A kind of [2]rotaxane based on pillar aromatics and its preparation and application
A technology for pillar aromatic hydrocarbons and rotaxanes, which is applied to [2]rotaxane and its preparation and application in catalytic coupling reactions, can solve problems such as less research on properties, and achieve the effect of improving catalytic efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0023] The preparation of pillararene [2]rotaxane, the synthetic route is as follows figure 1 shown.
[0024] The specific steps are: weigh 0.200g of guest G1 in a 50mL round-bottom flask, 1mmol (0.890g) of ethoxy column [5] arene, 5,5-dimethylcyclohexanedione (2.2eq. about 0.146g) and Malononitrile (2.2eq. about 0.066g) was dissolved in 10mL mixed solvent (EtOH:CHCl 3 =1:1), add 2 drops of piperidine dropwise. The reaction system was heated to reflux for 3h under magnetic stirring, and the reaction progress was detected by TCL. After the reaction was completed, the system was concentrated, and the crude product was separated by thin layer chromatography (DCM:MeOH=25:1). Recrystallization from ethanol, suction filtration to obtain light yellow solid R1.
[0025] Compounds R2, R3, R4, R5 were synthesized by the same method.
[0026] By hydrogen spectrum ( 1 H NMR), carbon spectrum ( 13 C NMR), high-resolution mass spectrometry (HR-ESI-MS), two-dimensional nuclear magneti...
Embodiment 2
[0036] Preparation of Pd Catalysts (Pd@R3) Based on Pillar Arene[2]rotaxane R3
[0037] Because there are two triazole groups on the [2] rotaxane axis prepared by the present invention, which can coordinate with Pd to form the [2] rotaxane hinge together to form a supramolecular polymer material with Pd , the new catalyst.
[0038] preparation process such as Figure 5 shown.
[0039]Specific steps: add 0.18g of column aromatic [2]rotaxane R3 and 5mL of acetonitrile to a 10mL round-bottomed flask, stir until R3 is completely dissolved, and then add AgNO 3 0.02g, continue to stir for 1 hour, filter out the solvent, wash twice with water to obtain catalyst Pd@R3.
[0040] The as-prepared catalyst Pd@R3 was characterized by transmission electron microscopy and energy dispersive analysis, as shown in Image 6 shown.
Embodiment 3
[0042] Catalyst Pd@R3 Catalytic Effect Test
[0043] The catalytic effect was tested by using the prepared new catalyst to catalyze the Suzuki-Miyaura coupling reaction.
[0044] The table below shows the catalysts Pd@R3 and Pd@3 based on rotaxane R3 and the precursor Pd(NO 3 ) 2 comparison of the catalytic effect.
[0045]
[0046] Reaction conditions: phenyl triflate (1.00 mmol), pyridine 4-boronic acid (1.50 mmol), K 2 CO 3 (2.00 mmol), catalyst (0.50 mol% Pd), DMF (5 mL), 100°C. Yields were determined by GC / MS (Agilent 1260).
[0047] From the above results, it can be seen that the catalyst of the present invention not only has good catalytic efficiency, but also can be recycled.
PUM
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