Premium
Direct Formation of C−C Triple‐Bonded Structural Motifs by On‐Surface Dehalogenative Homocouplings of Tribromomethyl‐Substituted Arenes
Author(s) -
Sun Qiang,
Yu Xin,
Bao Meiling,
Liu Mengxi,
Pan Jinliang,
Zha Zeqi,
Cai Liangliang,
Ma Honghong,
Yuan Chunxue,
Qiu Xiaohui,
Xu Wei
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201801056
Subject(s) - graphyne , carbyne , moiety , scanning tunneling microscope , alkyl , triple bond , chemistry , nanostructure , dimer , materials science , carbon fibers , nanotechnology , density functional theory , crystallography , stereochemistry , graphene , composite number , computational chemistry , polymer chemistry , double bond , organic chemistry , catalysis , carbene , composite material
On‐surface synthesis shows significant potential in constructing novel nanostructures/nanomaterials, which has been intensely studied in recent years. The formation of acetylenic scaffolds provides an important route to the fabrication of emerging carbon nanostructures, including carbyne, graphyne, and graphdiyne, which feature chemically vulnerable sp‐hybridized carbon atoms. Herein, we designed and synthesized a tribromomethyl‐substituted compound. By using a combination of high‐resolution scanning tunneling microscopy, non‐contact atomic force microscopy, and density functional theory calculations, we demonstrated that it is feasible to convert these compounds directly into C−C triple‐bonded structural motifs by on‐surface dehalogenative homocoupling reactions. Concurrently, sp 3 ‐hybridized carbon atoms are converted into sp‐hybridized ones, that is, an alkyl group is transformed into an alkynyl moiety. Moreover, we achieved the formation of dimer structures, one‐dimensional molecular wires, and two‐dimensional molecular networks on Au(111) surfaces, which should inspire further studies towards two‐dimensional graphyne structures.