National Natural Science Foundation of China(51573055,21334002,51373054)
National Basic Research Program of China(2013CB834705,2014CB643504)
and Fundamental Research Funds for the Central Universities.
This work was supported by the National Natural Science Foundation of China (51573055, 21334002, 51373054), the National Basic Research Program of China (2013CB834705, 2014CB643504), and Fundamental Research Funds for the Central Universities.
The authors declare that they have no conflict of interest.
These authors contributed equally to this work.
The supporting information is available online at
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Figure 1
CV curves for successive 40 scan cycles of poly-PDI-DUA in chloroform with TEAPF6 as supporting electrolytes and ITO as the working electrode (color online).
Scheme 1
Synthesis route of the DUA monomer, precursor polymer poly-PDI-DUA and fused polymer poly-CDI-HBC, oligomer PDI-DUA-PDI, CDI-HBC-CDI, and CDI.
Figure 2
(a) UV-Vis spectra of poly-PDI-DUA in chloroform and poly-CDI-HBC on ITO prepared by CV at a scan rate of 50 mV s−1; (b) UV-Vis spectra of CDI-HBC-CDI, CDI and PDI-DUA-PDI in chloroform at room temperature (color online).
Figure 3
Raman spectra of poly-CDI-HBC compared with poly-PDI-DUA (color online).
Figure 4
(a) Cyclicvoltammograms of the polymers poly-CDI-HBC on ITO recorded in solution at scan rate of
Figure 5