Quinoline unit structure-based 5/6/6 ring-fused tetradentate cyclometalated platinum (II) complex phosphorescent material and application thereof
A phosphorescent material and unit structure technology, applied in the direction of luminescent materials, compounds containing elements of Group 8/9/10/18 of the periodic table, platinum group organic compounds, etc., can solve the reduction of chemical stability and thermal stability of complexes , low phosphorescence quantum efficiency, easy distortion of bidentate ligands, etc., to achieve the effects of improving chemical stability and thermal stability, suppressing non-radiative transitions, and improving quantum efficiency
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[0040] The content of the present invention will be described in detail below. The description of the constituent elements described below may be based on representative embodiments or specific examples of the present invention, but the present invention is not limited to such embodiments or specific examples.
[0041] The compounds contained in the 5 / 6 / 6 asymmetric tetracyclic metal platinum(II) complex phosphorescent material based on the quinoline unit structure of the present invention have the structure of the following general formula (1).
[0042]
[0043]The synthetic route of the compound in the general formula (1) is as follows:
[0044]
[0045] Specific examples of the phosphorescent material of the present invention represented by the following general formula (1) are illustrated below, however, it is not to be construed as limiting the present invention.
[0046] Unless otherwise stated, all commercial reagents involved in the following experiments were pu...
Embodiment 1
[0047] Example 1: The synthesis route of tetracyclic metal platinum (II) complex phosphorescent material Pt1 is as follows:
[0048]
[0049] (1) Synthesis of intermediate 1-N: Into a 100mL three-neck flask with a magnetic rotor, add 8-hydroxyquinoline (5.00g, 34.5mmol, 1.00 equivalent), 40mL of N,N-dimethylformamide, Then it was placed in a low-temperature stirred tank, and after the temperature dropped, slowly added sodium hydride (1.38g, 34.5mmol, 1.00 equivalent) with a mass fraction of 60%, and added methyl iodide (5.14g, 36.3mmol, 1.05 equivalent), reacted overnight. The reaction mixture was quenched with ethanol, and after the solvent was distilled off under reduced pressure, it was extracted three times with ethyl acetate, the organic phases were combined, dried with anhydrous sodium sulfate, and the resulting crude product was separated and purified by silica gel column chromatography, and the eluent (petroleum ether / acetone=2:1), 4.76 g of black-red liquid was o...
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