Abstract
This paper reports the self-assembly of two new tetrathiafulvalene (TTF) derivatives that contain one or two urethane groups. The formation of nanoribbons was evidenced by scanning electron microscopy (SEM) and X-ray diffraction (XRD), which showed that the self-assembly ability of T1 was better than that of T2. The results revealed that more urethane groups in a molecule did not necessarily instigate self-assembly. UV-vis and FTIR spectra were measured to explore noncovalent interactions. The driving forces for self-assembly of TTF derivatives were mainly hydrogen bond interactions and π-π stacking interactions. The electronic conductivity of the T1 and T2 films was tested by a four-probe method.
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Sun, X., Lai, G., Li, Z., Ma, Y., Yuan, X., Shen, Y., & Wang, C. (2015). Urethane tetrathiafulvalene derivatives: Synthesis, self-assembly and electrochemical properties. Beilstein Journal of Organic Chemistry, 11, 2343–2349. https://doi.org/10.3762/bjoc.11.255
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