2019
DOI: 10.1080/15421406.2019.1680014
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Synthesis and characterization of fluorene derivatives as organic semiconductors for organic field-effect transistor

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Cited by 9 publications
(2 citation statements)
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“…Different strategies were developed to redshift the absorption of the sulfonium salts, and an efficient strategy was proposed by using fluorene as a π-conjugated spacer [288]. Fluorene is an excellent electron-donating group that was notably used for the design of chromophores for solar cells [289][290][291][292][293][294][295][296][297][298][299], light emitters for OLEDs [300][301][302][303][304][305][306] and charge transport materials for OFETs [307][308][309][310][311][312][313][314][315] and as fluorescent probes [316][317][318][319][320][321][322][323]. The fluorene scaffold was notably used by Yagci and coworkers to design thioxanthone exhibiting a high molar extinction coefficient and a redshifted absorption compared with PI-PAG [324].…”
Section: Fluorene-based Sulfonium Saltsmentioning
confidence: 99%
“…Different strategies were developed to redshift the absorption of the sulfonium salts, and an efficient strategy was proposed by using fluorene as a π-conjugated spacer [288]. Fluorene is an excellent electron-donating group that was notably used for the design of chromophores for solar cells [289][290][291][292][293][294][295][296][297][298][299], light emitters for OLEDs [300][301][302][303][304][305][306] and charge transport materials for OFETs [307][308][309][310][311][312][313][314][315] and as fluorescent probes [316][317][318][319][320][321][322][323]. The fluorene scaffold was notably used by Yagci and coworkers to design thioxanthone exhibiting a high molar extinction coefficient and a redshifted absorption compared with PI-PAG [324].…”
Section: Fluorene-based Sulfonium Saltsmentioning
confidence: 99%
“…[16][17][18] Among many acceptor units, fluorene-based acceptor moieties (e.g., fluorenone) have received attention because of their chemical and thermal stability, low cost, air stability, easy synthesis and purification. [19][20][21][22][23][24][25][26][27][28][29] Although various fluorenone-based organic semiconductors have been reported, their applications have mostly been limited to photovoltaics, with only a few exceptions. 19,20,[25][26][27][28] For instance, fluorenone-based alternating copolymer (PFN-DPPF) containing a furan-based fused aromatic moiety was reported with hole mobility as high as 0.15 cm 2 /Vs.…”
Section: Introductionmentioning
confidence: 99%