2011
DOI: 10.1039/c0jm02679d
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Tuning of electronic properties and rigidity in PEDOT analogs

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Cited by 58 publications
(80 citation statements)
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“…70%). In comparison with other routes,15, 16, 22, 35, 51–54 this transetherification reaction can avoid complex operating procedures and strict reaction conditions. More importantly, by modifying the raw material quantity, reaction time and post‐treatment as described in the Experimental part, the total yield of EDTT can rise up to 86.40%, not only a little better than that of EDOT (80.64%, lit 52.…”
Section: Resultsmentioning
confidence: 99%
“…70%). In comparison with other routes,15, 16, 22, 35, 51–54 this transetherification reaction can avoid complex operating procedures and strict reaction conditions. More importantly, by modifying the raw material quantity, reaction time and post‐treatment as described in the Experimental part, the total yield of EDTT can rise up to 86.40%, not only a little better than that of EDOT (80.64%, lit 52.…”
Section: Resultsmentioning
confidence: 99%
“…Usually the side groups such as alkyl chains are incorporated in order to improve solubility of conjugated molecules in organic medium. Other substituents including several functional groups are incorporated to modified physical properties such as energy levels, absorption, emission and morphology [1,2]. Side groups often lead to improved self ordering with enhanced charge mobility [3] in other cases they worsen the electric conductivity due to steric hindrance.…”
Section: Introductionmentioning
confidence: 99%
“…Vibrations at 1186, 1139, and 1080 cm −1 originate from C–O–C bond stretching in the ethylene dioxy group. C–S bond 3 in the thiophene ring are also seen at 977, 833, and 682 cm −1 . The small peaks ranging from 2800 to 3000 cm −1 are assigned to aliphatic C–H stretching mode depending on long alkyl tail of DBSA 4, which confirms the doping of PEDOT by DBSA.…”
Section: Resultsmentioning
confidence: 90%
“…In recent times π‐conjugated organic polymers have generated great interest due to their versatile applications in organic electronics 1. Among them, poly(3,4‐ethylenedioxythiophene) (PEDOT) is one of the most attractive π‐conjugated polymer because of its high electrical conductivity 2, 3, low redox potential 4, moderate band gap 5, transparency in oxidized state 6, environmental stability 7, and easy control of conductivity 8. In the monomer EDOT, thiophene ring is protected at 3 and 4 position by ethylene‐dioxy moiety, reducing the possibility of side chain reaction during polymerization, which leads to enhancement in conjugation length of the resulting polymer chain of PEDOT 9.…”
Section: Introductionmentioning
confidence: 99%