Highly branched oily alkane polymer and its preparation method and application
A technology for oily alkanes and alkane mixtures, which can be used in the production of liquid hydrocarbon mixtures, lubricating compositions, and the petroleum industry. It can solve the problems of lower viscosity index of lubricating oils and unfavorable use of lubricating oils, and achieve high viscosity index and high degree of branching. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0070] Preparation of Ligand Compounds and Complexes
[0071] The present invention also provides the synthesis of the ligand compound of formula I, comprising the steps:
[0072] (a) C is obtained from the reaction of the corresponding diketone A with the amine compound B.
[0073] (b) Ligand I is obtained by reacting C with amine compound D.
[0074] Described compounds A, B, C, D have the following structural formula:
[0075]
[0076] In the reaction, it is necessary to add 0.001-100% of the corresponding catalyst that promotes the condensation reaction, such as acetic acid, p-toluenesulfonic acid, TiCl 4 , Orthosilicate, etc. Specifically, firstly, diketone A and amine B are mixed in an inert solvent, and activated by 0.001-100% acetic acid to generate monoimine C, and C continues to react with amine D to obtain the product represented by formula (I). The inert solvent can be all solvents commonly used in condensation reactions, including alcohols, aromatic hydroca...
Embodiment 1
[0132] Synthesis of Ligand L1a
[0133]
[0134] In a 100 mL egg-shaped bottle, add 3.644 g (20 mmol) of acenaphthylene quinone, add 40 mL of methanol, add 4.0 mL (20 mmol) of 2,6-diisopropylaniline, add 2 drops of anhydrous acetic acid, stir at room temperature, and follow the reaction by TLC to After completion, concentrated under reduced pressure, neutral alumina column chromatography, EA:PE=1:20-EA:PE=1:10 to obtain orange-yellow product monoimine with a yield of 60%. 1 H NMR (300MHz, CDCl 3 ): δ=8.21 (2H, m), 8.01 (1H, d), 7.82 (1H, t), 7.41 (1H, t), 7.27 (3H, s), 6.64 (1H, d), 2.84 (2H, m), 1.18 (6H, d), 0.90 (6H, d).
[0135] In a 100mL egg-shaped bottle, add 1.708g (5.0mmol) of monoimine, add 40mL of methanol, add 7.5mmol of aniline, add 2 drops of anhydrous acetic acid, stir at room temperature, follow the reaction by TLC to the end, concentrate under reduced pressure, neutral alumina Column chromatography, EA:PE=1:15 yields orange-yellow product L1a. 1 H NMR (...
Embodiment 2
[0137] Synthesis of Ligand L1b
[0138]
[0139] According to the synthetic method of ligand L1a in Example 1, 2,6-dichloroaniline was used to replace aniline in the second step, and other operating conditions were the same to obtain an orange solid. 1 H NMR (300MHz, CDCl 3 ): δ=8.32 (1H, d), 8.10 (1H, d), 7.96 (1.5H, m), 7.53 (2H, d), 7.41 (3H, m), 7.38 (2H, m), 6.91 (0.5 H, m), 6.58 (1H, t), 2.77 (2H, m), 1.29 (2H, d), 0.97 (10H, d), 13 C NMR (75MHz, CDCl3): δ=162.2, 157.8, 146.1, 133.1, 130.7, 127.5, 124.8, 124.4, 124.3, 123.39, 123.1, 122.7, 120.7, 77.4, 77.6, 28.5, 27.9, 23.5, 22.8. IR(KBr): v(cm -1 ) = 3052, 2960, 2923, 2865, 1674, 1640, 1602, 1463, 1433, 1242, 1077, 1033, 831, 779, 760, 730; C 30 H 26 Cl 2 N 2 (484.45): Anal.Calc.C 74.22, H 5.40, N 5.77; FoundC 73.99, H5.39, N 5.65.
PUM
| Property | Measurement | Unit |
|---|---|---|
| pour point | aaaaa | aaaaa |
| melting point | aaaaa | aaaaa |
| bromine number | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


