Compound for organic electrical element, organic electrical element using compound, and electronic device therefor
a technology of organic electric elements and compounds, applied in the direction of luminescent compositions, organic chemistry, chemistry apparatus and processes, etc., can solve the problems of increasing the size of the portable display market, increasing the cost of power consumption, and reducing the efficiency of the device, so as to achieve high heat resistance, low driving voltage, and high luminous efficiency
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of 2-21
[0099]
[0100]A Sub 2 (6.4 g, 20 mmol) was added to a round bottom flask, and a Sub 3 (7.4 g, 20 mmol) was added, and 7.4 g of the product was obtained by the synthesis method of 1-1 above. (Yield: 76%).
TABLE 1compoundFD-MScompoundFD-MS1-1m / z = 473.12(C34H19NS = 473.59)1-2m / z = 473.12(C34H19NS = 473.59)1-3m / z = 473.12(C34H19NS = 473.59)1-4m / z = 599.17(C44H25NS = 599.74)1-5m / z = 457.15(C34H19NO = 457.52)1-6m / z = 457.15(C34H19NO = 457.52)1-7m / z = 457.15(C34H19NO = 457.52)1-8m / z = 748.25(C56H32N2O = 748.87)1-9m / z = 483.20(C37H25N = 483.60)1-10m / z = 683.26(C53H33N = 683.84)1-11m / z = 605.21(C47H27N = 605.72)1-12m / z = 610.24(C46H30N2 = 610.74)1-13m / z = 473.12(C34H19NS = 473.59)1-14m / z = 473.12(C34H19NS = 473.59)1-15m / z = 473.12(C34H19NS = 473.59)1-16m / z = 523.14(C38H21NS = 523.65)1-17m / z = 457.15(C34H19NO = 457.52)1-18m / z = 457.15(C34H19NO = 457.52)1-19m / z = 457.15(C34H19NO = 457.52)1-20m / z = 507.16(C38H21NO = 507.58)1-21m / z = 483.20(C37H25N = 483.60)1-22m / z = 657.25(C51H31N = 657.80...
example 1
Manufacture and evaluation of Green Organic Light Emitting Device (Phosphorescent Host)
[0102]An organic electroluminescent device was fabricated according to a conventional method using a compound obtained through synthesis as a host material of an emitting layer. First, on an ITO layer(anode) formed on a glass substrate, N1-(naphthalen-2-yl)-N4,N4-bis(4-(naphthalen-2-yl(phenyl)amino)phenyl)-N1-phenyl benzene-1,4-diamine(hereinafter will be abbreviated as 2-TNATA) was vacuum-deposited to form a hole injection layer with a thickness of 60 nm, and subsequently, on this film, 4,4-bis [N-(1-naphthyl)-N-phenylaminolbiphenyl (hereinafter will be abbreviated as NPB) as a hole transporting compound was vacuum-deposited to form a hole transport layer with a thickness of 60 nm. On the hole transport layer, the inventive compound or comparative compound A [CBP(4,4′-N,N-dicarbazole-biphenyl)] or comparative compound B or comparative compound C were used as a host, and as a dopant, an emitting l...
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