Application of 5-methylpyridinetetrazole tetranuclear copper [I] complex in stimulus-responsive luminescent color-changing material
A picoline tetrazolium and stimuli-responsive technology, which is applied in the field of stimuli-responsive luminescent color-changing new material synthesis, can solve the problem of less luminescent color-changing materials and the like
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Embodiment 1
[0038] Under an argon atmosphere, [Cu[CH 3 EN] 4 ][ClO 4 ] (29.4 mg, 0.090 mmol), N,N-bis[diphenylphosphoryl]amide (34.7 mg, 0.090 mmol) and 5-[5-methyl-2-pyridyl]tetrazole (7.3 mg, 0.045 mmol) in 10 mL of dichloromethane at room temperature for 3 hours, then add sodium hydroxide (1.8 mg, 0.045 mmol) to the reaction solution, continue stirring for 1 hour at room temperature, and then use a rotary evaporator to depressurize the solvent Evaporate to dryness, and recrystallize with a mixed solvent of N,N-dimethylformamide (1 mL)-diethyl ether (10 mL) [volume ratio is 1:10]. The light yellow crystalline product obtained by recrystallization was filtered, washed 3-4 times with 10 mL of diethyl ether, and dried in vacuo to obtain a light yellow solid product (37.1 mg, 0.016 mmol) with a yield of 71%.
[0039] Elemental analysis calculated value (C 110 H 96 Cl 2 Cu 4 N 14 O 8 P 8 ) is (%): C 57.07, H 4.18, N 8.47; found values: C 57.09, H 4.19, N 8.45.
[0040] X-ray singl...
Embodiment 2
[0043] Under argon atmosphere, copper perchlorate hexahydrate [Cu[ClO 4 ] 2 ·6H 2 O] (15.6 mg, 0.042 mmol) and excess copper powder (16.5 mg, 0.260 mmol) were stirred in 5 mL of acetonitrile at room temperature for 30 minutes, and then N,N-bis[diphenylphosphoryl]amide (32.4 mg, 0.084 mg) was added. mmol) in 10 mL of dichloromethane solution, continue to stir and react for 1 hour, add 5-[5-methyl-2-pyridyl]tetrazolium ligand (6.8 mg, 0.042 mmol), continue to stir and react for 2 hours at room temperature, Then, sodium hydroxide (1.7 mg, 0.042 mmol) was added to the reaction solution, and the reaction was continued to stir at room temperature for 1 hour. After filtration, the solvent was evaporated to dryness under reduced pressure with a rotary evaporator, and N,N-dimethylformamide ( 1mL)-diethyl ether (10mL) mixed solvent [volume ratio is 1:10] for recrystallization. The light yellow crystalline product obtained by recrystallization was filtered, washed 3-4 times with 10 mL...
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