Novel light-emitting compound and organic light-emitting element containing same
A technology of light-emitting compounds and chemical formulas, applied in the field of new light-emitting compounds and organic light-emitting elements, can solve the problems of high driving voltage, practical difficulties, short life, etc., and achieve the effects of low driving voltage, low power consumption, and long life.
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Embodiment 1
[0148] Embodiment 1: the synthesis of compound 1
[0149]
[0150] 4.0g of the above intermediate A3, 4.1g of 1-bromo-3-iodobenzene, 1.7g of t-BuONa, 0.45g of Pd 2 (dba) 3 , 0.6ml of (t-Bu) 3 P was dissolved in 60ml of toluene, and then stirred under reflux. After the termination of the reaction was confirmed by TLC, the organic layer was extracted with MC, filtered under reduced pressure, and purified on a column to obtain 2.05 g of intermediate 1-1 (yield 35%).
[0151] 2.05g of the above intermediate 1-1, 2.05g of intermediate B1, 0.61g of t-BuONa, 0.15g of Pd 2 (dba) 3 , 0.2ml of (t-Bu) 3 P was dissolved in 30 ml of toluene, and then stirred under reflux. After the termination of the reaction was confirmed by TLC, the organic layer was extracted with MC, filtered under reduced pressure, and purified on a column to obtain 1.34 g of compound 1 (yield 52%).
[0152] m / z: 613.22 (100.0%), 614.22 (47.9%), 615.22 (11.8%), 616.23 (1.7%), 614.21 (1.1%)
Embodiment 2
[0153] Embodiment 2: the synthesis of compound 2
[0154]
[0155] Compound 2 was synthesized by the same method as Compound 1 except that Intermediate A1 was used instead of Intermediate A3.
[0156] m / z: 538.17 (100.0%), 539.17 (42.2%), 540.17 (8.9%), 541.18 (1.3%)
Embodiment 3
[0157] Embodiment 3: the synthesis of compound 3
[0158]
[0159] Compound 3 was synthesized by the same method as Compound 1, except that Intermediate A2 was used instead of Intermediate A3, and Intermediate B2 was used instead of Intermediate B1.
[0160] m / z: 570.12 (100.0%), 571.13 (41.4%), 572.12 (9.4%), 572.13 (9.0%), 573.12 (3.9%), 571.12 (2.3%), 573.13 (1.3%)
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