A kind of semiconductor conjugated polymer and preparation method thereof
A conjugated polymer and semiconductor technology, applied in the field of semiconductor conjugated polymers and their preparation, can solve the problems of high use cost, influence on device current, weak PCBM absorption, etc.
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[0029] The preparation method of each monomer is described as follows:
[0030] Preparation of two-dimensional conjugated benzodithiophene bistin monomer
[0031] The schematic diagram of the synthetic route of the two-dimensional conjugated benzodithiophene ditin monomer is shown in figure 2 As shown, the bistin monomer was prepared by the literature method, and the detailed preparation method can be found in the literature report (PolymerChemistry, 2013, 4, 536-541.).
[0032] Preparation of (2-oxindol-3-ylidene)benzodifuran-dione dibromomonomers
[0033] The synthetic route of (2-oxindol-3-ylidene)benzodifuran-dione dibromomonomer is as follows figure 2 shown. For the detailed preparation method, please refer to the literature report (Chemical Communication, 2013, 49, 3790-3792.).
Embodiment 1
[0034] Embodiment 1, synthetic polymer P1
[0035] The synthetic route of polymer P1 is as follows image 3 As shown, the specific steps are: add 0.5mmol of bis-tin monomer and 0.5mmol of bis-bromine monomer (R1 and R2 are shown in Table 1) into a 100mL reaction bottle, then add 10mL of anhydrous toluene, replace with nitrogen for 40 minutes, Add 2% catalyst tris(dibenzylideneacetone) dipalladium, use tris(o-methylphenyl)phosphorus as ligand, react at 110oC for 24 hours, cool the reaction to room temperature, add 200mL of methanol to precipitate, filter the solid, respectively Soxhlet extraction with methanol and n-hexane for 24 hours, and then Soxhlet extraction with chloroform for 24 hours, and finally the liquid was rotary evaporated, methanol precipitated to obtain a black polymer.
Embodiment 2-3
[0037] The specific steps are the same as in Example 1: add 0.5 mmol of bistin monomer and 0.5 mmol of bis-bromine monomer (R1 and R2 are shown in Table 1) into a 100 mL reaction bottle, add 10 mL of anhydrous toluene, replace with nitrogen for 40 minutes, and add 2% Catalyst tris(dibenzylideneacetone)dipalladium, with tris(o-methylphenyl)phosphorus as ligand, react at 110oC for 24 hours, cool to room temperature, add 200mL of methanol to precipitate, and the solid is Soxhlet with methanol and n-hexane respectively Extracted for 24 hours, then Soxhlet extracted with chloroform for 24 hours, and finally the liquid was rotary evaporated, and methanol precipitated to obtain black polymers P2-P3, the specific structure of which is shown in Table 1.
[0038] Figure 4 The absorption spectrum of polymer P1 is given, and the absorption peak covers visible light and extends to the near-infrared region. Figure 5 The electrochemical curve of polymer P1 is given, and it can be concluded ...
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