Templated Synthesis of End-Functionalized Graphene Nanoribbons through Living Ring-Opening Alkyne Metathesis Polymerization

• Published in: Journal of the American Chemical Society Vol. 141; no. 28; pp. 11050 - 11058
• Main Authors: von Kugelgen, Stephen, Piskun, Ilya, Griffin, James H, Eckdahl, Christopher T, Jarenwattananon, Nanette N, Fischer, Felix R
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 17.07.2019; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Multidisciplinary; Physical Sciences; Science & Technology; POLYMERS; ROMP; BAND-GAP
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.9b01805

Atomically precise bottom-up synthesized graphene nanoribbons (GNRs) are promising candidates for next-generation electronic materials. The incorporation of these highly tunable semiconductors into complex device architectures requires the development of synthetic tools that provide control over the absolute length, the sequence, and the end groups of GNRs. Here, we report the living chain-growth synthesis of chevron-type GNRs (cGNRs) templated by a poly-(arylene ethynylene) precursor prepared through ring-opening alkyne metathesis polymerization (ROAMP). The strained triple bonds of a macrocyclic monomer serve both as the site of polymerization and the reaction center for an annulation reaction that laterally extends the conjugated backbone to give cGNRs with predetermined lengths and end groups. The structural control provided by a living polymer-templated synthesis of GNRs paves the way for their future integration into hierarchical assemblies, sequence-defined heterojunctions, and well-defined single-GNR transistors via block copolymer templates.