Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics

Semiconducting polymers, particularly of the third generation, including donor-acceptor (D-A) copolymers, are extensively studied due to their huge potential for photonic and electronic applications. Here, we report on two new D-A copolymers, CP1 and CP2, composed of different electron-donor (D) uni...

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Main Authors: Věra Cimrová, Petra Babičová, Mariem Guesmi, Drahomír Výprachtický
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/13/22/2939
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author Věra Cimrová
Petra Babičová
Mariem Guesmi
Drahomír Výprachtický
author_facet Věra Cimrová
Petra Babičová
Mariem Guesmi
Drahomír Výprachtický
author_sort Věra Cimrová
collection DOAJ
description Semiconducting polymers, particularly of the third generation, including donor-acceptor (D-A) copolymers, are extensively studied due to their huge potential for photonic and electronic applications. Here, we report on two new D-A copolymers, CP1 and CP2, composed of different electron-donor (D) units: 9-(2-ethylhexyl)carbazole or dibenzothiophene-5,5-dioxide, respectively, and of 4,7-bis(4′-(2-octyldodecyl)thiophen-2′-yl)-5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole building block with central 5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole electron-acceptor (A) units, which were synthesized by Suzuki coupling in the high-boiling solvent xylene and characterized. The copolymers exhibited very good thermal and oxidation stability. A copolymer CP1 with different molecular weights was prepared in order to facilitate a comparison of CP1 with CP2 of comparable molecular weight and to reveal the relationship between molecular weight and properties. The photophysical, electrochemical, and electroluminescence properties were examined. Intense red photoluminescence (PL) with higher PL efficiencies for CP1 than for CP2 was observed in both solutions and films. Red shifts in the PL thin film spectra compared with the PL solution spectra indicated aggregate formation in the solid state. X-ray diffraction measurements revealed differences in the arrangement of molecules in thin films depending on the molecular weight of the copolymers. Light-emitting devices with efficient red emission and low onset voltages were prepared and characterized.
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spelling doaj.art-f8f3ca4fe8534d83a2c7b244df4a6c962023-11-24T14:58:51ZengMDPI AGNanomaterials2079-49912023-11-011322293910.3390/nano13222939Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for PhotonicsVěra Cimrová0Petra Babičová1Mariem Guesmi2Drahomír Výprachtický3Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovského nám. 2, 162 00 Prague 6, Czech RepublicInstitute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovského nám. 2, 162 00 Prague 6, Czech RepublicInstitute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovského nám. 2, 162 00 Prague 6, Czech RepublicInstitute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovského nám. 2, 162 00 Prague 6, Czech RepublicSemiconducting polymers, particularly of the third generation, including donor-acceptor (D-A) copolymers, are extensively studied due to their huge potential for photonic and electronic applications. Here, we report on two new D-A copolymers, CP1 and CP2, composed of different electron-donor (D) units: 9-(2-ethylhexyl)carbazole or dibenzothiophene-5,5-dioxide, respectively, and of 4,7-bis(4′-(2-octyldodecyl)thiophen-2′-yl)-5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole building block with central 5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole electron-acceptor (A) units, which were synthesized by Suzuki coupling in the high-boiling solvent xylene and characterized. The copolymers exhibited very good thermal and oxidation stability. A copolymer CP1 with different molecular weights was prepared in order to facilitate a comparison of CP1 with CP2 of comparable molecular weight and to reveal the relationship between molecular weight and properties. The photophysical, electrochemical, and electroluminescence properties were examined. Intense red photoluminescence (PL) with higher PL efficiencies for CP1 than for CP2 was observed in both solutions and films. Red shifts in the PL thin film spectra compared with the PL solution spectra indicated aggregate formation in the solid state. X-ray diffraction measurements revealed differences in the arrangement of molecules in thin films depending on the molecular weight of the copolymers. Light-emitting devices with efficient red emission and low onset voltages were prepared and characterized.https://www.mdpi.com/2079-4991/13/22/2939donor-acceptor copolymers9-(2-ethylhexyl)carbazoledibenzothiophene-5,5-dioxide5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazolephotophysicselectrochemistry
spellingShingle Věra Cimrová
Petra Babičová
Mariem Guesmi
Drahomír Výprachtický
Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
Nanomaterials
donor-acceptor copolymers
9-(2-ethylhexyl)carbazole
dibenzothiophene-5,5-dioxide
5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole
photophysics
electrochemistry
title Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
title_full Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
title_fullStr Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
title_full_unstemmed Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
title_short Donor-Acceptor Copolymers with 9-(2-Ethylhexyl)carbazole or Dibenzothiophene-5,5-dioxide Donor Units and 5,6-Difluorobenzo[<i>c</i>][1,2,5]thiadiazole Acceptor Units for Photonics
title_sort donor acceptor copolymers with 9 2 ethylhexyl carbazole or dibenzothiophene 5 5 dioxide donor units and 5 6 difluorobenzo i c i 1 2 5 thiadiazole acceptor units for photonics
topic donor-acceptor copolymers
9-(2-ethylhexyl)carbazole
dibenzothiophene-5,5-dioxide
5,6-difluorobenzo[<i>c</i>][1,2,5]thiadiazole
photophysics
electrochemistry
url https://www.mdpi.com/2079-4991/13/22/2939
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AT petrababicova donoracceptorcopolymerswith92ethylhexylcarbazoleordibenzothiophene55dioxidedonorunitsand56difluorobenzoici125thiadiazoleacceptorunitsforphotonics
AT mariemguesmi donoracceptorcopolymerswith92ethylhexylcarbazoleordibenzothiophene55dioxidedonorunitsand56difluorobenzoici125thiadiazoleacceptorunitsforphotonics
AT drahomirvyprachticky donoracceptorcopolymerswith92ethylhexylcarbazoleordibenzothiophene55dioxidedonorunitsand56difluorobenzoici125thiadiazoleacceptorunitsforphotonics