Platinum complex
A technology of platinum complexes and complexes, which is applied in the direction of platinum group organic compounds, platinum organic compounds, compounds containing group 8/9/10/18 elements of the periodic table, etc., and can solve the problems of efficiency reduction, phosphorescence quenching, Efficiency roll-off and other issues, to achieve the effect of convenient design and production, simple preparation method and high yield
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Embodiment 1
[0059] Embodiment 1, the synthesis of complex PtOPN-001:
[0060]
[0061] Platinum salt K2PtCl4 (0.415g, 1mmol) and 2-(4-trifluoromethyl) phenylpyridine (2.5mmol, 0.475g) were added to a mixed solvent of 2-ethoxyethanol and water (3:1, v / v). The reaction system was stirred and reacted at 80° C. for 16 hours, and the precipitate was the platinum dimer bridged complex. Take the platinum dimer bridged complex (0.33mmol, 0.3g) and Kfpip (0.99mmol, 0.53g) into 2-ethoxyethanol solvent, react at 80°C for 16 hours, cool, remove the solvent under reduced pressure, and Column chromatography (silica gel column, eluent: CH2Cl2 / petroleum ether 1:2 (v / v)), the obtained yellow powder is PtOPN-001.
[0062] Yield: 25.0%.1H NMR (500MHz, CDCl3) δ9.13-8.99 (m, 1H), 7.91-7.87 (m, 8H), 7.78 (t, J=7.83Hz, 1H), 7.37-7.34 ( m,10H),7.13-7.07(m,2H),6.85(ddd,J=2.37,9.24,11.84Hz,1H).MALDI-TOF,m / z:905.379[M].
[0063]
Embodiment 2
[0064] Embodiment 2, the synthesis of complex PtOPN-007:
[0065]
[0066] Use the same operation method as in Implementation 1, just replace Kfpip with Ktfmpip to get PtOPN-007. Yield: 25.0%. MALDI-TOF, m / z: 1105.603[M].
[0067]
Embodiment 3
[0068] Embodiment three, the synthesis of complex PtOPN-010:
[0069]
[0070] Adopt the same operation mode as in the first implementation, just replace Kfpip with Na5fpip to obtain PtOPN-007. Yield: 10.0%. MALDI-TOF, m / z: 1193.4778[M].
[0071]
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