Spiro [fluorene-9, 9-xanthene]-class hole transport material and application thereof
A hole-transporting material, xanthene technology, applied in photovoltaic power generation, electrical components, circuits, etc., can solve problems such as commercial application limitations, achieve efficient separation and transport of charges, facilitate large-scale commercial preparation, high hole Effects of Mobility and Conductivity
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[0059] The preparation method of the spiro[fluorene-9,9-oxanthene] type hole transport material of the present invention adopts different synthesis schemes according to the number of different N-nuclear structural units to be prepared. According to the number of N-nuclear structural units and the number of spiro[fluorene-9,9-oxanthene] in the target product, those skilled in the art can designate an appropriate synthesis scheme according to the prior art. The applicant first provides a synthesis method of a class of more specific products, aiming to guide those skilled in the art to use similar methods to complete the synthesis of other compounds. Described synthetic method comprises the steps:
[0060] (1) Under nitrogen protection, at room temperature, add dry toluene, 3 molar parts of 2,7-dibromospiro[fluorene-9,9-oxanthene], 0.02 molar parts of palladium acetate, 0.04 Molar parts of 1,1′-bis(diphenylphosphino)ferrocene, 1 molar part of 4,4′-dimethoxydiphenylamine and 1.5 ...
Embodiment 1
[0067] N2-(2-(bis(4-methoxyphenyl)amine)spiro[fluorene-9,9′-oxanthene]-7-yl)-N2,N7,N7-tetrakis(4-methoxyphenyl) ) spiro[fluorene-9,9'-oxanthene]-2,7-diamine (X26) synthesis, according to the following route:
[0068]
[0069] (1) Synthesis of 7-bromo-N,N-bis(4-methoxybenzene)spiro[fluorene-9,9′-oxanthene]-2-amine (TBrSFX):
[0070]Under nitrogen protection, at room temperature, dry toluene (20ml), 2,7-dibromospiro[fluorene-9,9-oxanthene] (2.94g, 6.0mmol), palladium acetate (9.0mg , 0.04mmol), 1,1'-bis(diphenylphosphino)ferrocene (44.4mg, 0.08mmol), 4,4'-dimethoxydiphenylamine (0.46g, 2.0mmol) and tert-butanol Sodium (0.29g, 3.0mmol) was stirred overnight at 100°C. After cooling, the reaction was quenched with water, extracted with ethyl acetate, dried over anhydrous sodium sulfate, and separated by silica gel column chromatography to obtain 1.00 g of a light yellow solid with a yield of 78%. It was identified as 7-bromo-N,N-bis(4-methoxybenzene)spiro[fluorene-9,9′-oxanth...
Embodiment 2
[0076] N2,N2″-([1,1′-biphenyl]-4,4′-diyl)bis(N2,N7,N7-tetrakis(4-methoxybenzene)spiro[fluorene-9,9′- The synthesis of xanthene]-2,7-diamine (X36) follows the following route:
[0077]
[0078] Specifically, the final product was prepared by using a one-pot Fabuchwald (Buchwald) reaction: under nitrogen protection, at room temperature, dry toluene (10 mL), tris(dibenzylideneacetone) dipalladium (3.1 mg , 0.03mmol), 1,1′-bis(diphenylphosphino)ferrocene (DPPF) (5.2mg, 0.05mmol) and 4,4′-dibromo-1,1′-biphenyl (156mg, 0.5 mmol), stirred for 10 minutes. Next, sodium tert-butoxide (120mg, 1.25mmol) and p-methoxyaniline (123mg, 1.00mmol) were added to the solution, and the temperature was raised to 90°C for 8 hours of reaction. Thereafter, trace the plate with TLC until the raw material spots disappear. Then, sodium tert-butoxide (120 mg, 1.25 mmol), TBrSFX (670.5 mg, 1.05 mmol) and toluene were added. The solution was warmed to 100°C and stirred overnight. After the reaction,...
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