Aggregation of One-Dimensional Wires: The Case of Long Oligoynes

被引:0
|
作者
Gordillo-Gamez, Fernando [1 ]
Gao, Yueze [2 ]
Arago, Juan [3 ]
Orti, Enrique [3 ]
Aranda, Daniel [3 ]
Kertesz, Miklos [4 ,5 ]
Tykwinski, Rik R. [2 ]
Casado, Juan [1 ]
机构
[1] Univ Malaga, Dept Phys Chem, Andalucia Tech Campus Teatinos S N, E-29071 Malaga, Spain
[2] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
[3] Univ Valencia, Inst Ciencia Mol ICMol, Paterna 46980, Spain
[4] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
[5] Georgetown Univ, Inst Soft Matter, Washington, DC 20057 USA
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
one-dimensional wires; oligoynes; aggregation; H-type aggregates; SPECTRAL SIGNATURES; CARBON;
D O I
10.1002/anie.202404014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We show an unexpected aggregation phenomenon of a long oligoyne (Py[16]) with 16 contiguous triple bonds and endcapped with bulky 3,5-bi(3,5-bis-tert-butylphenyl)pyridine groups. Aggregation of 1D pi-conjugated oligoyne chains is rare given the minimal pi-pi intermolecular interactions as well as its flexibility that works against self-assembly. In dilute solutions, the reversible aggregation of Py[16] initiates at low temperature in the range of 140-180 K, and is not observed for shorter oligoynes in this series. Cryogenic UV/Vis electronic absorption spectra and vibrational Raman spectra with different laser wavelength lines tuning from in-resonance to off-resonance conditions have been used to extract the vibrational features characterizing the monomer and aggregate species. Theoretical calculations complement the spectroscopic findings. The reversible aggregation of an oligoyne with 16 triple bonds is described. The association phenomenon occurs in spite of the flexibility and the minimal pi surface of the oligoyne. image
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页数:5
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