NIR-II conjugated nano particles, and preparation method and application thereof
A nanoparticle and near-infrared technology, applied in wave energy or particle radiation treatment materials, pharmaceutical formulations, medical preparations with inactive ingredients, etc., can solve problems such as limiting large-scale preparation and clinical transformation, and achieve good clinical transformation possibilities. The effect of stability, mild reaction system and stable properties
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[0045] Example 1: Conjugated small molecules
[0046] Dibromobenzobisthiadiazole (88.0mg, 0.25mmol), 4-tert-butyl-N-(4-tert-butylphenyl)-N-(4-(5'-trimethylstannyl) -(2,2'-Bithienyl)-5-phenyl)aniline (342.3mg, 0.50mmol) and bis(triphenylphosphine) palladium dichloride (8.77mg, 0.0125mmol) dissolved in 30mL dry toluene Reflux for 24 hours in an inert atmosphere, and finally silica gel column chromatography (eluent is dichloromethane) to obtain near-infrared two-zone conjugated small molecules with a yield of 60%.
[0047] The obtained near-infrared two-region conjugated small molecules were characterized by proton nuclear magnetic resonance spectroscopy and MALDI-TOF mass spectrometry, and the results are as attached figure 1 And figure 2 Shown.
Example Embodiment
[0048] Example 2: Conjugated small molecules
[0049] Dibromobenzobisthiadiazole (88.0mg, 0.25mmol), 4-tert-butyl-N-(4-tert-butylphenyl)-N-(4-(5'-trimethylstannyl) -(2,2'-Bithienyl)-5-phenyl)aniline (342.3mg, 0.50mmol) and tetrakis(triphenylphosphine)palladium (14.4mg, 0.0125mmol) dissolved in 30mL dry toluene, inert Reflux in the atmosphere for 24 hours, and finally silica gel column chromatography (eluent is dichloromethane) to obtain near-infrared two-region conjugated small molecules with a yield of 65%.
Example Embodiment
[0050] Example 3: Conjugated small molecules
[0051] Dibromobenzobisthiadiazole (88.0mg, 0.25mmol), 4-tert-butyl-N-(4-tert-butylphenyl)-N-(4-(5'-trimethylstannyl) -(2,2'-Bithienyl)-5-phenyl)aniline (342.3mg, 0.50mmol) and bis(dibenzylideneacetone)palladium (7.19mg, 0.0125mmol) were dissolved in 30mL of dry toluene, Reflux for 24 hours in an inert atmosphere, and finally silica gel column chromatography (eluent is dichloromethane) to obtain near-infrared two-region conjugated small molecules with a yield of 61%.
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