2012
DOI: 10.1002/macp.201100591
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Synthesis and Photovoltaic Properties of 1,8‐Carbazole‐Based Donor–Acceptor Type Conjugated Polymers

Abstract: 1,8-Diethynylcarbazole-based conjugated polymers were synthesized by the acetylenic oxidative coupling reaction or Pd-catalyzed Sonogashira reaction of the newly designed 3,6-dialkylated 1,8-diethynylcarbazole monomers. In particular, the Sonogashira polycondensation was effective for the preparation of donor-acceptor type alternating copolymers. The UV-vis absorption and fl uorescence spectra of the polymers revealed the strength of the donor-acceptor interactions as well as their self-assembling features. Th… Show more

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Cited by 12 publications
(20 citation statements)
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“…Fujita and Michinobu [ 178 ] synthesized a carbazole-based conjugated polymer as donor–acceptor type alternating copolymers. Different type of poly(1,8-diethynylcarbazole) were synthesized and their fluorescence and electrochemical properties were evaluated being adequate to be used as a p-type semiconductor in solar cells.…”
Section: Applicationmentioning
confidence: 99%
“…Fujita and Michinobu [ 178 ] synthesized a carbazole-based conjugated polymer as donor–acceptor type alternating copolymers. Different type of poly(1,8-diethynylcarbazole) were synthesized and their fluorescence and electrochemical properties were evaluated being adequate to be used as a p-type semiconductor in solar cells.…”
Section: Applicationmentioning
confidence: 99%
“…A sharp absorption band at 1047 cm −1 corresponds to the presence of a sugar unit [34]. Some scattered small peaks were observed at 633,618 and 579 cm −1 which reveals the presence of alkane derivatives in the EPS[35].…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of BT , BT2 , DTBT , DTBT2 , PSN , and PSeN are reported elsewhere. DPP , isoindigo , NDI , and BBT were newly synthesized by the following general procedure (Scheme ): A solution of 3,6-di- tert -butyl-1,8-diethynyl-9-hexadecyl-9 H -carbazole (0.1134 g 0.2000 mmol) and dibromo-comonomer (0.2000 mmol), namely, 3,6-bis­(5-bromothiophen-2-yl)-2,5-dioctyl-2,5-dihydropyrrolo­[3,4- c ]­pyrrole-1,4-dione, ( E )-6,6′-dibromo-1,1′-dioctyl-[3,3′-biindolinylidene]-2,2′-dione, 4,9-dibromo-2,7-dioctylbenzo­[ lmn ]­[3,8]­phenanthroline-1,3,6,8­(2 H ,7 H )-tetraone, and 4,7-bis­[5-bromo-4-(2-butyloctyl)­thiophen-2-yl]­benzo­[1,2- c :4,5- c ’]­bis­[1,2,5]­thiadiazole, respectively, in 3 mL of toluene and 1 mL of i Pr 2 NH was degassed with nitrogen for 15 min. PdCl 2 (PPh 3 ) 2 (5.7 mg, 0.008 mmol) and CuI (1.5 mg, 0.008 mmol) were added.…”
Section: Methodsmentioning
confidence: 99%