2013
DOI: 10.1016/j.jlumin.2012.07.011
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Light emitting mechanisms in an alternated fluorene EDOT copolymer—A theoretical and photophysical study

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Cited by 7 publications
(9 citation statements)
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“…In this particular case is noteworthy that EDOT is a much stronger donor than Th and Bz, in relation to fluorene which acts as the acceptor, just the opposite of the two preceding materials. This situation was already discussed in a previous paper [13]. The UV-vis absorption spectrum in diluted CHCl 3 solution of P (FBz) exhibited two major absorption peaks around 320 and 445 nm, attributable to the p-p* transition of the main chain and to the formation of an intrachain charge transfer complex (ICT) between the donor (fluorene) and the acceptor (benzothiadiazole), respectively.…”
Section: Optical Propertiessupporting
confidence: 65%
See 1 more Smart Citation
“…In this particular case is noteworthy that EDOT is a much stronger donor than Th and Bz, in relation to fluorene which acts as the acceptor, just the opposite of the two preceding materials. This situation was already discussed in a previous paper [13]. The UV-vis absorption spectrum in diluted CHCl 3 solution of P (FBz) exhibited two major absorption peaks around 320 and 445 nm, attributable to the p-p* transition of the main chain and to the formation of an intrachain charge transfer complex (ICT) between the donor (fluorene) and the acceptor (benzothiadiazole), respectively.…”
Section: Optical Propertiessupporting
confidence: 65%
“…Bromination of 3,4-ethylenedioxythiophene with NBS gave monomer 2,5-dibromo-3,4-ethylenedioxythiophene [13] and 2,7-dibromo-9,9 0 -n-dihexylfluorene was synthesized according to a published procedure [3]. The copolymers were generated via the Suzuki polycondensation using tetrakis(triphenylphosphine) (Pd(PPh 3 ) 4 ) as a catalyst using an equimolecular mixture of the dibromide and of the diboronate.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…But the most striking feature is the high emission at 451 nm strongly red shifted in relation those of the other polymers. [46,[48][49][50] This spectral behavior is typical of aggregated structures that could be formed as a result of the absence of the bulky DBM substituents (as compared to LaPPS59Nd) and to the possibility of the Nd ion to complex with another phenanthroline unit from a neighboring chain. This would approximate the chains increasing the degree of the 𝜋-stacking, consequently red shifting the emission spectrum.…”
Section: Photophysical Propertiesmentioning
confidence: 91%
“…2,5‐Dibromo‐3,4‐ethylenedioxythiophene, 2,7‐dibromo‐9,9'‐n‐dihexylfluorene, and the alternated copolymers P(FTh), P(FEDOT), and P(FBz) were prepared according to published procedures, and the characterizations are presented in supporting information . The block copolymers P(FEDOT ‐b‐ FTh) and P(FEDOT ‐b‐ FBz) were synthesized following the procedures described below.…”
Section: Methodsmentioning
confidence: 99%