Building Supramolecular DNA-Inspired Nanowires on Gold Surfaces: From 2D to 3D

被引:13
作者
Gatto, Emanuela [1 ]
Kubitzky, Sascha [2 ]
Schriever, Marc [2 ]
Cesaroni, Simona [1 ]
Mazzuca, Claudia [1 ]
Marafon, Giulia [3 ]
Venanzi, Mariano [1 ]
De Zotti, Marta [3 ]
机构
[1] Univ Roma Tor Vergata, Dept Chem Sci & Technol, I-00133 Rome, Italy
[2] Tech Hsch Wildau, Fac Engn & Nat Sci, D-15745 Wildau, Germany
[3] Univ Padua, Dept Chem Sci, I-35131 Padua, Italy
关键词
peptides; photocurrent generation; self-assembled monolayers; self-assembly; supramolecular chemistry; SELF-ASSEMBLED MONOLAYERS; RANGE ELECTRON-TRANSFER; PHOTOCURRENT GENERATION; HELICAL PEPTIDES; PHOTOELECTROCHEMICAL PROPERTIES; PHOTOINDUCED ELECTRON; DISTANCE DEPENDENCE; ENERGY-CONVERSION; DIPOLE-MOMENT; PORPHYRIN;
D O I
10.1002/anie.201901683
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three building blocks have been designed to chemically link to a gold surface and vertically self-assemble through thymine-adenine hydrogen bonds. Starting from these building blocks, two different films were engineered on gold surface. Film1 consists of adenine linked to lipoic acid (Lipo-A) to covalently bind to the gold surface, and ZnTPP linked to a thymine (T-ZnTPP). Film2 has an additional noncovalently linked layer: a helical undecapeptide analogue of the trichoginGAIV peptide, in which four glycines were replaced by four lysines to favor a helical conformation and reduce flexibility and the two extremities were functionalized with thymine and adenine to enable Lipo-A and T-ZnTPP binding, respectively. These films were characterized by electrochemical and spectroscopic techniques, and were very stable over time and when in contact with solution. Under illumination, they could generate current with higher efficiency than similar previously described systems.
引用
收藏
页码:7308 / 7312
页数:5
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