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Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices

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Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices. / Salunke, Jagadish K.; Wong, F. L.; Feron, Krishna; Manzhos, Sergei; Lo, Ming Fai; Shinde, Durgaprasad; Patil, Abhijeet; Lee, C. S.; Roy, V. A L; Sonar, Prashant; Wadgaonkar, Prakash P.

In: Journal of Materials Chemistry C, Vol. 4, No. 5, 07.02.2016, p. 1009-1018.

Research output: Contribution to journalArticleScientificpeer-review

Harvard

Salunke, JK, Wong, FL, Feron, K, Manzhos, S, Lo, MF, Shinde, D, Patil, A, Lee, CS, Roy, VAL, Sonar, P & Wadgaonkar, PP 2016, 'Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices', Journal of Materials Chemistry C, vol. 4, no. 5, pp. 1009-1018. https://doi.org/10.1039/c5tc03690a

APA

Salunke, J. K., Wong, F. L., Feron, K., Manzhos, S., Lo, M. F., Shinde, D., ... Wadgaonkar, P. P. (2016). Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices. Journal of Materials Chemistry C, 4(5), 1009-1018. https://doi.org/10.1039/c5tc03690a

Vancouver

Salunke JK, Wong FL, Feron K, Manzhos S, Lo MF, Shinde D et al. Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices. Journal of Materials Chemistry C. 2016 Feb 7;4(5):1009-1018. https://doi.org/10.1039/c5tc03690a

Author

Salunke, Jagadish K. ; Wong, F. L. ; Feron, Krishna ; Manzhos, Sergei ; Lo, Ming Fai ; Shinde, Durgaprasad ; Patil, Abhijeet ; Lee, C. S. ; Roy, V. A L ; Sonar, Prashant ; Wadgaonkar, Prakash P. / Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices. In: Journal of Materials Chemistry C. 2016 ; Vol. 4, No. 5. pp. 1009-1018.

Bibtex - Download

@article{ffb93fddc2864c3a823adc328144d05d,
title = "Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices",
abstract = "Due to their easy availability, low cost and opportunities for exploiting reactions of bromo substituents, 1,3,6,8-tetrabromopyrene has attracted major attention in the organic electronics community for designing and constructing novel classes of pyrene based organic semiconducting functional materials. In the present work, 1,3,6,8-tetrabromo pyrene was transformed into the corresponding tetrasubstituted carbazole and phenothiazine derivatives using the classical Suzuki coupling reaction. These newly synthesized materials with a carbazole substituent (PY-CA) and a phenothiazine substituent (PY-PH) were characterised thoroughly and were successfully used as an active light-emitting layer in organic light emitting diodes which resulted in blue and green emission with promising device performance. PY-CA exhibited the maximum brightness at around 2500 cd m-2 and the power efficiency of 1.5 lm W-1 while that of PY-PH exhibited 2116 cd m-2 and 0.45 lm W-1 respectively.",
author = "Salunke, {Jagadish K.} and Wong, {F. L.} and Krishna Feron and Sergei Manzhos and Lo, {Ming Fai} and Durgaprasad Shinde and Abhijeet Patil and Lee, {C. S.} and Roy, {V. A L} and Prashant Sonar and Wadgaonkar, {Prakash P.}",
year = "2016",
month = "2",
day = "7",
doi = "10.1039/c5tc03690a",
language = "English",
volume = "4",
pages = "1009--1018",
journal = "Journal of Materials Chemistry C",
issn = "2050-7526",
publisher = "Royal Society of Chemistry",
number = "5",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Phenothiazine and carbazole substituted pyrene based electroluminescent organic semiconductors for OLED devices

AU - Salunke, Jagadish K.

AU - Wong, F. L.

AU - Feron, Krishna

AU - Manzhos, Sergei

AU - Lo, Ming Fai

AU - Shinde, Durgaprasad

AU - Patil, Abhijeet

AU - Lee, C. S.

AU - Roy, V. A L

AU - Sonar, Prashant

AU - Wadgaonkar, Prakash P.

PY - 2016/2/7

Y1 - 2016/2/7

N2 - Due to their easy availability, low cost and opportunities for exploiting reactions of bromo substituents, 1,3,6,8-tetrabromopyrene has attracted major attention in the organic electronics community for designing and constructing novel classes of pyrene based organic semiconducting functional materials. In the present work, 1,3,6,8-tetrabromo pyrene was transformed into the corresponding tetrasubstituted carbazole and phenothiazine derivatives using the classical Suzuki coupling reaction. These newly synthesized materials with a carbazole substituent (PY-CA) and a phenothiazine substituent (PY-PH) were characterised thoroughly and were successfully used as an active light-emitting layer in organic light emitting diodes which resulted in blue and green emission with promising device performance. PY-CA exhibited the maximum brightness at around 2500 cd m-2 and the power efficiency of 1.5 lm W-1 while that of PY-PH exhibited 2116 cd m-2 and 0.45 lm W-1 respectively.

AB - Due to their easy availability, low cost and opportunities for exploiting reactions of bromo substituents, 1,3,6,8-tetrabromopyrene has attracted major attention in the organic electronics community for designing and constructing novel classes of pyrene based organic semiconducting functional materials. In the present work, 1,3,6,8-tetrabromo pyrene was transformed into the corresponding tetrasubstituted carbazole and phenothiazine derivatives using the classical Suzuki coupling reaction. These newly synthesized materials with a carbazole substituent (PY-CA) and a phenothiazine substituent (PY-PH) were characterised thoroughly and were successfully used as an active light-emitting layer in organic light emitting diodes which resulted in blue and green emission with promising device performance. PY-CA exhibited the maximum brightness at around 2500 cd m-2 and the power efficiency of 1.5 lm W-1 while that of PY-PH exhibited 2116 cd m-2 and 0.45 lm W-1 respectively.

U2 - 10.1039/c5tc03690a

DO - 10.1039/c5tc03690a

M3 - Article

VL - 4

SP - 1009

EP - 1018

JO - Journal of Materials Chemistry C

JF - Journal of Materials Chemistry C

SN - 2050-7526

IS - 5

ER -