2015
DOI: 10.1016/j.jelechem.2015.05.028
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The effect of the different donor units on fluorescent conjugated polymers containing 2,1,3-benzooxadiazole as the acceptor unit

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Cited by 20 publications
(5 citation statements)
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“…1,2-Bis (octyloxy)benzene, 1,2-dinitro-4,5-bis(octyloxy)benzene, 5,6-bis (octyloxy)benzo[c] [1,2,5]oxadiazole, 4,7-dibromo-5,6-bis(octyloxy) benzo[c] [1,2,5]oxadiazole, tributyl(thiophene-2-yl)stannane and 5,6bis(octyloxy)-4,7-di(thiophen-2-yl)benzo[c] [1,2,5]oxadiazole (M1) were synthesized according to previously described methods. [60][61][62][63] Four monomers; M1, M2, M3 and M4 were brominated using N-bromosuccinimide in chloroform solution using acetic acid as the catalyst (Scheme 1). All reactions were carried out under inert atmosphere unless otherwise mentioned.…”
Section: Methodsmentioning
confidence: 99%
“…1,2-Bis (octyloxy)benzene, 1,2-dinitro-4,5-bis(octyloxy)benzene, 5,6-bis (octyloxy)benzo[c] [1,2,5]oxadiazole, 4,7-dibromo-5,6-bis(octyloxy) benzo[c] [1,2,5]oxadiazole, tributyl(thiophene-2-yl)stannane and 5,6bis(octyloxy)-4,7-di(thiophen-2-yl)benzo[c] [1,2,5]oxadiazole (M1) were synthesized according to previously described methods. [60][61][62][63] Four monomers; M1, M2, M3 and M4 were brominated using N-bromosuccinimide in chloroform solution using acetic acid as the catalyst (Scheme 1). All reactions were carried out under inert atmosphere unless otherwise mentioned.…”
Section: Methodsmentioning
confidence: 99%
“…The replacement of the selenium atom with the sulfur atom allows to adjust the absorption spectra and bandgaps of the conjugated polymers due to the large diameter of the selenium atom and its lower electronegativity. 12 In addition, the better polarizability of selenium atom than sulfur atom provides selenium-based polymers greater charge mobility and transfer. In addition, the ability to substitute the alkyl chain at the fifth and sixth positions in the benzazole group results in readily soluble polymers.…”
Section: Introductionmentioning
confidence: 99%
“…Due to these features, the thieno[3,2- b ]thiophene group was chosen as the electron donor and the 2,1,3-benzoselenadiazole group was the electron acceptor group in the synthesis of the donor–acceptor type low bandgap polymer preferred in this work. 12…”
Section: Introductionmentioning
confidence: 99%
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“…These desirable properties have prompted much interest in selenophene containing polymers for both organic solar cell and transistor applications [12]. In literature, there are several examples for selenophene containing conjugated polymers which have been reported with improved device performance, especially charge carrier mobility, over their thiophene-containing analogues [13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%