@article{oai:oist.repo.nii.ac.jp:02000315,
 author = {Yao, Xuelin and Zhang, Heng and Kong, Fanmiao and Hinaut, Antoine and Pawlak, Rémy and Okuno, Masanari and Graf, Robert and Horton, Peter N. and Coles, Simon J. and Meyer, Ernst and Bogani, Lapo and Bonn, Mischa and Wang, Hai I. and Müllen, Klaus and Narita, Akimitsu},
 issue = {46},
 journal = {Angewandte Chemie International Edition},
 month = {Oct},
 note = {Structurally defined graphene nanoribbons (GNRs) have emerged as promising candidates for nanoelectronic devices. Low band gap (<1 eV) GNRs are particularly important when considering the Schottky barrier in device performance. Here, we demonstrate the first solution synthesis of 8-AGNRs through a carefully designed arylated polynaphthalene precursor. The efficiency of the oxidative cyclodehydrogenation of the tailor-made polymer precursor into 8-AGNRs was validated by FT-IR, Raman, and UV/Vis-near-infrared (NIR) absorption spectroscopy, and further supported by the synthesis of naphtho[1,2,3,4-ghi]perylene derivatives (1 and 2) as subunits of 8-AGNR, with a width of 0.86 nm as suggested by the X-ray single crystal analysis. Low-temperature scanning tunneling microscopy (STM) and solid-state NMR analyses provided further structural support for 8-AGNR. The resulting 8-AGNR exhibited a remarkable NIR absorption extending up to ∼2400 nm, corresponding to an optical band gap as low as ∼0.52 eV. Moreover, optical-pump TeraHertz-probe spectroscopy revealed charge-carrier mobility in the dc limit of ∼270 cm2 V−1 s−1 for the 8-AGNR.},
 title = {N=8 Armchair Graphene Nanoribbons: Solution Synthesis and High Charge Carrier Mobility},
 volume = {62},
 year = {2023}
}