2019
DOI: 10.1021/acs.chemmater.9b03525
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Indacenodithiazole-Ladder-Type Bridged Di(thiophene)-Difluoro-Benzothiadiazole-Conjugated Copolymers as Ambipolar Organic Field-Effect Transistors

Abstract: A series of four donor–acceptor conjugated copolymers P1–P4 with linear and branched side chains based on a ladder-type indacenodithiazole (IDTz) moiety containing an electron-deficient thiazole unit are copolymerized with di-2-thienyl-2,1,3-benzothiadiazole (DTBT) and 4,7-di­(thien-2-yl)-5,6-difluoro-2,1,3-benzothiadiazole (DTBTff) as building blocks. Their optical, electrochemical, and thermal properties and charge transport behavior in organic field-effect transistors (OFETs) are studied. All copolymers exh… Show more

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Cited by 29 publications
(18 citation statements)
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“…A variety of IDT copolymers (Fig. 4, Pp9–12) showed appreciable hole and electron mobilities, 0.87 and 0.50 cm 2 V −1 s −1 , respectively, and high thermal stability with only 5% weight loss at 365 °C 53 . However, these measurements were not performed in tandem.…”
Section: Improving Ofet Lifetime Through Osc Designmentioning
confidence: 99%
“…A variety of IDT copolymers (Fig. 4, Pp9–12) showed appreciable hole and electron mobilities, 0.87 and 0.50 cm 2 V −1 s −1 , respectively, and high thermal stability with only 5% weight loss at 365 °C 53 . However, these measurements were not performed in tandem.…”
Section: Improving Ofet Lifetime Through Osc Designmentioning
confidence: 99%
“…Although the reaction is very stable to oxygen and moisture and tolerates numerous functional groups, it raises the environmental issue seriously for the employment of the toxic organostannanes [89]. Under microwave irradiation, nevertheless, the reaction has been widely employed in polymerizations [90] and few protocols have been developed and published during the last two decades. Microwave-accelerated one-pot hydrostannylation/Stille coupling reaction was reported for the conversion of 1-alkynes to 1,3-dienes or styrenes.…”
Section: Stille Cross-coupling Reactionmentioning
confidence: 99%
“…Microwave‐assisted chemistry started to empower researchers toward important innovations in advanced nanomaterial design and development. It quantitatively and selectively allows facile emergence of valuable organic compounds, polymers and nanomaterials in extremely short reaction time than by applying conventional heating [22–24] . Additionally, the use of microwave irradiation heating offers significant energy‐saving processes with low level of formation of side reactions; therefore, it accomplishes the conditions of green chemistry.…”
Section: Introductionmentioning
confidence: 99%
“…It quantitatively and selectively allows facile emergence of valuable organic compounds, polymers and nanomaterials in extremely short reaction time than by applying conventional heating. [22][23][24] Additionally, the use of microwave irradiation heating offers significant energy-saving processes with low level of formation of side reactions; therefore, it accomplishes the conditions of green chemistry. Microwave heating could be designateed as a Bunsen burner of the current century, as it is predominantly used.…”
Section: Introductionmentioning
confidence: 99%