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Solvent-Dependent Core-Modified Rubyrin Self-Assembly at Liquid/Solid Interfaces

delete2020-03-26
delete16
PRE
AI
陈
陈晨 (Chen Chen)
张思琪 封面图
张思琪 (Siqi Zhang)
涂斌 封面图
涂斌 (Bin Tu)
T
Ting Meng
J
Jianqiao Li
Y
Yuxin Qian
P
Pengfei Li
B
Bo Liu
W
Wubiao Duan *
徐海军 封面图
徐海军 (Haijun Xu) *
F
Fengying Zhao *
杨
杨鹏 (Peng Yang)
李
李晶 (Jing Li)
Q
Qingdao Zeng *
DOI:10.1021/acs.langmuir.9b03867delete
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摘要

摘要

En 中文
Scanning tunneling microscopy (STM) was utilized to disclose four novel core-modified rubyrin self-assembly behaviors on the highly-oriented pyrolytic graphite (HOPG) surface, of which N2S4-OR(1)/N2Se4-OR(2) had no phenanthrene pyrrole ring and N2S4-OR(3)/N2Se4-OR(4) had phenanthrene-fused pyrrole rings and meso-aryl substituents. It was discovered that the core-modified rubyrin could self-assemble into either face-on or edge-on monolayer structures selectively at the liquid/HOPG interface in different solvents. There was an obvious solventdependent self-assembly for N2S4-OR(3)/N2Se4-OR(4), which adopted an edge-on and face-on structure in 1-phenyloctane and 1-heptanoic acid solvents, respectively, whereas N2S4-OR(1)/ N2Se4-OR(2) showed no obvious difference in the assembly structure, which both adopted a face-on structure in the two solvents. Density functional theory (DFT) calculations were also utilized to reveal the relevant self-assembly mechanisms. This study shows a typical solvent effect regulating core-modified rubyrin self-assembly, which is essential for porphyrin-based functional devices' design and manufacture.
Keyword:
SUPRAMOLECULAR CHEMISTRY
PORPHYRIN
COORDINATION
SUBSTITUENTS
NETWORKS
RINGS
STM
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期刊

Langmuir 封面图
Langmuir
IF:
3.9
论文数:
5.4W
被引数:
10.6W

机构

B
Beijing Jiaotong University
学者数:
2.2W
论文数: 1.7W
被引数: 1.2W
J
jiangxi college of applied technology
学者数:
95
论文数: 84
被引数: 0
N
Nanjing Forestry University
学者数:
2.0W
论文数: 1.6W
被引数: 3.2W
C
chinese academy of sciences
学者数:
56.7W
论文数: 45.0W
被引数: 704
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