Real-Space Imaging of a Single-Molecule Monoradical Reaction.
Shaotang SongNa GuoXinzhe LiGuangwu LiYohei HaketaMykola TelychkoJie SuPin LyuZhizhan QiuHanyan FangXinnan PengJing LiXinbang WuYing LiChenliang SuMing Joo KohJishan WuHiromitsu MaedaChun ZhangJiong LuPublished in: Journal of the American Chemical Society (2020)
Organic radicals consisting of light elements exhibit a low spin-orbit coupling and weak hyperfine interactions with a long spin coherence length, which are crucial for future applications in molecular spintronics. However, the synthesis and characterization of these organic radicals have been a formidable challenge due to their chemical instability arising from unpaired electrons. Here, we report a direct imaging of the surface chemical transformation of an organic monoradical synthesized via the monodehydrogenation of a chemically designed precursor. Bond-resolved scanning tunneling microscopy unambiguously resolves various products formed through a complex structural dissociation and rearrangement of organic monoradicals. Density functional theory calculations reveal detailed reaction pathways from the monoradical to different cyclized products. Our study provides unprecedented insights into complex surface reaction mechanisms of organic radical reactions at the single molecule level, which may guide the design of stable organic radicals for future quantum technology applications.