A Theoretical study
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C70 Fullerene Cage as a Novel Catalyst for Efficient Proton Transfer Reactions between Small Molecules: A Theoretical study

机译:C70富勒烯笼作为小分子之间有效质子转移反应的新型催化剂:理论研究

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When acids are supplied with an excess electron (or placed in an Ar or the more polarizable Nsub2/sub matrix) in the presence of species such as NHsub3/sub, the formation of ion-pairs is a likely outcome. Using density functional theory and first-principles calculations, however, we show that, without supplying an external electron or an electric field, or introducing photo-excitation and -ionization, a single molecule of HCl or HBr in the presence of a single molecule of water inside a Csub70/sub fullerene cage is susceptible to cleavage of the σ-bond of the Br?nsted-Lowry acid into Xsup-/sup and Hsup+/sup ions, with concomitant transfer of the proton along the reaction coordinate. This leads to the formation of an Xsup-/sup···sup+/supHOHsub2/sub (X?=?Cl, Br) conjugate acid-base ion-pair, similar to the structure in water of a Zundel ion. This process is unlikely to occur in other fullerene derivatives in the presence of Hsub2/subO without significantly affecting the geometry of the carbon cage, suggesting that the interior of Csub70/sub is an ideal catalytic platform for proton transfer reactions and the design of related novel materials. By contrast, when a single molecule of HF is reacted with a single molecule of Hsub2/subO inside the Csub70/sub cage, partial proton transfers from HF to Hsub2/subO is an immediate consequence, as recently observed experimentally. The geometrical, energetic, electron density, orbital, optoelectronic and vibrational characteristics supporting these observations are presented. In contrast with the views that have been advanced in several recent studies, we show that the encaged species experiences significant non-covalent interaction with the interior of the cage. We also show that the inability of current experiments to detect many infrared active vibrational bands of the endo species in these systems is likely to be a consequence of the substantial electrostatic screening effect of the cage.
机译:当酸被提供过量的电子(或置于AR或更可极化的N 2 2 / sub>基质中时),如NH 3 的存在,形成离子的形成-PAIRS是一个可能的结果。然而,使用密度函数理论和第一原理计算,我们表明,在不提供外部电子或电场的情况下,或在单个分子存在下引入光激发和引入光激发和离子,单个HCl或HBr C 70 富勒烯笼内的水易于将Brαnsted-lowry酸的σ-键切割成x - 和h + 离子,伴随着沿反应坐标的质子的转移。这导致形成X - ··· + hoh 2 (x≤=Δcl,br)缀合酸碱离子-Pair,类似于Zundel离子水中的结构。在H 2 o存在下,在存在的其他富勒烯衍生物中不太可能发生该过程,而不会显着影响碳笼的几何形状,这表明C 70 的内部是一个理想的质子转移反应催化平台和相关新型材料的设计。相反,当单一分子的HF与C 70 笼内的单个分子H 2℃反应时,部分质子转移来自HF到H 2 o是一项直接后果,正如实验所观察到的那样。提出了支持这些观察结果的几何,能量,电子密度,轨道,光电和振动特性。相反,与最近的几项研究中提出的观点相比,我们表明,所摄像的物种经历了与笼子内部的显着非共价互动。我们还表明,在这些系统中检测到内诺种类的许多红外主动振动带的无法能力可能是笼子的大致静电筛选效果的结果。

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