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Controlled release of hydrogen isotope compounds and tunneling effect in the heterogeneously-catalyzed formic acid dehydrogenation

机译:在非均相催化的甲酸脱氢中控制氢同位素化合物和隧穿效应

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摘要

The hydrogen isotope deuterium is widely used in the synthesis of isotopically-labeled compounds and in the fabrication of semiconductors and optical fibers. However, the facile production of deuterium gas (Dsub2/sub) and hydrogen deuteride (HD) in a controlled manner is a challenging task, and rational heterogeneously-catalyzed protocols are still lacking. Herein, we demonstrate the selective production of hydrogen isotope compounds from a combination of formic acid and Dsub2/subO, through cooperative action by a PdAg nanocatalyst on a silica substrate whose surface is modified with amine groups. In this process, Dsub2/sub is predominantly evolved by the assist of weakly basic amine moieties, while nanocatalyst particles in the vicinity of strongly basic amine groups promote the preferential formation of HD. Kinetic data and calculations based on semi-classically corrected transition state theory coupled with density functional theory suggest that quantum tunneling dominates the hydrogen/deuterium exchange reaction over the metallic PdAg surfaces.
机译:氢同位素氘广泛应用于同位素标记的化合物和制造半导体和光纤的合成中。然而,以受控方式的氘气(D 2 )和氢氘(HD)的容纳产生是一个具有挑战性的任务,并且仍然缺乏Rational的异质催化方案。在此,我们证明了通过在用胺基改性的二氧化硅衬底上的PDAG纳米催化剂的配合作用来从甲酸和D 2 / sub> O中选择性生产氢同位素化合物。在该过程中,D 2 主要通过弱碱性胺部分的辅助来演变,而纳米催化剂颗粒在强碱胺基群附近促进了HD的优先形成。基于半经典校正过渡状态理论的动力学数据和计算与密度函数理论相结合,表明量子隧道在金属PDAG表面上占据了氢/氘交换反应。

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