A trans-octadecaborane derivative and its preparation method and application
A technology of octadecaborane and its derivatives, which is applied in the field of trans-octadecaborane derivatives and its preparation to achieve excellent aggregation-induced luminescent properties
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[0029] The preparation method of the above-mentioned trans-octadecaborane derivatives. Its preparation route is:
[0030]
[0031] The specific preparation process includes the following steps: 1) react isoquinoline and trans-octadecaborane in a solvent to obtain isoquinoline-substituted anti-B 18 h 22 Compound crude product; 2) anti-B substituted with isoquinoline 18 h 22 The crude compound is purified and obtained.
Embodiment 1
[0033] This embodiment provides a preparation method of trans-octadecaborane derivatives, which specifically includes the following steps:
[0034] 1) Add isoquinoline (0.505ml, 4.297mmol) dropwise into 20ml of dry benzene solution, and stir on a magnetic stirrer for 10min to disperse evenly, and record it as solution A; then weighed trans-18-boron alkane anti-B 18 h 22 (200mg, 0.923mmol) was poured into a 100ml round bottom flask, and 60ml of dry benzene solution was added, stirred on a magnetic stirrer for about 15min until anti-B 18 h 22 Completely dissolved, recorded as B solution; slowly drop A solution into B solution, the solution immediately turned yellow, and with the continuous increase of A solution, the yellow color continued to deepen to orange yellow, and the mixture of A and B was recorded as C Solution; under the protection of nitrogen atmosphere, heat and stir the C solution to reflux the benzene solution. During this process, a yellow precipitate is formed...
Embodiment 2
[0042] This embodiment provides a preparation method of trans-octadecaborane derivatives. The difference from Example 1 is that isoquinoline and trans-octadecaborane are directly put into the dry benzene solution in sequence, and Heating and stirring the C solution under protection makes the benzene solution reflux, and other conditions are the same as in Example 1. Finally, the reaction time of step 1) is prolonged by at least 2 times.
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