Triarylamine-containing polyurethane as well as preparation method and application thereof
A technology of triarylamine and polyurethane, which is applied in the field of polyurethane and its preparation, can solve the problems of low solubility, low photochromic response sensitivity, and poor processability, and achieve good electrochromic performance
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specific Embodiment approach 1
[0066] Specific embodiment one: this embodiment is a kind of structural formula of the polyurethane containing triarylamine is: Wherein, described Ar is: The R is: The value range of n is 1≤n≤100, and n is an integer.
[0067] The advantage of this implementation mode:
[0068] 1. The polyurethane containing triarylamine prepared by this embodiment overcomes the disadvantage that polyurethane is difficult to dissolve in general organic solvents in the past. The polyurethane containing triarylamine utilizes the introduction of large groups of triphenylamine to improve the solubility of the entire polymer, making the polyurethane containing triarylamine Polyurethane is soluble in most organic solvents; at the same time, the CO-NH structure formed by polyurethane is connected to the benzene ring, and the color changes after oxidation, and can undergo reversible changes accompanied by reversible color changes;
[0069] 2. Under a nitrogen atmosphere, the polyurethane conta...
specific Embodiment approach 2
[0072] Specific embodiment two: present embodiment is a kind of preparation method of the polyurethane containing triarylamine is finished according to the following steps:
[0073] 1. Synthesis of monoamine monomer:
[0074] ①. Under a nitrogen atmosphere, dissolve diphenylamine in anhydrous dimethyl sulfoxide, then add p-fluoronitrobenzene and sodium hydride, then heat and reflux at a temperature of 150°C to 160°C for 36h to 48h, and then use Distilled water at a temperature of 0°C to 5°C precipitates the product A, and then uses acetonitrile to recrystallize the product A, and then dries at a temperature of 40°C to 50°C for 10h to 12h to obtain a triphenylamine nitro compound;
[0075] The volume ratio of the mass of diphenylamine described in step 1 to anhydrous dimethyl sulfoxide is (0.1g~0.5g): 10mL;
[0076] The mol ratio of the diphenylamine described in step 1. and p-fluoronitrobenzene is 1:1;
[0077] Step 1. The mass ratio of diphenylamine and sodium hydride descr...
specific Embodiment approach 3
[0106]Specific embodiment three: the difference between this embodiment and specific embodiment two is: the structure of the isocyanate monomer obtained in step three is Others are the same as in the second embodiment.
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