Issue 46, 2015

Platinum(ii) polymetallayne-based phosphorescent polymers with enhanced triplet energy-transfer: synthesis, photophysical, electrochemistry, and electrophosphorescent investigation

Abstract

Two series of new phosphorescent copolymers with bicarbazole-based platinum(II) polymetallayne backbones have been successfully prepared through Sonogashira cross-coupling with different IrIII ppy-type (ppy = 2-phenylpyridine anion) complexes as phosphorescent centers. The photophysical investigations not only indicate a highly efficient triplet energy-transfer process from the polymetallayne segments to the phosphorescent units in the polymer solution, but also figure out the structure–property relationship between the triplet energy-transfer process and the energy-levels of different excited states. In addition, the phosphorescent copolymers can produce yellow-emitting phosphorescent OLEDs (PHOLEDs) with high EL efficiencies and a current efficiency (ηL) of 11.49 cd A−1, an external quantum efficiency (ηext) of 4.38%, a power efficiency (ηP) of 3.78 lm W−1, and red-emitting PHOLEDs with a ηL of 5.86 cd A−1, ηext of 10.1%, and a ηP of 2.29 lm W−1, representing very decent electroluminescent performances achieved by the phosphorescent copolymers. Herein, this work not only furnishes very important clues for further polishing of this category novel phosphorescent polymer, but also provides a new approach to the design and synthesis of highly efficient phosphorescent copolymers.

Graphical abstract: Platinum(ii) polymetallayne-based phosphorescent polymers with enhanced triplet energy-transfer: synthesis, photophysical, electrochemistry, and electrophosphorescent investigation

Supplementary files

Article information

Article type
Paper
Submitted
02 Mar 2015
Accepted
31 Mar 2015
First published
01 Apr 2015

RSC Adv., 2015,5, 36507-36519

Platinum(II) polymetallayne-based phosphorescent polymers with enhanced triplet energy-transfer: synthesis, photophysical, electrochemistry, and electrophosphorescent investigation

Z. Huang, B. Liu, J. Zhao, Y. He, X. Yan, X. Xu, G. Zhou, X. Yang and Z. Wu, RSC Adv., 2015, 5, 36507 DOI: 10.1039/C5RA03697F

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