A kind of si-o-si chain bridged n-heterocyclic carbene platinum complex and its preparation method and application
A technology of si-o-si and complexes, which is applied in the direction of platinum organic compounds, platinum group organic compounds, compounds of group 4/14 elements of the periodic table, etc., to achieve easy separation, design, high selectivity, and compatibility good sex effect
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Embodiment 1
[0023] (1) Add 6.2g of butylimidazole and 5.0g of 1,3-dichloromethyltetramethylsiloxane (molar ratio 2:1) into a 250mL three-necked flask and add it to a flask equipped with magnetic stirring, heating and condensing In the reactor, add toluene as a solvent, stir and react at 110° C. for 24 h, separate and purify to obtain the [Si-O-Si] chain-bridged carbene precursor.
[0024] (2) Take 2.74g (0.005mol) of the above-mentioned ionic liquid, 1.68g (0.015mol) of potassium tert-butoxide, and 50mL of anhydrous tetrahydrofuran as a solvent. After reacting for 1h under the protection of nitrogen, add 9.75g of Karstedt's catalyst (Pt content 1.95g , 0.01mol), stirred at room temperature for 72h, separated and purified to obtain [Si-O-Si] chain-bridged N-heterocyclic carbene platinum (0) complex 1.
Embodiment 2
[0026] Using the method in Example 1, butylimidazole is replaced with phenylimidazole in step (1), the molar ratio of phenylimidazole to 5.0 g of 1,3-dichloromethyltetramethylsiloxane is 2:1, and Add toluene as a solvent into a reactor equipped with magnetic stirring, heating device and condensing device, stir and react at 120°C for 12 hours, separate and purify to obtain [Si-O-Si] chain-bridged carbene precursor. Step (2) prepare Si-O-Si] chain bridged N-heterocyclic carbene platinum (0) complex 2.
Embodiment 3
[0028] Adopt the method among the embodiment 1, in step (1), replace butylimidazole with 2,4,6-trimethylphenylimidazole, make the N-heterocyclic carbene platinum of Si-O-Si] chain bridging ( 0) Complex 3.
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