Simultaneous construction of two linkages for the on-surface synthesis of imine-boroxine hybrid covalent organic frameworks.
Simultaneous construction of two linkages for the on-surface synthesis of imine-boroxine hybrid covalent organic frameworks.
复制标题
同时构建两个键用于亚胺-环硼氧烷杂化共价有机框架的表面合成
DOI:
10.1039/c6sc03590f
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发表时间:
2017-03-01
期刊:
影响因子:
8.4
通讯作者:
Wang D
中科院分区:
文献类型:
--
作者:
Yue JY;Mo YP;Li SY;Dong WL;Chen T;Wang D
The orthogonality between the Schiff base reaction and the boronic acid dehydration reaction is explored during the on-surface synthesis process. The orthogonality between the Schiff base reaction and the boronic acid dehydration reaction is explored during the on-surface synthesis process. By activating the above two reactions in one-step and employing asymmetrical substituted monomers and the 3-fold symmetric monomer 1,3,5-tris(4-aminophenyl)benzene (TAPB), highly ordered imine–boroxine hybrid single-layered covalent organic frameworks (sCOFs) have been successfully constructed on HOPG by a gas–solid interface reaction method and characterized by scanning tunnelling microscopy (STM). In particular, the reaction between the meta-substituted monomer and TAPB generates sCOFB with a windmill structure, which is the first sCOF with surface chirality so far reported. The demonstration of the one-step synthesis of multiple linkages to form sCOFs can further enlarge the sCOF family and expand the design routes for functional 2D organic nanomaterials.