BNLMS, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Molecules. 2020 Aug 19;25(17):3766. doi: 10.3390/molecules25173766.
The on-surface C-H bond activation and coupling reaction is a powerful approach to constructing fine-tuned surface nanostructures. It is quite challenging to control its regioselectivity due to the inertness of the C-H bond involved. With scanning tunneling microscopy/spectroscopy and theoretical calculations, the C-H activation and sequential intramolecular dehydrocyclization of -tetra(p-methoxyphenyl)porphyrinatocobalt(II) was explored on Au(111), showing that the methoxy groups in the molecule could kinetically mediate the selectivity of the intramolecular reaction over its intermolecular coupling counterpart. The experimental results demonstrate that the introduced protecting group could help augment the selectivity of such on-surface reaction, which can be applied to the precise fabrication of functional surface nanostructures.
表面 C-H 键的活化和偶联反应是构建精细表面纳米结构的一种有力方法。由于涉及的 C-H 键的惰性,要控制其区域选择性是极具挑战性的。通过扫描隧道显微镜/光谱和理论计算,研究了 -四(对甲氧基苯基)卟啉钴(II)在 Au(111)表面上的 C-H 活化和顺序分子内脱氢环化反应,结果表明,分子中的甲氧基基团可以在动力学上调节分子内反应的选择性,使其优于其分子间偶联反应。实验结果表明,引入保护基团有助于提高这种表面反应的选择性,这可应用于功能表面纳米结构的精确制造。