Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS), Departamento de Química Orgánica, Universidade de Santiago de Compostela, 15782-, Santiago de Compostela, Spain.
IBM Research-Zurich, 8803, Rüschlikon, Switzerland.
Angew Chem Int Ed Engl. 2021 Dec 6;60(50):26346-26350. doi: 10.1002/anie.202110311. Epub 2021 Nov 10.
The Diels-Alder reaction is one of the most popular reactions in organic chemistry. However, its use in the field of on-surface synthesis is hampered by the spatial restrictions of this cycloaddition reaction. Herein we selected a cyclic strained triyne to demonstrate an on-surface hexadehydro-Diels-Alder reaction in a single molecule. The reaction was studied in detail by means of atomic force microscopy (AFM) with CO-functionalized tips. Our results pave the way to use this iconic pericyclic reaction for on-surface synthesis, introducing the concept of atom economy in the field.
Diels-Alder 反应是有机化学中最受欢迎的反应之一。然而,其在表面合成领域的应用受到这种环加成反应空间限制的阻碍。在此,我们选择了一种环状张力三炔来在单个分子中展示表面合成中的十六氢化 Diels-Alder 反应。原子力显微镜 (AFM) 结合 CO 功能化针尖对反应进行了详细研究。我们的结果为在表面合成中使用这种标志性的周环反应铺平了道路,为该领域引入了原子经济性的概念。