[2]rotaxane based on pillararene as well as preparation and application thereof
A technology for pillar aromatics and rotaxanes, applied in [2] rotaxanes 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
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Embodiment 1
[0023] The preparation of pillar arene [2] rotaxane, the synthetic route is as figure 1 shown.
[0024] The specific steps are: in a 50mL round bottom flask, weigh 0.200g of guest G1, 1mmol (0.890g) of ethoxypillar[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 3 h under magnetic stirring, and the progress of the reaction was detected by TCL. After the reaction, the system was concentrated, and the crude product was separated by thin-layer chromatography (DCM:MeOH=25:1). Recrystallize with ethanol, and filter with suction to obtain a light yellow solid R1.
[0025] Compounds R2, R3, R4, and 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 NMR (2DNOESY) and theo...
Embodiment 2
[0036] Preparation of Pd Catalyst (Pd@R3) Based on Pillararene[2]rotaxane R3
[0037] Since there are two triazole groups on the [2] rotaxane axis prepared by the present invention based on pillar arene, it can be coordinated with Pd to hinge the [2] rotaxane to form a supramolecular polymer material with Pd , the new catalyst.
[0038] The preparation process is as Figure 5 shown.
[0039]Specific steps: Add 0.18g of columnarene[2]rotaxane R3 and 5mL of acetonitrile into a 10mL round bottom flask, stir until R3 is completely dissolved, then add AgNO 3 0.02g, continue to stir for 1 hour, filter out the solvent, wash twice with water to obtain the catalyst Pd@R3.
[0040] The as-prepared catalyst Pd@R3 was characterized by transmission electron microscopy and energy spectrum analysis, as shown in Figure 6 shown.
Embodiment 3
[0042] Catalyst Pd@R3 catalytic effect test
[0043] The catalytic effect was detected by using the prepared new catalyst to catalyze the Suzuki-Miyaura coupling reaction.
[0044] The following table is the catalysts Pd@R3 and Pd@3 based on rotaxane R3 and the precursor Pd(NO 3 ) 2 comparison of catalytic effects.
[0045]
[0046] Reaction conditions: phenyl triflate (1.00mmol), pyridinium 4-boronate (1.50mmol), 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] It can be seen from the above results that the catalyst of the present invention not only has good catalytic efficiency, but also can be recycled.
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