Transformation of Self-Assembled Structure by the Addition of Active Reactant

被引:28
作者
Li, Yibao [2 ]
Wan, Junhua [3 ]
Deng, Ke [2 ]
Han, Xiaona [1 ]
Lei, Shengbin [4 ,5 ]
Yang, Yanlian [2 ]
Zheng, Qiyu [1 ]
Zeng, Qingdao [2 ]
Wang, Chen [2 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[2] Natl Ctr Nanosci & Technol, Beijing 100190, Peoples R China
[3] Hangzhou Normal Univ, Minist Educ, Key Lab Organosilicon Chem & Mat Technol, Hangzhou 310012, Zhejiang, Peoples R China
[4] Harbin Inst Technol, Minist Educ, Key Lab Microsyst & Microstruct Mfg, Harbin 150080, Peoples R China
[5] Harbin Inst Technol, Acad Fundamental & Interdisciplinary Sci, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
2-DIMENSIONAL MOLECULAR NETWORK; SUPRAMOLECULAR NETWORKS; TRIMESIC ACID; ISOMERIZATION; ARCHITECTURES; DERIVATIVES; FABRICATION; ADSORPTION; STM;
D O I
10.1021/jp1097876
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
We have designed and synthesized one molecular building block, an aromatic trialdehyde derivative with three aldehyde groups, to form a potentially active structure. The scanning tunneling microscopy (STM) images show that the trialdehyde derivative forms lamellar structures. By the addition of active reactant, 5-aminoisophthalic acid, it is found that the structure of the adlayer can be transformed from lamellar to hexagonal structure as was expected. The structural formation of molecular networks is attributed to the condensation reaction between aldehyde and amine. Density functional theory (DFT) calculations reveal the observation of structural transformation at the solid/liquid interface due to the more stable adsorption of the triimine product than that of the trialdehyde derivative.
引用
收藏
页码:6540 / 6544
页数:5
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