论文标题

在AU上环化后的非共价二聚化(111)

Non-Covalent Dimerization after Enediyne Cyclization on Au(111)

论文作者

de Oteyza, Dimas G., Paz, Alejandro Pérez, Chen, Yen-Chia, Pedramrazi, Zahra, Riss, Alexander, Wickenburg, Sebastian, Tsai, Hsin-Zon, Fischer, Felix R., Crommie, Michael F., Rubio, Angel

论文摘要

我们使用扫描隧道显微镜和计算机模拟研究了AU(111)上1,2 -Bis(2-苯基乙基)苯的热诱导的环化。已知众所周知,在溶液中的两种竞争机制:经典的C1 -C6或C1 -C1 -C5环化途径中进行环化。在AU(111)上,我们发现C1 -C5环化被抑制,并且C1 -C6环化产生了高度紧张的双环烯烃,其表面化学迄今未知。 C1-C6产物自组装成表面上的非共价二聚体。根据密度功能理论计算,讨论了非共价关联​​背后的反应机制和驱动力。

We investigate the thermally-induced cyclization of 1,2 - bis(2 - phenylethynyl)benzene on Au(111) using scanning tunneling microscopy and computer simulations. Cyclization of sterically hindered enediynes is known to proceed via two competing mechanisms in solution: a classic C1 - C6 or a C1 - C5 cyclization pathway. On Au(111) we find that the C1 - C5 cyclization is suppressed and that the C1 - C6 cyclization yields a highly strained bicyclic olefin whose surface chemistry was hitherto unknown. The C1 - C6 product self-assembles into discrete non-covalently bound dimers on the surface. The reaction mechanism and driving forces behind non-covalent association are discussed in light of density functional theory calculations.

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