Electron transport material and organic electroluminescent device
An electron transport material, an unreplaced technology, applied in the field of organic electroluminescent devices, can solve the problems of high cost, instability, and many steps, and achieve the effects of high stability, high charge transfer ability, and high glass transition temperature
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Embodiment 1
[0042] The synthetic method for preparing compound A is the same as the synthetic method for preparing the compound of formula I. The structures of compounds 2, 3, 4, 5 and 6 are
[0043]
[0044] The yield of compound A was 82%. Characterization data: melting point (DSC) 289°C, purity 99.9%; 1 H NMR (400MHz, CDCl 3 )δ (ppm): 8.06 (m, 1H), 7.80 (s, 1H), 7.61 (m, 1H), 7.56 (m, 1H), 7.48 (m, 2H), 7.44 (m, 1H), 7.32 ( m,2H),7.30(m,5H),7.24(m,1H),7.22(m,1H),7.14(m,4H),7.08(m,2H),7.06(m,4H).
Embodiment 2
[0046] The synthetic method for preparing compound B is the same as the synthetic method for the compound of formula I. The structures of compounds 2, 3, 4, 5 and 6 are
[0047]
[0048]
[0049] The yield of compound B was 76%. Characterization data: melting point (DSC) 342°C, purity 99.9%; 1 H NMR (400MHz, CDCl 3 )δ (ppm): 8.06 (m, 1H), 7.80 (s, 1H), 7.61 (m, 1H), 7.56 (m, 1H), 7.48 (m, 6H), 7.44 (m, 1H), 7.32 ( m,6H),7.24(m,1H),7.22(m,3H),7.14(m,4H),7.08(m,2H),7.06(m,4H).
Embodiment 3
[0051] The synthetic method for preparing compound C is the same as the synthetic method for synthesizing the compound of formula I. The structures of compounds 2, 3, 4, 5 and 6 are
[0052]
[0053]
[0054] The yield of compound C was 79%. Characterization data: melting point (DSC) 302°C, purity 99.9%; 1 H NMR (400MHz, CDCl 3 )δ (ppm): 8.41 (m, 2H), 8.06 (m, 1H), 7.80 (s, 1H), 7.61 (s, 1H), 7.56 (m, 1H), 7.48 (m, 4H), 7.44 ( m,1H),7.32(m,4H),7.30(m,5H),7.24(m,1H),7.22(m,2H),7.14(m,2H),7.08(m,1H),7.06(m ,2H).
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