Dendrite self-assembled optical nonlinear chromophore as well as synthesis method and application thereof
An optical nonlinear and synthetic method technology, applied in the field of dendritic self-assembled optical nonlinear chromophore and its synthesis, can solve the problems of complex design, synthesis, polarization and cross-linking process of cross-linked electro-optical materials, and achieve improved Effects of long-term alignment stability, high EO coefficient, and high polarization efficiency
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Embodiment 1
[0078] An organic optical nonlinear chromophore based on a single-donor self-assembled structure, including H1-H3, its structure is shown in the appendix figure 2 , the chromophore H1-H3 shows good solubility in common organic solvents, such as ethyl acetate, ethanol and acetone.
[0079] Its preparation process includes the synthesis of chromophore H1-H3, and the steps are as follows:
[0080] S1. Under argon atmosphere and ice bath condition, add metallic sodium (32.03mmol, 0.74g) to the two-necked flask, dissolve with appropriate amount of ethanol, add 2-mercaptoethanol (32.03mmol, 2.26mL), add after 20mins Compound 1 (32.03 mmol, 4.94 g) was added after 1 h with compound 2a (32.03 mmol, 9.4 g) dissolved in an appropriate amount of ethanol, and the reaction was refluxed overnight at 65°C. , the eluent ratio is 1:10-1:5 (EA:PE), to obtain compound 3a (6.7g, 13.6mmol), the yield is: 42.5%, it is a red oily liquid;
[0081] MS(MALDI)(M + ,C 27 H 43 NO 3 SSi):calcd:489.7...
Embodiment 2
[0106] An organic optical nonlinear chromophore based on a single-donor self-assembled structure, including H1-H3, its structure is shown in the appendix Figure 4 , the chromophore H4 shows good solubility in common organic solvents, such as ethyl acetate, ethanol and acetone.
[0107] Its preparation process includes the synthesis of chromophore H4, and the steps are as follows:
[0108] P1. Under argon atmosphere, under ice bath condition, add metallic sodium (88.23mmol, 2.0g) to the two-necked flask, dissolve with appropriate amount of ethanol, add 2-mercaptoethanol (88.23mmol, 6.89g, 7.65mL), After 20 mins, compound 1 (132.35 mmol, 20.68 g) was added, and after 1 h, compound 2b (88.23 mmol, 23.23 g) dissolved in an appropriate amount of ethanol was added, and the reaction was refluxed overnight at 65 °C. Chromatography column, the eluent ratio is 1:8-1:3 (EA:PE), to obtain compound 3b (30.30 g, 65.9 mmol), yield: 74.7%, red oily liquid;
[0109] MS(MALDI)(M + ,C 26 H ...
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