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• W3175291272 endingPage "150529" @default.
• W3175291272 startingPage "150529" @default.
• W3175291272 abstract "Crystallization behaviors of 1,3,5-tri(1H-benzo[d]imidazol-2-yl) benzene (BTIB), gallic acid derivative (A10), and their hydrogen-bonded complex BTIB/A10 on Highly Oriented Graphite(HOPG) surface were studied by scanning tunneling microscope (STM) in combination with density functional theory (DFT) calculations. Single component BTIB self-assembled into porous and linear nanostructures, and A10 aggregated into linear nanostructure. Induced by the intermolecular interactions, an ordered BTIB/A10 nanostructure with the molecular ratio of 1:3 was in situ obtained and identical to the bulk assembly structure. When 1,3,5-Tris(4-carboxyphenylethynyl) benzene (H3BTE) or 1,3,5-tris(10-carboxydecyloxy)-benzene (TCDB) instead of A10 was adopted, porous nanostructure with the molar ratio of 1:1 was in situ prepared in BTIB/H3BTE and BTIB/TCDB system respectively, which indicated the regulatory effect of the number of aromatic acids’ carboxyl groups on the co-assemblies of BTIB and aromatic acids. Simultaneously, the flexible connection groups between the three carboxyl groups and the central benzene ring in TCDB resulted in the formation of another co-assembly nanostructure in BTIB/TCDB system, which was different from the BTIB/H3BTE system. These results would be contributed to deepening the understanding of the interfacial crystal behaviors and probably providing an efficient pathway of regulating the structures of binary hydrogen-bonded crystals." @default.
• W3175291272 created "2021-07-05" @default.
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• W3175291272 date "2021-11-01" @default.
• W3175291272 modified "2023-10-01" @default.
• W3175291272 title "Programmable binary crystallization behaviors assisted by hydrogen bond on HOPG surface" @default.
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• W3175291272 doi "https://doi.org/10.1016/j.apsusc.2021.150529" @default.
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