Titanium catalyst as well as preparation method and application of titanium catalyst
A titanium-based catalyst and catalyst technology, which is applied in the direction of chemical instruments and methods, physical/chemical process catalysts, titanium organic compounds, etc., can solve the problem that polycarbonate materials are difficult to popularize in the fields of food and medical packaging, and cannot be applied to actual industries. Production and other issues, to achieve the effect of good selectivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0064] The present invention also provides a preparation method of titanium series catalyst, comprising:
[0065] 1) reacting the aldehyde compound represented by formula (VI-a) with the diamine represented by formula (VI-b) to obtain a tetradentate bis-Schiff base ligand;
[0066] Formula (VI-a), Formula (VI-b);
[0067] Among them, R 1 C1-C20 alkylene, C1-C20 alkyleneoxy, C6-C20 arylene, C6-C20 substituted arylene;
[0068] R 2 , R 3 , R 4 independently selected from: H, C1-C20 alkyl, C1-C20 alkoxy or fluorine-substituted C1-C20 alkyl,
[0069] or R 2 and R 3 and their adjacent carbons together form a closed ring;
[0070] or R 3 and R 4 and their adjacent carbons together form a closed ring;
[0071] 2) Combine tetradentate double Schiff base ligands with TiCl 3 .(THF) 3 React in the presence of a base to obtain a titanium-based catalyst.
[0072] According to the present invention, the aldehyde compound shown in formula (VI-a) is reacted with the diamine ...
Embodiment 1
[0084] Example 1: Trivalent titanium tetrahydrofuran complex TiCl 3 .(THF) 3 preparation of
[0085] Add 5.0g (25mmol) purple 3TiCl to the 100mL single-necked flask 3 .AlCl 3 , with 4 mL of refined toluene, put it into a dry ice-acetone bath at -78 ° C, and slowly drop into 5 mL of refined THF. After the dropwise addition, the system was slowly heated to 70°C and refluxed for 20 hours. After the reflux was completed, it was cooled to room temperature and filtered. The filter residue was washed three times with refined n-hexane, and the residual solvent was removed under reduced pressure to obtain 7.59 g of a light blue solid product. The yield was 82%.
[0086] By elemental analyzer, to the TiCl prepared in embodiment 1 3 .(THF) 3 Carry out analysis, its element analysis result is: C, 38.55, H, 6.64; Actual calculation result is: C, 38.68, H, 6.50; Visible, the embodiment preparation is indeed TiCl 3 .(THF) 3 .
Embodiment 2
[0087] Example 2: Preparation of complexes with the structure of formula (VII).
[0088] 4.68 g of 3,5-di-tert-butyl salicylaldehyde (20 mmol) was dissolved in 100 mL of dry ethanol, and 1.08 g of 1,2-phenylenediamine (10 mmol) was dissolved in 20 mL of dry ethanol. Then, under the condition of stirring, the ethanol solution of 1,2-o-phenylenediamine was added dropwise to the ethanol solution of 3,5-di-tert-butyl water aldehyde, heated to reflux and stirred for 14 hours, then cooled the reaction mixture to room temperature, rotated Volatile substances were removed by evaporation to obtain a solid, which was recrystallized from ethanol and dried in vacuo to obtain 5.05 g of yellow needle-shaped tetradentate bis-Schiff base ligand III with a yield of 93%.
[0089] Tetradentate double Schiff base ligand III;
[0090] Dissolve the above-mentioned tetradentate bis-Schiff base ligand III in refined 20mL THF, cool to 0°C and add 4 equivalents of NaH (60% dispersed in mineral oil),...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight distribution | aaaaa | aaaaa |
molecular weight distribution | aaaaa | aaaaa |
molecular weight distribution | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com