Ratio-type transition metal porphyran polymer luminescent oxygen sensing material
A technology based on porphyrin polymers and transition metals, applied in luminescent materials, material excitation analysis, fluorescence/phosphorescence, etc., can solve problems such as inaccurate oxygen measurement
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Embodiment 1
[0024] 1: Synthesis of meso-5,10,15,20-tetra(cyano)porphyrin
[0025] Firstly, p-cyanobenzaldehyde (1.31g, 10mmol) was dissolved in 20mL of propionic acid, and freshly distilled pyrrole (0.737g, 11mmol, 0.76mL) was dissolved in 10mL of propionic acid. Then, under the protection of nitrogen, the propionic acid solution of pyrrole was slowly added dropwise to the propionic acid solution of p-cyanobenzaldehyde, heated to 80° C. for 1 h, cooled to room temperature, filtered, and the filter cake was washed with absolute ethanol. Purification by column chromatography with dichloromethane as the eluent gave a dark purple solid.
[0026] 2: Synthesis of meso-5,10,15,20-tetrakis(cyano)porphyrin platinum complex
[0027] PtCl 2 (37.0mg, 0.14mmol) was added to 35mL of benzonitrile, heated to reflux for 4h, and the PtCl 2 After all dissolved in benzonitrile, meso-5,10,15,20-tetra(cyano)porphyrin (32.8 mg, 0.046 mmol) was added, and the reflux reaction was continued for 2 h. Benzonitri...
Embodiment 2
[0031] 1: Synthesis of meso-5,10,15,20-tetra(cyano)porphyrin
[0032] Firstly, p-cyanobenzaldehyde (1.31g, 10mmol) was dissolved in 20mL of propionic acid, and freshly distilled pyrrole (0.737g, 11mmol, 0.76mL) was dissolved in 10mL of propionic acid. Then, under the protection of nitrogen, the propionic acid solution of pyrrole was slowly added dropwise to the propionic acid solution of p-cyanobenzaldehyde, heated to 80° C. for 1 h, cooled to room temperature, filtered, and the filter cake was washed with absolute ethanol. Purification by column chromatography with dichloromethane as the eluent gave a dark purple solid.
[0033] 2: Synthesis of meso-5,10,15,20-tetra(cyano)porphyrin iridium complexes
[0034] IrCl 3 (41.7mg, 0.14mmol) was added to 35mL of benzonitrile, heated to reflux for 4h, and the IrCl 3 After all dissolved in benzonitrile, meso-5,10,15,20-tetra(cyano)porphyrin (32.8 mg, 0.046 mmol) was added, and the reflux reaction was continued for 2 h. Benzonitrile...
Embodiment 3
[0038] 1: Synthesis of meso-5,10,15,20-tetra(cyano)porphyrin
[0039] Firstly, p-cyanobenzaldehyde (1.31g, 10mmol) was dissolved in 20mL of propionic acid, and freshly distilled pyrrole (0.737g, 11mmol, 0.76mL) was dissolved in 10mL of propionic acid. Then, under the protection of nitrogen, the propionic acid solution of pyrrole was slowly added dropwise to the propionic acid solution of p-cyanobenzaldehyde, heated to 80° C. for 1 h, cooled to room temperature, filtered, and the filter cake was washed with absolute ethanol. Purification by column chromatography with dichloromethane as the eluent gave a dark purple solid.
[0040] 2: Synthesis of meso-5,10,15,20-tetra(cyano)porphyrin palladium complexes
[0041] PdCl 2 (24.8mg, 0.14mmol) was added to 35mL of benzonitrile, heated to reflux for 4h, and the PdCl2 After all dissolved in benzonitrile, meso-5,10,15,20-tetra(cyano)porphyrin (32.8 mg, 0.046 mmol) was added, and the reflux reaction was continued for 2 h. Benzonitrile...
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