A kind of polymer based on phenazine trimer and its preparation method and battery application
A technology of phenazine trimer and polymer, which is applied in battery electrodes, circuits, electrical components, etc., can solve the problems of low actual capacity and dependence on scarce natural resources, and achieve reduced production costs, abundant material sources, and improved stability Effect
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Embodiment 1
[0045] Example 1: Synthesis of p-TPZB1
[0046] 1.TPZB (X=Z=H, Y=CH=CH 2 )Synthesis
[0047]
[0048] 5,10-dihydrophenazine (5.47g, 30mmol), 1,3,5-tribromobenzene (3.15g, 10mmol), 4-bromostyrene (5.49g, 30mmol), palladium acetate (202mg, 1.8mmol ), xPhos (1.72g, 3.6mmol), sodium tert-butoxide (8.65g, 90mmol) and toluene (30ml) were put into the reaction flask, and oxygen was removed by freezing-vacuum-thawing cycle 3 times. The mixture was condensed under reflux at 100° C. and stirred for 12 hours. After the obtained crude product was cooled to room temperature, it was purified by column chromatography with neutral alumina (DCM:PE=1:2 to 1:1), and then recrystallized (mixture of DCM and MeOH). 1 H NMR (400MHz, C6D6, ppm) δ = 7.28 (d, J = 8.4Hz, 6H), 7.18 (d, J = 3.3Hz, 9H), 6.56 (dd, J = 17.6, 10.9Hz, 3H), 6.38 (dtd, J=23.1,7.5,1.4Hz,12H),6.15(dd,J=7.7,1.4Hz,6H),5.93(dd,J=7.8,1.4Hz,6H),5.61(d,J=17.5 Hz,3H),5.14(d,J=11.1Hz,3H).13C NMR(101MHz,C6D6,ppm)δ=146.37,139.71,137...
Embodiment 2
[0051] Embodiment 2: the synthesis of TPZB-6COOLi
[0052]
[0053] 1. Synthesis of TPZB-6COOMe
[0054] 5,10-dihydrophenazine (2.73g, 15mmol), 1,3,5-tribromobenzene (1.57g, 5mmol), dimethyl 5-bromo-isophthalate (4.1g, 15mmol), acetic acid Palladium (100mg, 0.9mmol), xPhos (860mg, 1.8mmol), cesium carbonate (14.7g, 90mmol) and . Toluene (30ml) was put into the reaction bottle, and the oxygen was removed by freezing-vacuum-thawing cycle 3 times. The mixture was refluxed and condensed at 130°C for 12 hours with stirring. The obtained crude product was quenched with methanol, cooled to room temperature, purified by column chromatography with neutral alumina (PE:EA=3:1), and recrystallized (mixture of DCM and MeOH). 1 H NMR (400MHz, C6D6, ppm) δ = 9.05 (t, J = 1.6Hz, 1H), 8.42 (d, J = 1.6Hz, 2H), 7.32 (s, 1H), 6.43 (td, J = 7.8, 1.3Hz, 3H), 6.31(td, J=7.8, 1.3Hz, 3H), 6.21(dd, J=7.9, 1.2Hz, 3H), 5.81(dd, J=7.9, 1.2Hz, 3H), 3.41( s,6H).
[0055] 2. Synthesis of TPZB-6COOLi...
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