4.4 Article

Aromatic substituents for prohibiting side-chain packing and π-π stacking in tin-cored tetrahedral stilbenoids

Journal

ELECTRONIC MATERIALS LETTERS
Volume 12, Issue 3, Pages 388-398

Publisher

KOREAN INST METALS MATERIALS
DOI: 10.1007/s13391-016-6002-8

Keywords

organic light emitting diode; tin-cored; aromatic substituents; pi-pi stacking

Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MSIP) [2014R1A2A1A11051098]
  2. International Cooperative R&D program through the Korea Institute for Advancement of Technology (KIAT) - Ministry of Trade, Industry, and Energy (MOTIE) of Korea
  3. National Research Foundation of Korea [2014R1A2A1A11051098] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Tetrahedral structures comprising Sn-cored materials with five different types of substituents were synthesized. For the substituents, we employed methyl and tert-butyl as aliphatic groups, and naphthyl and phenyl as aromatic groups. The bandgap is in the range of 3.28 - 3.56 eV. The All the compounds with substituents showed bathochromical photoluminescence characteristics and exhibited aggregation-induced emission characteristics. Specifically, the compounds with aromatic substituents prohibited side-chain packing and pi-pi stacking. The energy levels of the highest occupied and lowest unoccupied molecular orbitals were measured to be 5.5 - 5.75 and 2.0 - 2.37 eV, respectively. The maximum luminance efficiencies and power efficiencies of the Sn-cored compound-based organic light-emitting diodes (OLEDs) were 0.38 - 0.71 cd/A and 0.15 - 0.28 lm/W. Therefore, it is expected that Sn-cored compounds with a tetrahedral structure, especially those containing aromatic substituents, can be used as an active material in blue OLEDs for prohibiting side-chain packing and pi-pi stacking.

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