Polymer or micro-molecular material having molecular main chain comprising benzophene group, preparation method and application thereof
A technology of benzodisulfone phenyl and benzodisulfone phene, which is applied in the field of organic solar cells, can solve the problems of low carrier mobility, narrow absorption spectrum, poor stability, etc., achieve broad absorption spectrum and enhance molar absorption coefficient, the effect of improving coplanarity
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Embodiment 1
[0028] In the present embodiment, the polymer structural formula is as follows:
[0029]
[0030] The preparation of this polymer comprises the steps:
[0031] (1) Synthesis of benzodisulfone phenyl acceptor unit
[0032]
[0033] 0.3 g of compound 1, 0.3 g of m-chloroperoxybenzoic acid (mCPBA) and 20 mL of dichloromethane were added to a round-necked flask, and the reaction was stirred at room temperature for 24 hours. After the reaction was completed, spin-dried and passed through a silica gel column to obtain a yellow product 3 with a mass of 0.19 g and a yield of 57%.
[0034] 1 H-NMR (400MHz, CDCl 3 ):δ7.44(d,2H),6.73(d,2H),4.45(t,4H),2.0-1.81(m,4H),1.55-1.45(m,4H),1.39-1.33(m,8H ), 0.89(t,6H). The calculated molecular weight is C 26 h 36 Br 2 o 6 S 2 ,666.03, the actual mass spectrum is as figure 2 shown.
[0035] (2) Preparation of polymer donor material
[0036]
[0037] In the three-necked flask, add 0.1g compound 4, 0.074g compound 3 and 10mL t...
Embodiment 2
[0041] In the present embodiment, the polymer structural formula is as follows:
[0042]
[0043] The preparation of this polymer comprises the steps:
[0044]
[0045] Add 0.1 g of compound 3, 0.061 g of 2,5-trimethyltinthiophene and 10 mL of toluene into a three-necked flask, replace nitrogen three times, add (4 mg of catalyst tris(dibenzylideneacetone) dipalladium and 4.63 mg of triphenylphosphine , Replace nitrogen three times again, and react under reflux for 24 hours. After the reaction, the product is carried out for Soxhlet extraction, using methanol, acetone and n-hexane as solvents, and finally using toluene to obtain 52 mg of the polymer product, with a yield of 59%. 1 H-NMR (400MHz, CDCl 3 ):δ7.4-7.3(m,2H),7.1-6.9(m,2H),4.1-3.8(m,4H),2.0-1.9(m,2H),1.3-1.2(m,16H),1 -0.9(m,12H).
[0046] The above-prepared polymers can be used as donor materials in organic solar cells. The structure of the organic solar cell is as figure 1 As shown, the anode is made of in...
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