Dendritic hyperbranched polymer as well as preparation method and use thereof
A hyperbranched polymer and dendritic technology, applied in instruments, optics, nonlinear optics, etc., can solve the problems of transmission speed, capacity and space compatibility limit, it is difficult to meet the requirements of future communication technology, and achieve high-level First-order nonlinear optical effect and stability, good three-dimensional separation effect, high yield effect
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Embodiment 1
[0032] Synthesis of dendritic hyperbranched polymer DHPG0:
[0033] 1) In a 50mL Schlenk tube, add compound G0 (124.1mg, 2mmol), N-(6-azido)-3,6-dibromocarbazole (99mg, 2.2mmol), CuSO 4 ·5H 2 O (10mol%), 20% NaHCO 3 (20mol%) and sodium ascorbate (20mol%). Under argon protection, 5 mL of THF and 1 mL of water were added after deoxygenation, and reacted at room temperature for 3 hours. Water was added to the reaction system to quench the reaction. Extract with chloroform, combine the organic phases and spin dry with a rotary evaporator. The crude product was separated by silica gel column chromatography using chloroform / ethyl acetate (2 / 1, V / V) as the eluent to obtain 102 mg of a red solid with a yield of 95%.
[0034] IR(KBr),υ(cm -1 ):1723(C=O),1511,1341(-NO 2 ).
[0035] 1 H NMR (CDCl 3 ,300MHz)δ(TMS,ppm):1.26(s,br,4H,-CH 2 -),1.78(m,4H,-CH 2 -),2.32(t,J=6.9Hz,2H,-CH 2 C-),2.99(t,J=7.2Hz,2H,-CH 2 -),3.94(t,J=5.4Hz,2H,-NCH 2 -),4.21(t,J=6Hz,4H,-NCH 2 -),4.26(t,...
Embodiment 2
[0044] Synthesis of dendritic hyperbranched polymer DHPG1:
[0045] 1) In a 50mL Schlenk tube, add compound G1 (170.9mg, 1mmol), N-(6-azidohexyl)-3,6-dibromocarbazole (90mg, 2mmol), and add 5mL THF after deoxygenation, 0.25mL of 0.04mmol / mL CuSO 4 (10mol%) aqueous solution, 0.25mL of 0.08mmol / mL sodium pitascorbate (20mol%) aqueous solution, reacted at room temperature for 3 hours. An appropriate amount of water was added to the reaction system to quench the reaction. Extract with chloroform, combine the organic phases and spin dry with a rotary evaporator. The crude product was separated by silica gel column chromatography using chloroform / ethyl acetate (2 / 1, V / V) as the eluent to obtain 200 mg of a red solid with a yield of 93%.
[0046] IR(KBr),υ(cm -1 ):1723(C=O),1511,1341(-NO 2 ).
[0047] 1 H NMR (CDCl 3 ,300MHz)δ(TMS,ppm):0.94(t,J=7.2Hz,4H,-CH 2 -),1.26(s,br,4H,-CH 2 -),1.77(s,br,2H,-CH 2 C-),1.86(s,br,2H,-CH 2 -),2.22-2.30(m,4H,-CH 2 -),2.26(t,J=6.9Hz,4H,-...
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