Electrostatic complex fluorescent array sensor and its application
A technology of array sensors and complexes, applied in the direction of fluorescence/phosphorescence, instruments, scientific instruments, etc., can solve the problems of low sensitivity, high production cost, and poor reproducibility, and achieve high accuracy and sensitivity, low cost, and repeatability high effect
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Embodiment 1
[0040] Example 1. Synthesis of fluorescent polymer PPE1
[0041] The fluorescent macromolecular polymer used in the following examples is prepared according to the synthetic route shown in the following figure, by the method of the following steps:
[0042]
[0043] Monomer 1 (1.04 g, 2.35 mmol) and monomer 2 (2.09 g, 2.35 mmol) were dissolved in toluene / DIEA (7.2 mL / 4.9 mL), and Pd (PPh) was added 3 ) 2 Cl 2(4.95 mg, 7.05 μmol) and CuI (2.69 mg, 14.10 μmol) were stirred at room temperature for 24 h. Add saturated NH to the mixture 4 Cl solution and CHCl 3 , the aqueous layer was separated and washed with CHCl 3 extraction. Anhydrous MgSO 4 Dry, filter and remove the solvent under reduced pressure. The crude product was dissolved in a small amount of CHCl 3 , excess n-hexane was slowly added to precipitate, and the precipitation process was repeated three times to obtain compound 3 as a yellow-brown solid (2.63 g, 90%). Molecular weight M n Tested about 1.4x10 4...
Embodiment 2
[0045] Example 2. Synthesis of fluorescent polymer PPE 2
[0046] The fluorescent macromolecular polymer used in the following examples is prepared according to the synthetic route shown in the following figure, by the method of the following steps:
[0047]
[0048] Polymer 4 (25 mg, 0.082 mmol) was dissolved in N,N-dimethylethylenediamine (25 mL) and stirred at 50°C for 24 h. The solvent was removed under reduced pressure, and the crude product was washed with n-hexane. Drying in vacuo gave an orange solid as polymer 5 (52 mg, 0.077 mmol, 94%). 1 H NMR (300 MHz, CDCl3): δ 7.14 (s, 2H), 4.52 (s, 4H), 3.31 (s, 4H), 2.81 (s, 4H), 2.17 (s, 12H). 13 C NMR (300MHz, CDCl3): δ 168.97, 157.57, 118.45, 113.49, 92.94, 90.67, 68.57, 58.10, 44.97, 36.44.
[0049] Polymer 5 (40 mg, 0.1 mmol) was dissolved in dichloromethane (25 mL) and iodomethane (15 mL) was added. Stir overnight at room temperature. The solvent was removed under reduced pressure, washed with hexane, and dried in...
Embodiment 3
[0050] Example 3. Synthesis of fluorescent polymer PPE 3
[0051] The fluorescent macromolecular polymers used in the following examples are prepared according to the synthetic route diagram shown in the attached figure by the following steps:
[0052]
[0053] Monomer 6 (820 mg, 1.00 mmol) and monomer 7 (347 mg, 1.05 mmol) were dissolved in dichloromethane / DIEA / triethylamine (2mL / 2mL / 1mL), and Pd (PPh) was added 3 ) 2 Cl 2 (1.4 mg, 2 μmol) and CuI (0.4 mg, 2 μmol) were stirred at room temperature for 24 h. Polymer 8 (70 mg, 0.082 mmol) was dissolved in N,N-dimethylethylenediamine (25 mL) and stirred at 50°C for 24 h. The solvent was removed under reduced pressure, and the crude product was washed with n-hexane. Drying in vacuo gave an orange solid as polymer 9 (89.4 mg, 0.077 mmol, 94%). Polymer 9 (40 mg, 0.0344 mmol) was dissolved in dichloromethane (25 mL) and iodomethane (15 mL) was added. Stir overnight at room temperature. The solvent was removed under reduced ...
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