Synthesis of Dendronized Polymers on the Au(111) Surface

被引:2
|
作者
Zhu, Ya-Cheng [1 ]
Xue, Fu-Hua [1 ]
Kang, Li-Xia [1 ]
Liu, Jian-Wei [1 ]
Wang, Ying [1 ]
Li, Deng-Yuan [1 ]
Liu, Pei-Nian [1 ]
机构
[1] East China Univ Sci & Technol, Frontiers Sci Ctr Materiobiol & Dynam Chem, Sch Chem & Mol Engn,Key Lab Adv Mat, Shanghai Key Lab Funct Mat Chem,State Key Lab Chem, Shanghai 200237, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2022年 / 13卷 / 45期
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
GRAPHENE NANORIBBONS; JACKETED POLYMERS; POLYMERIZATION; DENDRIMERS; CARBAZOLE; MAGNETISM; ELECTRON;
D O I
10.1021/acs.jpclett.2c02810
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dendronized polymers (DPs) consist of a linear polymeric backbone with dendritic side chains. Fine-tuning of the functional groups in the side chains enriches the structural versatility of the DPs and imparts a variety of novel physical properties. Herein, the first on-surface synthesis of DPs is achieved via the postfunctionalization of polymers on Au(111), in which the surface-confinement-induced planar conformation and chiral configurations were unambiguously characterized. While the dendronized monomer was synthesized in situ on Au(111), the subsequent polymerization afforded only short, cross-linked DP chains owing to multiple side reactions. The postfunctionalization approach selectively produced brominated polyphenylene backbone moieties by the deiodination polymerization of 4-bromo-4 ''- iodo-5 '-(4-iodophenyl)-1,1 ':3 ',1 ''-terphenyl on Au(111), which smoothly underwent divergent cross-coupling reactions with two different isocyanides to form two types of DPs as individual long chains.
引用
收藏
页码:10589 / 10596
页数:8
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