Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/95458
Title: Electrochromic π-Conjugated Copolymers Derived from Azulene, Fluorene, and Dialkyloxybenzothiadiazole
Authors: Lim, S.Z.H.
Neo, W.T.
Cho, C.M.
Wang, X.
Tan, A.Y.X.
Chan, H.S.O. 
Xu, J.
Issue Date: 2013
Citation: Lim, S.Z.H., Neo, W.T., Cho, C.M., Wang, X., Tan, A.Y.X., Chan, H.S.O., Xu, J. (2013). Electrochromic π-Conjugated Copolymers Derived from Azulene, Fluorene, and Dialkyloxybenzothiadiazole. Australian Journal of Chemistry 66 (9) : 1048-1056. ScholarBank@NUS Repository.
Abstract: A series of random π-conjugated copolymers P1, P2, and P3 were synthesised from 1,3-dibromoazulene, 4,7-dibromo-5,6-bis(dodecyloxy)benzo-2,1,3- thiadiazole, and 9,9-dioctylfluorene-2,7-bis(trimethyleneborate) via Suzuki coupling reactions. The copolymers P1-3 had molecular weights in the range of 17000-30900gmol-1 with polydispersity indexes of 1.45-2.03. Thermal analysis showed that the polymers P1-3 had good thermal stability with decomposition temperatures ranging from 341-363°C both in air and in nitrogen. Photoluminescence studies showed that polymer P1 and P2 are weakly fluorescent with low quantum yields of 0.013 and 0.0029 for P1 borne with 30% azulene and P2 borne with 50% azulene in the polymer backbone, respectively. P3 borne with 70% azulene resulted in complete quenching of fluorescence. The electrochemical band gaps for P1-3 are very close to their corresponding optical band gaps. Electrochromic study showed that three polymer thin films displayed the same colour change from yellowish green at the neutral and electrochemically-reduced state to greyish brown at the electrochemically-oxidised state. In particular, electrochromic contrasts of 17% and 13% for P2 and P3, respectively, were recorded in the near infrared region. © 2013 CSIRO.
Source Title: Australian Journal of Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/95458
ISSN: 00049425
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