2010
DOI: 10.1002/pola.23972
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Conjugated polymers atypically prepared in water

Abstract: Processability remains a fundamental issue for the implementation of conducting polymer technology. A simple synthetic route towards processable precursors to conducting polymers (main chain and side chain) was developed using commercially available materials. These soluble precursor systems were converted to conjugated polymers electrochemically in aqueous media, offering a cheaper and greener method of processing. Oxidative conversion in aqueous and organic media each produced equivalent electrochromics. The… Show more

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Cited by 6 publications
(6 citation statements)
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“…To date, PEDOT/PSS has been the most successfully commercialized polythiophene. Based on it, conducting polymers enclosed PEDOT attract more and more attention because of their wide commercial applications,6–11 for example, as antistatic coating materials, as transparent anodes and buffer layers in OSCs, as hole‐injection layers in OLEDs, as electrodes, and active layers in OFETs 2. In the past twenty years, vast amount of work has been carried out on the design and polymerization of EDOT analogs with novel structure and the properties of the resulting polymers 2, 3…”
Section: Introductionmentioning
confidence: 99%
“…To date, PEDOT/PSS has been the most successfully commercialized polythiophene. Based on it, conducting polymers enclosed PEDOT attract more and more attention because of their wide commercial applications,6–11 for example, as antistatic coating materials, as transparent anodes and buffer layers in OSCs, as hole‐injection layers in OLEDs, as electrodes, and active layers in OFETs 2. In the past twenty years, vast amount of work has been carried out on the design and polymerization of EDOT analogs with novel structure and the properties of the resulting polymers 2, 3…”
Section: Introductionmentioning
confidence: 99%
“…2,3,5 To date, PEDOT/PSS has been the most successfully commercialized polythiophene. Based on it, conducting polymers enclosed PEDOT attract more and more attention because of their wide commercial applications, [6][7][8][9][10][11] for example, as antistatic coating materials, as transparent anodes and buffer layers in OSCs, as hole-injection layers in OLEDs, as electrodes, and active layers in OFETs. 2 In the past twenty years, vast amount of work has been carried out on the design and polymerization of EDOT analogs with novel structure and the properties of the resulting polymers.…”
mentioning
confidence: 99%
“…2,3 (BDOT); 12,13 (2) sulfur analogs, 3,4-methylenedithiathiophene (MDTT), 3,4-ethylenedithiathiophene (EDTT), EDTT-R (R ¼ Br, CH 2 OH etc. ), 3,4-propylenedithiathiophene (PDTT), and thieno [3,4-b]-1,4-oxathiane (EOTT); [14][15][16][17][18] (3) selenium analogs, 3,4-ethylenedioxyselenophene (EDOS), 3,4-propylenedioxyselenophene (PDOS), PEDOS-R 2 (R 2 ¼ C n H 2nþ1 , n ¼ 4, 6, 10), 3,4ethylenedithioselenophene (EDTS), seleno [3,4-b]-1,4-oxathiane (EOTS), and 3,4-ethylenediselenathiophene (EDST); [19][20][21][22][23][24][25] (4) nitrous analogs, 3,4-methylenedioxypyrrole (MDOPy), 3,4-ethylenedioxypyrrole (EDOPy), 3,4-propylenedioxypyrrole (PDOPy), 3,4-butylenedioxypyrrole (BDOPy), 3,4-methylenedithiopyrrole (MDTPy), and 3,4-ethylenedithiopyrrole (EDTPy); [26][27][28][29] (5) phosphorous analog, 3,4-ethylenedithiaphosphole (EDPP); 30 (6) oxygenic analogs, 3,4-ethylendithiafurane (EDTF), 3,4-ethylenedioxyfuran (EDOF), and 3,4-dihydro-2H-thieno [3,4-b]pyran (EDTP); [31][32][33] (7) telluric analog, 3,4-ethylenedioxytellurophene (EDOTe) as a predicted structure based on 3,4dimethoxytellurophene (DMOTe). 34 Structures of the above are summarized in Scheme 2.…”
mentioning
confidence: 99%
“…Afterwards, dibromo- or diiodoEDOT is added and a Ni(II) catalyst promotes the coupling to give terEDOT [ 54 , 55 , 56 , 57 , 58 , 59 ]. Kumada reaction was also applied to the synthesis of other unsubstituted EDOT-based trimers, such as thiophene-EDOT-thiophene [ 60 , 61 ] or EDOT-Thiophene-EDOT [ 62 , 63 ]. In alternative, Suzuki [ 64 , 65 , 66 ] and Stille [ 67 , 68 , 69 , 70 ] coupling reactions offer valuable routes for the synthesis of EDOT-based trimers.…”
Section: Trimer Structuresmentioning
confidence: 99%
“… Examples of ether-substituted trimers. ( I ) [ 288 ]; ( II ) [ 281 ]; ( III ) [ 305 ]; ( IV ) [ 62 ]. …”
Section: Figures and Schemesmentioning
confidence: 99%