Polyimide derivatives containing bis-tetra-tert-butylaniline structure and naphthalene imide fluorescent group, preparation method and application thereof
A technology of tert-butyl aniline and tert-butyl phenyl is applied to polyimide derivatives containing bis-tetra-tert-butyl aniline structure and naphthalimide fluorescent group and the fields of preparation and application thereof, and can solve the problem of Poor film strength and transparency, high processing difficulty, poor solubility, etc., to achieve good wetting ability, excellent mechanical properties, and the effect of increasing solubility
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specific Embodiment approach 1
[0033] Specific embodiment one: In this embodiment, the structural formula of polyimide derivatives containing bis-tetra-tert-butylaniline structure and naphthalimide fluorescent group is as follows:
[0034] ,
[0035] In the formula, n is an integer of 3-10.
[0036] This implementation mode expands the application range of electrochromic materials. The aromatic polyimide polymer material has aroused great interest of scientific researchers due to its excellent heat resistance and mechanical properties. Introducing triarylamine groups with disruptive stacking properties into the polyimide structure can not only maintain the high thermal stability of the original polyimide, but also increase its solubility and enhance the film-forming ability, which is not only conducive to the manufacture of large The thin film electrochromic device of the area also provides the electroactive center to facilitate the processing and application of the electrochromic device; the polyimide d...
specific Embodiment approach 2
[0038] Specific embodiment two: the preparation method of the polyimide derivative containing bis-tetra-tert-butylaniline structure and naphthalimide fluorescent group in this embodiment is as follows: 1. Synthesizing polyimide derivatives containing bis-tetra-tert-butylaniline structure Imine precursor
[0039] Mix bis-tetra-tert-butylaniline diamine monomer, 3,3'-dihydroxyaniline, hexafluorodianhydride and solvent N-methylpyrrolidone, stir and reflux for 5-10 hours at room temperature, and the stirring speed is 800r / min~ 900r / min, then add acetic anhydride and catalyst pyridine, heat up to 100-150°C, stir and reflux for 10-15h, pour into methanol after cooling, filter, and vacuum-dry the obtained solid phase to obtain polyimide front body;
[0040] 2. Preparation of polyimide derivatives containing bis-tetra-tert-butylaniline structure and naphthalimide fluorescent group
[0041] Add polyimide precursor, solvent N-methylpyrrolidone, naphthalimide derivatives containing hyd...
specific Embodiment approach 3
[0048] Specific embodiment three: the difference between this embodiment and specific embodiment two is: the molar ratio of bis-tetra-tert-butylaniline diamine monomer, 3,3'-dihydroxyaniline, and hexafluorodianhydride described in step one is 1:1:2. It is the same as the second embodiment.
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