Ladder Phenylenes Synthesized on Au(111) Surface via Selective [2+2] Cycloaddition

• Published in: Journal of the American Chemical Society Vol. 143; no. 33; pp. 12955 - 12960
• Main Authors: Li, Deng-Yuan, Qiu, Xia, Li, Shi-Wen, Ren, Yin-Ti, Zhu, Ya-Cheng, Shu, Chen-Hui, Hou, Xiao-Yu, Liu, Mengxi, Shi, Xing-Qiang, Qiu, Xiaohui, Liu, Pei-Nian
• Format: Journal Article
• Language: English
• Published: American Chemical Society 25.08.2021
• Subjects: atomic force microscopy; benzene; chemoselectivity; cycloaddition reactions; density functional theory; polymers; spectroscopy
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.1c05586

Ladder phenylenes (LPs) composed of alternating fused benzene and cyclobutadiene rings have been synthesized in solution with a maximum length no longer than five units. Longer polymeric LPs have not been obtained so far because of their poor stability and insolubility. Here, we report the synthesis of linear LP chains on the Au(111) surface via dehalogenative [2+2] cycloaddition, in which the steric hindrance of the methyl groups in the 1,2,4,5-tetrabromo-3,6-dimethylbenzene precursor improves the chemoselectivity as well as the orientation orderliness. By combining scanning tunneling microscopy and noncontact atomic force microscopy, we determined the atomic structure and the electronic properties of the LP chains on the metallic substrate and NaCl/Au(111). The tunneling spectroscopy measurements revealed the charged state of chains on the NaCl layer, and this finding is supported by density functional theory calculations, which predict an indirect bandgap and antiferromagnetism in the polymeric LP chains.