4.6 Article

Rational utilization of intramolecular and intermolecular hydrogen bonds to achieve desirable electron transporting materials with high mobility and high triplet energy

Journal

JOURNAL OF MATERIALS CHEMISTRY C
Volume 4, Issue 7, Pages 1482-1489

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5tc04198h

Keywords

-

Funding

  1. National Basic Research Programs of China (973 Programs) [2013CB834805, 2015CB655002]
  2. National Natural Science Foundation of China [91433201, 51125013, 61575146]
  3. Innovative Research Group of Hubei Province [2015CFA014]
  4. Fundamental Research Funds for the Central Universities of China [2042015KF0190]

Ask authors/readers for more resources

Three new pyrimidine-containing star-shaped compounds, namely, 1,3,5-tri(3-(pyrimidin-5-yl)phenyl)-benzene (TPM-TPB), 2,4,6-tris(3-(pyrimidin-5-yl)phenyl)-1,3,5-triazine (TPM-TAZ) and 3,5,6-tris(3-(pyrimidin-5-yl)phenyl)-1,2,4-triazine (TPM-i-TAZ), were synthesized and characterized. These new compounds exhibited favorable electronic affinity (E-a >2.81 eV) and the triplet energy levels (E-T) up to similar to 2.83 eV. X-ray diffraction analysis of the compounds revealed that the intramolecular and intermolecular C-H center dot center dot center dot N hydrogen bonds of TPM-TAZ resulted in high electron mobility up to 2.0 x 10(-3) cm(2) V-1 s(-1). Using these compounds as the electron transporting materials, the blue phosphorescent organic light-emitting devices showed good performance, with a very low turn-on voltage of 2.4 V, a maximum current efficiency of 26.4 cd A(-1), and a maximum power efficiency of 26.9 lm W-1.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available