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无金属表面光化学末端炔烃同偶联反应。

Metal-Free on-Surface Photochemical Homocoupling of Terminal Alkynes.

机构信息

Dipartimento di Scienze Chimiche, Università di Padova , Via Marzolo 1, 35131 Padova, Italy.

CNR-ICMATE, Via Marzolo 1, 35131 Padova, Italy.

出版信息

J Am Chem Soc. 2016 Aug 17;138(32):10151-6. doi: 10.1021/jacs.6b03589. Epub 2016 Aug 4.

Abstract

On-surface synthesis involving the homocoupling of aryl-alkynes affords the buildup of bisacetylene derivatives directly at surfaces, which in turn may be further used as ingredients for the production of novel functional materials. Generally, homocoupling of terminal alkynes takes place by thermal activation of molecular precursors on metal surfaces. However, the interaction of alkynes with surface metal atoms often induces unwanted reaction pathways when thermal energy is provided to the system. In this contribution we report about light-induced metal-free homocoupling of terminal alkynes on highly oriented pyrolitic graphite (HOPG). The reaction occurred with high efficiency and selectivity within a self-assembled monolayer (SAM) of aryl-alkynes and led to the generation of large domains of ordered butadiynyl derivatives. Such a photochemical uncatalyzed pathway represents an original approach in the field of topological C-C coupling at the solid/liquid interface.

摘要

表面合成涉及芳基-炔烃的同偶联,可直接在表面构建双乙炔衍生物,进而可进一步用作新型功能材料的原料。通常,末端炔烃的同偶联是通过金属表面上分子前体的热激活来实现的。然而,当向体系提供热能时,炔与表面金属原子的相互作用往往会导致不希望的反应途径。在本研究中,我们报道了在高取向热解石墨(HOPG)上用光诱导无金属末端炔烃的同偶联。该反应在芳基-炔烃的自组装单层(SAM)中具有高效率和选择性,导致有序丁二炔基衍生物的大片域生成。这种光化学无催化剂途径代表了固/液界面拓扑 C-C 偶联领域的一种原始方法。

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