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原子力显微镜诱导芳炔的表面生成与成像。

On-surface generation and imaging of arynes by atomic force microscopy.

机构信息

IBM Research-Zurich, 8803 Rüschlikon, Switzerland.

Centro de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS) and Departamento de Química Orgánica, Universidade de Santiago de Compostela. Santiago de Compostela 15782, Spain.

出版信息

Nat Chem. 2015 Aug;7(8):623-8. doi: 10.1038/nchem.2300. Epub 2015 Jul 13.

Abstract

Reactive intermediates are involved in many chemical transformations. However, their characterization is a great challenge because of their short lifetimes and high reactivities. Arynes, formally derived from arenes by the removal of two hydrogen atoms from adjacent carbon atoms, are prominent reactive intermediates that have been hypothesized for more than a century. Their rich chemistry enables a widespread use in synthetic chemistry, as they are advantageous building blocks for the construction of polycyclic compounds that contain aromatic rings. Here, we demonstrate the generation and characterization of individual polycyclic aryne molecules on an ultrathin insulating film by means of low-temperature scanning tunnelling microscopy and atomic force microscopy. Bond-order analysis suggests that a cumulene resonance structure is the dominant one, and the aryne reactivity is preserved at cryogenic temperatures. Our results provide important insights into the chemistry of these elusive intermediates and their potential application in the field of on-surface synthesis.

摘要

反应中间体参与了许多化学反应。然而,由于它们的寿命短、反应活性高,因此对其进行特征描述是一个巨大的挑战。芳炔,是通过从相邻碳原子上除去两个氢原子而从芳烃衍生而来的,是一个多世纪以来被假设存在的重要反应中间体。它们丰富的化学反应性使它们在合成化学中得到广泛应用,因为它们是构建含有芳香环的多环化合物的有利构建块。在这里,我们通过低温扫描隧道显微镜和原子力显微镜在超薄绝缘膜上演示了单个多环芳炔分子的生成和特征描述。键级分析表明,累积双键共振结构是主要的结构,并且芳炔的反应活性在低温下得以保留。我们的结果为这些难以捉摸的中间体的化学性质及其在表面合成领域的潜在应用提供了重要的见解。

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