Effect of end group functionalisation of small molecules featuring the fluorene-thiophene-benzothiadiazole motif as emitters in solution-processed red and orange organic light-emitting diodes
Fell, Valentin H.K. and Findlay, Neil J. and Breig, Benjamin and Forbes, Clarissa and Inigo, Anto R. and Cameron, Joseph and Kanibolotsky, Alexander L. and Skabara, Peter J. (2019) Effect of end group functionalisation of small molecules featuring the fluorene-thiophene-benzothiadiazole motif as emitters in solution-processed red and orange organic light-emitting diodes. Journal of Materials Chemistry C, 7 (13). pp. 3934-3944. ISSN 2050-7534 (https://doi.org/10.1039/C8TC02993H)
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Abstract
A series of red fluorescent materials (compounds 1-4), which each contain the symmetric fluorene-thiophene-BT-thiophene-fluorene core, is presented along with their performance in solution-processed OLED devices. Extending the molecular conjugation through end-capping with additional fluorene units (compound 2), or through incorporation of donor functionalities (compounds 3 and 4) improves OLED performance relative to the parent compound 1. Notably, incorporating triphenylamine donor groups in compound 3 led to solution-processed OLED devices operating with a peak luminance of 2888 cd m −2 and a low turn-on voltage (3.6 V).
ORCID iDs
Fell, Valentin H.K., Findlay, Neil J. ORCID: https://orcid.org/0000-0002-1417-3311, Breig, Benjamin ORCID: https://orcid.org/0000-0001-6290-2673, Forbes, Clarissa ORCID: https://orcid.org/0000-0002-2470-0285, Inigo, Anto R., Cameron, Joseph ORCID: https://orcid.org/0000-0001-8622-8353, Kanibolotsky, Alexander L. ORCID: https://orcid.org/0000-0003-3991-6297 and Skabara, Peter J.;-
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Item type: Article ID code: 67875 Dates: DateEvent4 March 2019Published28 February 2019AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Faculty of Engineering > Chemical and Process EngineeringDepositing user: Pure Administrator Date deposited: 16 May 2019 09:19 Last modified: 11 Nov 2024 12:18 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/67875